Chemicals

Showing 28201–28350 of 41137 results

  • N-Arachidonoyl dopamine-d8 contains eight deuterium atoms at the 5, 6, 8, 9, 11, 12, 14, and 15 positions. It is intended for use as an internal standard for the quantification of N-arachidonoyl dopamine by GC- or LC-mass spectrometry. Several different arachidonoyl amino acids, including NADA, have been isolated and characterized from bovine brain.{9589} NADA is the amide of the neurotransmitter dopamine and arachidonic acid. NADA is a CB1-selective cannabinoid agonist, inducing the typical tetrad of hypothermia, analgesia, catalepsy, and hypomotility in rats which exceeds that of anandamide (AEA).{9213} NADA is a full agonist at the vanilloid receptor 1, but is inactive on the dopaminergic D1 and D2 receptors. NADA is also a potent inhibitor (IC50 = 0.25 µM) of the proliferation of MCF-7 breast carcinoma cells. Recent reports of NADA’s endothelium-dependent vasodilation indicate that some of its cannabinergic activities antagonized by SR141716A may be non-CB1/CB2 dependent.{11224}  

     

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    SKU:10007431 - 1 mg

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  • N-Arachidonoyl dopamine-d8 contains eight deuterium atoms at the 5, 6, 8, 9, 11, 12, 14, and 15 positions. It is intended for use as an internal standard for the quantification of N-arachidonoyl dopamine by GC- or LC-mass spectrometry. Several different arachidonoyl amino acids, including NADA, have been isolated and characterized from bovine brain.{9589} NADA is the amide of the neurotransmitter dopamine and arachidonic acid. NADA is a CB1-selective cannabinoid agonist, inducing the typical tetrad of hypothermia, analgesia, catalepsy, and hypomotility in rats which exceeds that of anandamide (AEA).{9213} NADA is a full agonist at the vanilloid receptor 1, but is inactive on the dopaminergic D1 and D2 receptors. NADA is also a potent inhibitor (IC50 = 0.25 µM) of the proliferation of MCF-7 breast carcinoma cells. Recent reports of NADA’s endothelium-dependent vasodilation indicate that some of its cannabinergic activities antagonized by SR141716A may be non-CB1/CB2 dependent.{11224}  

     

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  • N-Arachidonoyl dopamine-d8 contains eight deuterium atoms at the 5, 6, 8, 9, 11, 12, 14, and 15 positions. It is intended for use as an internal standard for the quantification of N-arachidonoyl dopamine by GC- or LC-mass spectrometry. Several different arachidonoyl amino acids, including NADA, have been isolated and characterized from bovine brain.{9589} NADA is the amide of the neurotransmitter dopamine and arachidonic acid. NADA is a CB1-selective cannabinoid agonist, inducing the typical tetrad of hypothermia, analgesia, catalepsy, and hypomotility in rats which exceeds that of anandamide (AEA).{9213} NADA is a full agonist at the vanilloid receptor 1, but is inactive on the dopaminergic D1 and D2 receptors. NADA is also a potent inhibitor (IC50 = 0.25 µM) of the proliferation of MCF-7 breast carcinoma cells. Recent reports of NADA’s endothelium-dependent vasodilation indicate that some of its cannabinergic activities antagonized by SR141716A may be non-CB1/CB2 dependent.{11224}  

     

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  • N-Arachidonoyl taurine is an arachidonoyl amino acid.{16245} It is oxygenated by 12(S)- and 15(S)-lipoxygenase and is converted to 12-HETE-taurine (12-HETE-T) in murine resident peritoneal macrophages.{46067} N-Arachidonoyl taurine is an activator of the transient receptor potential vanilloid (TRPV) channels TRPV1 and TRPV4 (EC50s = 28 and 21 µM, respectively).{16245} It increases calcium flux in HIT-T15 pancreatic β-cells and INS-1 rat islet cells when used at a concentration of 10 µM and increases insulin secretion from 832/13 INS-1 pancreatic β-cells.{46068} The levels of N-arachidonoyl taurine are changed in mouse brain following administration of Δ9-tetrahydrocannabinol (Δ9-THC).{46069}  

     

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  • N-Arachidonoyl taurine is an arachidonoyl amino acid.{16245} It is oxygenated by 12(S)- and 15(S)-lipoxygenase and is converted to 12-HETE-taurine (12-HETE-T) in murine resident peritoneal macrophages.{46067} N-Arachidonoyl taurine is an activator of the transient receptor potential vanilloid (TRPV) channels TRPV1 and TRPV4 (EC50s = 28 and 21 µM, respectively).{16245} It increases calcium flux in HIT-T15 pancreatic β-cells and INS-1 rat islet cells when used at a concentration of 10 µM and increases insulin secretion from 832/13 INS-1 pancreatic β-cells.{46068} The levels of N-arachidonoyl taurine are changed in mouse brain following administration of Δ9-tetrahydrocannabinol (Δ9-THC).{46069}  

     

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  • N-Arachidonoyl taurine is an arachidonoyl amino acid.{16245} It is oxygenated by 12(S)- and 15(S)-lipoxygenase and is converted to 12-HETE-taurine (12-HETE-T) in murine resident peritoneal macrophages.{46067} N-Arachidonoyl taurine is an activator of the transient receptor potential vanilloid (TRPV) channels TRPV1 and TRPV4 (EC50s = 28 and 21 µM, respectively).{16245} It increases calcium flux in HIT-T15 pancreatic β-cells and INS-1 rat islet cells when used at a concentration of 10 µM and increases insulin secretion from 832/13 INS-1 pancreatic β-cells.{46068} The levels of N-arachidonoyl taurine are changed in mouse brain following administration of Δ9-tetrahydrocannabinol (Δ9-THC).{46069}  

     

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  • N-Arachidonoyl taurine is an arachidonoyl amino acid.{16245} It is oxygenated by 12(S)- and 15(S)-lipoxygenase and is converted to 12-HETE-taurine (12-HETE-T) in murine resident peritoneal macrophages.{46067} N-Arachidonoyl taurine is an activator of the transient receptor potential vanilloid (TRPV) channels TRPV1 and TRPV4 (EC50s = 28 and 21 µM, respectively).{16245} It increases calcium flux in HIT-T15 pancreatic β-cells and INS-1 rat islet cells when used at a concentration of 10 µM and increases insulin secretion from 832/13 INS-1 pancreatic β-cells.{46068} The levels of N-arachidonoyl taurine are changed in mouse brain following administration of Δ9-tetrahydrocannabinol (Δ9-THC).{46069}  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-3-hydroxy-γ-aminobutyric acid (NAG-3H-ABA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly; Item No. 90051) was further characterized and found to suppress formalin-induced pain in rats. NAG-3H-ABA was also found in rat brain by LC-MS techniques, but has not been fully characterized to date. Most arachidonoyl amino acids are poor ligands for the CB1 receptor.  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-3-hydroxy-γ-aminobutyric acid (NAG-3H-ABA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly; Item No. 90051) was further characterized and found to suppress formalin-induced pain in rats. NAG-3H-ABA was also found in rat brain by LC-MS techniques, but has not been fully characterized to date. Most arachidonoyl amino acids are poor ligands for the CB1 receptor.  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-3-hydroxy-γ-aminobutyric acid (NAG-3H-ABA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly; Item No. 90051) was further characterized and found to suppress formalin-induced pain in rats. NAG-3H-ABA was also found in rat brain by LC-MS techniques, but has not been fully characterized to date. Most arachidonoyl amino acids are poor ligands for the CB1 receptor.  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-3-hydroxy-γ-aminobutyric acid (NAG-3H-ABA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly; Item No. 90051) was further characterized and found to suppress formalin-induced pain in rats. NAG-3H-ABA was also found in rat brain by LC-MS techniques, but has not been fully characterized to date. Most arachidonoyl amino acids are poor ligands for the CB1 receptor.  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-L-alanine (NALA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly) was further characterized and found to suppress formalin-induced pain in rats. NALA may have activity at cannabinoid receptor and/or VR1, but has not been fully characterized to date.  

     

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    SKU:90065 - 10 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-L-alanine (NALA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly) was further characterized and found to suppress formalin-induced pain in rats. NALA may have activity at cannabinoid receptor and/or VR1, but has not been fully characterized to date.  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-L-alanine (NALA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly) was further characterized and found to suppress formalin-induced pain in rats. NALA may have activity at cannabinoid receptor and/or VR1, but has not been fully characterized to date.  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl-L-alanine (NALA), have been isolated and characterized from bovine brain.{9589} The glycine congener (NAGly) was further characterized and found to suppress formalin-induced pain in rats. NALA may have activity at cannabinoid receptor and/or VR1, but has not been fully characterized to date.  

     

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    SKU:90065 - 50 mg

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  • Arachidonoyl amides of both amino acids and neurotransmitters such as dopamine have been previously reported in the literature.{9213} N-Arachidonoyl-L-serine (ARA-S) is one such recently isolated endocannabinoid with an unusual activity profile. ARA-S does not bind to central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors or vanilloid receptor 1 (VR1). Like cannabidiol, ARA-S (5 mg/kg) antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model.{11984} However, similar to Abn-CBD, ARA-S relaxes isolated rat mesenteric arteries and abdominal aorta as well as increases phosphorylation of Akt and mitogen-activated protein kinase (MAPK) in HUVEC.{14066} The precise mechanisms of action by ARA-S and Abn-DBD in various vascular preparations appears to be different and requires further investigation.  

     

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    SKU:10005455 - 1 mg

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  • Arachidonoyl amides of both amino acids and neurotransmitters such as dopamine have been previously reported in the literature.{9213} N-Arachidonoyl-L-serine (ARA-S) is one such recently isolated endocannabinoid with an unusual activity profile. ARA-S does not bind to central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors or vanilloid receptor 1 (VR1). Like cannabidiol, ARA-S (5 mg/kg) antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model.{11984} However, similar to Abn-CBD, ARA-S relaxes isolated rat mesenteric arteries and abdominal aorta as well as increases phosphorylation of Akt and mitogen-activated protein kinase (MAPK) in HUVEC.{14066} The precise mechanisms of action by ARA-S and Abn-DBD in various vascular preparations appears to be different and requires further investigation.  

     

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    SKU:10005455 - 10 mg

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  • Arachidonoyl amides of both amino acids and neurotransmitters such as dopamine have been previously reported in the literature.{9213} N-Arachidonoyl-L-serine (ARA-S) is one such recently isolated endocannabinoid with an unusual activity profile. ARA-S does not bind to central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors or vanilloid receptor 1 (VR1). Like cannabidiol, ARA-S (5 mg/kg) antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model.{11984} However, similar to Abn-CBD, ARA-S relaxes isolated rat mesenteric arteries and abdominal aorta as well as increases phosphorylation of Akt and mitogen-activated protein kinase (MAPK) in HUVEC.{14066} The precise mechanisms of action by ARA-S and Abn-DBD in various vascular preparations appears to be different and requires further investigation.  

     

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    SKU:10005455 - 25 mg

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  • Arachidonoyl amides of both amino acids and neurotransmitters such as dopamine have been previously reported in the literature.{9213} N-Arachidonoyl-L-serine (ARA-S) is one such recently isolated endocannabinoid with an unusual activity profile. ARA-S does not bind to central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors or vanilloid receptor 1 (VR1). Like cannabidiol, ARA-S (5 mg/kg) antagonizes the hypotensive effects of a 10 mg/kg IV bolus of abnormal cannabidiol (Abn-CBD) in an anesthetized rat blood pressure model.{11984} However, similar to Abn-CBD, ARA-S relaxes isolated rat mesenteric arteries and abdominal aorta as well as increases phosphorylation of Akt and mitogen-activated protein kinase (MAPK) in HUVEC.{14066} The precise mechanisms of action by ARA-S and Abn-DBD in various vascular preparations appears to be different and requires further investigation.  

     

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    SKU:10005455 - 5 mg

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  • Several different arachidonoyl amino acids, including N-Arachidonoyl-γ-aminobutyric acid (NAGABA), have been isolated and characterized from bovine brain.The glycine congener (NAGly) was further characterized and found to suppress formalin-induced pain in rats. NAGABA was also found to suppress normal responses to pain, but has not been fully characterized to date.{9589}  

     

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    SKU:90067 - 10 mg

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  • Several different arachidonoyl amino acids, including N-Arachidonoyl-γ-aminobutyric acid (NAGABA), have been isolated and characterized from bovine brain.The glycine congener (NAGly) was further characterized and found to suppress formalin-induced pain in rats. NAGABA was also found to suppress normal responses to pain, but has not been fully characterized to date.{9589}  

     

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    SKU:90067 - 25 mg

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  • Several different arachidonoyl amino acids, including N-Arachidonoyl-γ-aminobutyric acid (NAGABA), have been isolated and characterized from bovine brain.The glycine congener (NAGly) was further characterized and found to suppress formalin-induced pain in rats. NAGABA was also found to suppress normal responses to pain, but has not been fully characterized to date.{9589}  

     

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    SKU:90067 - 5 mg

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  • 2-Arachidonoyl glycerol (2-AG) is an endogenous agonist of the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors.{7183,7182,9610} 2-AG is present at relatively high levels in the central nervous system and is the most abundant molecular species of monoacylglycerol found in rat brain.{7183,6819} Monoacylglycerol lipase (MGL) hydrolyzes 2-AG to arachidonic acid and glycerol, thereby terminating its biological actions.{11364} N-Arachidonyl maleimide (NAM) is a potent, irreversible inhibitor of monoacylglycerol lipase (MGL) or MGL-like activity in rat cerebellar membranes, exhibiting an IC50 value of 140 nM.{13255} Inhibition of MGL by the sulfhydryl-reactive maleimide group of NAM suggests a critical cysteine residue is present in the substrate-binding site of the enzyme.  

     

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    SKU:10007517 - 10 mg

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  • 2-Arachidonoyl glycerol (2-AG) is an endogenous agonist of the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors.{7183,7182,9610} 2-AG is present at relatively high levels in the central nervous system and is the most abundant molecular species of monoacylglycerol found in rat brain.{7183,6819} Monoacylglycerol lipase (MGL) hydrolyzes 2-AG to arachidonic acid and glycerol, thereby terminating its biological actions.{11364} N-Arachidonyl maleimide (NAM) is a potent, irreversible inhibitor of monoacylglycerol lipase (MGL) or MGL-like activity in rat cerebellar membranes, exhibiting an IC50 value of 140 nM.{13255} Inhibition of MGL by the sulfhydryl-reactive maleimide group of NAM suggests a critical cysteine residue is present in the substrate-binding site of the enzyme.  

     

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  • 2-Arachidonoyl glycerol (2-AG) is an endogenous agonist of the central cannabinoid (CB1) and peripheral cannabinoid (CB2) receptors.{7183,7182,9610} 2-AG is present at relatively high levels in the central nervous system and is the most abundant molecular species of monoacylglycerol found in rat brain.{7183,6819} Monoacylglycerol lipase (MGL) hydrolyzes 2-AG to arachidonic acid and glycerol, thereby terminating its biological actions.{11364} N-Arachidonyl maleimide (NAM) is a potent, irreversible inhibitor of monoacylglycerol lipase (MGL) or MGL-like activity in rat cerebellar membranes, exhibiting an IC50 value of 140 nM.{13255} Inhibition of MGL by the sulfhydryl-reactive maleimide group of NAM suggests a critical cysteine residue is present in the substrate-binding site of the enzyme.  

     

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  • N-Benzyl-4-piperidone (Item No. 21962) is an analytical reference standard that is structurally categorized as a piperidine. It is a starting material that is used in the synthesis of fentanyl (Item Nos. ISO60197 | 14719) and related compounds. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

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  • N-Benzyl-4-piperidone (Item No. 21962) is an analytical reference standard that is structurally categorized as a piperidine. It is a starting material that is used in the synthesis of fentanyl (Item Nos. ISO60197 | 14719) and related compounds. The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

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  • Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylacetamidine is a potent inhibitor of iNOS (IC50 = 0.20 μM), with over 1,000-fold selectivity compared to eNOS (IC50 = 350 µM).{17417}  

     

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  • Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylacetamidine is a potent inhibitor of iNOS (IC50 = 0.20 μM), with over 1,000-fold selectivity compared to eNOS (IC50 = 350 µM).{17417}  

     

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  • Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylacetamidine is a potent inhibitor of iNOS (IC50 = 0.20 μM), with over 1,000-fold selectivity compared to eNOS (IC50 = 350 µM).{17417}  

     

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  • Of the different types of nitric oxide synthases (NOS), the inducible (iNOS) form contributes to inflammation and immune response while the constitutively-expressed endothelial (eNOS) enzyme plays important roles in regulating vascular tone. N-Benzylacetamidine is a potent inhibitor of iNOS (IC50 = 0.20 μM), with over 1,000-fold selectivity compared to eNOS (IC50 = 350 µM).{17417}  

     

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  • N-Benzylpalmitamide is a long-chain fatty acid amide (macamide or macaene) isolated from the maca (L. meyenii) plant and is structurally related to cannabinoids.{28386} N-Benzylpalmitamide has been the most frequently isolated of the 19 macamides currently identified. While many macamides have been identified as potent inhibitors of fatty acid amide hydrolase (FAAH), N-benzylpalmitamide displays only moderate FAAH inhibitory activity (44% inhibition at 500 µM).{28386} Additionally, many members of this family demonstrate selective antiproliferative activity against diverse cancer cell lines.{28387}  

     

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    SKU:9002235 - 10 mg

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  • N-Benzylpalmitamide is a long-chain fatty acid amide (macamide or macaene) isolated from the maca (L. meyenii) plant and is structurally related to cannabinoids.{28386} N-Benzylpalmitamide has been the most frequently isolated of the 19 macamides currently identified. While many macamides have been identified as potent inhibitors of fatty acid amide hydrolase (FAAH), N-benzylpalmitamide displays only moderate FAAH inhibitory activity (44% inhibition at 500 µM).{28386} Additionally, many members of this family demonstrate selective antiproliferative activity against diverse cancer cell lines.{28387}  

     

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    SKU:9002235 - 100 mg

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  • N-Benzylpalmitamide is a long-chain fatty acid amide (macamide or macaene) isolated from the maca (L. meyenii) plant and is structurally related to cannabinoids.{28386} N-Benzylpalmitamide has been the most frequently isolated of the 19 macamides currently identified. While many macamides have been identified as potent inhibitors of fatty acid amide hydrolase (FAAH), N-benzylpalmitamide displays only moderate FAAH inhibitory activity (44% inhibition at 500 µM).{28386} Additionally, many members of this family demonstrate selective antiproliferative activity against diverse cancer cell lines.{28387}  

     

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    SKU:9002235 - 5 mg

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  • N-Benzylpalmitamide is a long-chain fatty acid amide (macamide or macaene) isolated from the maca (L. meyenii) plant and is structurally related to cannabinoids.{28386} N-Benzylpalmitamide has been the most frequently isolated of the 19 macamides currently identified. While many macamides have been identified as potent inhibitors of fatty acid amide hydrolase (FAAH), N-benzylpalmitamide displays only moderate FAAH inhibitory activity (44% inhibition at 500 µM).{28386} Additionally, many members of this family demonstrate selective antiproliferative activity against diverse cancer cell lines.{28387}  

     

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  • N-Boc Ketamine (Item No. 9003561) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.  

     

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  • N-Boc Ketamine (Item No. 9003561) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.  

     

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  • N-Boc Norketamine (Item No. 9003560) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.  

     

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  • N-Boc Norketamine (Item No. 9003560) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.  

     

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  • N-Boc-L-proline is a synthetic intermediate.{49607,49608} It has been used in the synthesis of enantioselective catalysts for aldol reactions and hepatitis C virus (HCV) NS5A inhibitors.  

     

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    SKU:30386 - 100 g

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  • N-Boc-L-proline is a synthetic intermediate.{49607,49608} It has been used in the synthesis of enantioselective catalysts for aldol reactions and hepatitis C virus (HCV) NS5A inhibitors.  

     

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    SKU:30386 - 25 g

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  • N-Boc-L-proline is a synthetic intermediate.{49607,49608} It has been used in the synthesis of enantioselective catalysts for aldol reactions and hepatitis C virus (HCV) NS5A inhibitors.  

     

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    SKU:30386 - 50 g

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  • N-butyl Amphetamine (hydrochloride) (Item No. 23547) is an analytical reference standard categorized as an amphetamine.{26035} This product is intended for research and forensic applications.  

     

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    SKU:23547 - 1 mg

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  • N-butyl Amphetamine (hydrochloride) (Item No. 23547) is an analytical reference standard categorized as an amphetamine.{26035} This product is intended for research and forensic applications.  

     

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  • N-butyl Pentylone (hydrochloride) (Item No. 26701) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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  • N-butyl Pentylone (hydrochloride) (Item No. 26701) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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  • N-Butyldeoxynojirimycin (NB-DNJ) is an iminosugar that inhibits ceramide-specific glucosyltransferase and β-glucosidase 2 (IC50s = 32 and 81 μM, respectively, for rat recombinant enzymes).{38202} The addition of NB-DNJ to growth medium for COS-7 cells expressing wild-type, S364R, N370S, V15M, or M123T glucocerebrosidase, an enzyme deficient in Spanish populations with the sphingolipid storage disorder Gaucher disease, leads to a 2.1-, 1.3-, 2.3-, 3.6,- or 9.9-fold increase in enzyme activity.{38203} NB-DNJ also inhibits HIV-1 and HIV-2 infection of peripheral blood mononuclear cells (PBMCs) with IC50 values of 282 and 211 μM, respectively.{38204} Formulations containing NB-DNJ have been used for the treatment of Gaucher disease and juvenile Sandhoff disease.{38205}  

     

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  • N-Butyldeoxynojirimycin (NB-DNJ) is an iminosugar that inhibits ceramide-specific glucosyltransferase and β-glucosidase 2 (IC50s = 32 and 81 μM, respectively, for rat recombinant enzymes).{38202} The addition of NB-DNJ to growth medium for COS-7 cells expressing wild-type, S364R, N370S, V15M, or M123T glucocerebrosidase, an enzyme deficient in Spanish populations with the sphingolipid storage disorder Gaucher disease, leads to a 2.1-, 1.3-, 2.3-, 3.6,- or 9.9-fold increase in enzyme activity.{38203} NB-DNJ also inhibits HIV-1 and HIV-2 infection of peripheral blood mononuclear cells (PBMCs) with IC50 values of 282 and 211 μM, respectively.{38204} Formulations containing NB-DNJ have been used for the treatment of Gaucher disease and juvenile Sandhoff disease.{38205}  

     

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    SKU:21065 -

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  • N-Butyldeoxynojirimycin (NB-DNJ) is an iminosugar that inhibits ceramide-specific glucosyltransferase and β-glucosidase 2 (IC50s = 32 and 81 μM, respectively, for rat recombinant enzymes).{38202} The addition of NB-DNJ to growth medium for COS-7 cells expressing wild-type, S364R, N370S, V15M, or M123T glucocerebrosidase, an enzyme deficient in Spanish populations with the sphingolipid storage disorder Gaucher disease, leads to a 2.1-, 1.3-, 2.3-, 3.6,- or 9.9-fold increase in enzyme activity.{38203} NB-DNJ also inhibits HIV-1 and HIV-2 infection of peripheral blood mononuclear cells (PBMCs) with IC50 values of 282 and 211 μM, respectively.{38204} Formulations containing NB-DNJ have been used for the treatment of Gaucher disease and juvenile Sandhoff disease.{38205}  

     

    Brand:
    Cayman
    SKU:21065 -

    Out of stock

  • N-Butyldeoxynojirimycin (NB-DNJ) is an iminosugar that inhibits ceramide-specific glucosyltransferase and β-glucosidase 2 (IC50s = 32 and 81 μM, respectively, for rat recombinant enzymes).{38202} The addition of NB-DNJ to growth medium for COS-7 cells expressing wild-type, S364R, N370S, V15M, or M123T glucocerebrosidase, an enzyme deficient in Spanish populations with the sphingolipid storage disorder Gaucher disease, leads to a 2.1-, 1.3-, 2.3-, 3.6,- or 9.9-fold increase in enzyme activity.{38203} NB-DNJ also inhibits HIV-1 and HIV-2 infection of peripheral blood mononuclear cells (PBMCs) with IC50 values of 282 and 211 μM, respectively.{38204} Formulations containing NB-DNJ have been used for the treatment of Gaucher disease and juvenile Sandhoff disease.{38205}  

     

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    Cayman
    SKU:21065 -

    Out of stock

  • N-Butylfluorescein is a fluorescent compound that displays excitation/emission maxima of 467/512 nm, respectively.{48518} It has been used in the synthesis of butyl fluorescein myo-inositol phosphate (butyl FLIP), a fluorogenic substrate of phosphatidylinositol-specific phospholipase C (PI-PLC).{48519}  

     

    Brand:
    Cayman
    SKU:20909 -

    Out of stock

  • N-Butylfluorescein is a fluorescent compound that displays excitation/emission maxima of 467/512 nm, respectively.{48518} It has been used in the synthesis of butyl fluorescein myo-inositol phosphate (butyl FLIP), a fluorogenic substrate of phosphatidylinositol-specific phospholipase C (PI-PLC).{48519}  

     

    Brand:
    Cayman
    SKU:20909 -

    Out of stock

  • N-Butylfluorescein is a fluorescent compound that displays excitation/emission maxima of 467/512 nm, respectively.{48518} It has been used in the synthesis of butyl fluorescein myo-inositol phosphate (butyl FLIP), a fluorogenic substrate of phosphatidylinositol-specific phospholipase C (PI-PLC).{48519}  

     

    Brand:
    Cayman
    SKU:20909 -

    Out of stock

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homocysteine thio-lactone is an analog of N-butyryl-L-homoserine lactone, the small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and cellular metabolism.{16309} N-butyryl-L-Homocysteine thio-lactone induces violacein expression in C. violaceum mutants usually not able to produce AHLs.{16309,16308}  

     

    Brand:
    Cayman
    SKU:10011204 - 10 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homocysteine thio-lactone is an analog of N-butyryl-L-homoserine lactone, the small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and cellular metabolism.{16309} N-butyryl-L-Homocysteine thio-lactone induces violacein expression in C. violaceum mutants usually not able to produce AHLs.{16309,16308}  

     

    Brand:
    Cayman
    SKU:10011204 - 25 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homocysteine thio-lactone is an analog of N-butyryl-L-homoserine lactone, the small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and cellular metabolism.{16309} N-butyryl-L-Homocysteine thio-lactone induces violacein expression in C. violaceum mutants usually not able to produce AHLs.{16309,16308}  

     

    Brand:
    Cayman
    SKU:10011204 - 5 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homocysteine thio-lactone is an analog of N-butyryl-L-homoserine lactone, the small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and cellular metabolism.{16309} N-butyryl-L-Homocysteine thio-lactone induces violacein expression in C. violaceum mutants usually not able to produce AHLs.{16309,16308}  

     

    Brand:
    Cayman
    SKU:10011204 - 50 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, controlling gene expression, and cellular metabolism.{13434} The diverse applications of this molecule include regulation of virulence in general, infection prevention, and formation of biofilms.{13433,14086,14087,14088,14089,14093}  

     

    Brand:
    Cayman
    SKU:10007898 - 10 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, controlling gene expression, and cellular metabolism.{13434} The diverse applications of this molecule include regulation of virulence in general, infection prevention, and formation of biofilms.{13433,14086,14087,14088,14089,14093}  

     

    Brand:
    Cayman
    SKU:10007898 - 25 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, controlling gene expression, and cellular metabolism.{13434} The diverse applications of this molecule include regulation of virulence in general, infection prevention, and formation of biofilms.{13433,14086,14087,14088,14089,14093}  

     

    Brand:
    Cayman
    SKU:10007898 - 5 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. Controlling bacterial infections by quenching their quorum sensing systems is a promising field of study. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-butyryl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, controlling gene expression, and cellular metabolism.{13434} The diverse applications of this molecule include regulation of virulence in general, infection prevention, and formation of biofilms.{13433,14086,14087,14088,14089,14093}  

     

    Brand:
    Cayman
    SKU:10007898 - 50 mg

    Available on backorder

  • N-Carbamyl-L-glutamic acid is an activator of carbamoyl phosphate synthetase 1 (CPS1), the first enzyme in the urea cycle.{38610} It is a structural analog of N-acetyl-glutamate, an endogenous CPS1 activator. N-Carbamyl-L-glutamic acid (500 mg/kg) reduces 2-ketoisocaproate-induced hyperammonemia in a mouse model of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.{38609} It inhibits cell proliferation of a variety of cancer cell lines with IC50 values ranging from 5 to 7.5 nM.{38608} It also inhibits tumor growth by 80 and 82% in orthotopic mouse models of pancreatic and triple-negative breast cancer, respectively, when administered at a dose of 120 mg/kg per day for 10 days. Formulations containing N-carbamyl-L-glutamic acid have been used in the treatment of primary N-acetyl-glutamate synthase deficiency.  

     

    Brand:
    Cayman
    SKU:23512 - 1 g

    Available on backorder

  • N-Carbamyl-L-glutamic acid is an activator of carbamoyl phosphate synthetase 1 (CPS1), the first enzyme in the urea cycle.{38610} It is a structural analog of N-acetyl-glutamate, an endogenous CPS1 activator. N-Carbamyl-L-glutamic acid (500 mg/kg) reduces 2-ketoisocaproate-induced hyperammonemia in a mouse model of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.{38609} It inhibits cell proliferation of a variety of cancer cell lines with IC50 values ranging from 5 to 7.5 nM.{38608} It also inhibits tumor growth by 80 and 82% in orthotopic mouse models of pancreatic and triple-negative breast cancer, respectively, when administered at a dose of 120 mg/kg per day for 10 days. Formulations containing N-carbamyl-L-glutamic acid have been used in the treatment of primary N-acetyl-glutamate synthase deficiency.  

     

    Brand:
    Cayman
    SKU:23512 - 10 g

    Available on backorder

  • N-Carbamyl-L-glutamic acid is an activator of carbamoyl phosphate synthetase 1 (CPS1), the first enzyme in the urea cycle.{38610} It is a structural analog of N-acetyl-glutamate, an endogenous CPS1 activator. N-Carbamyl-L-glutamic acid (500 mg/kg) reduces 2-ketoisocaproate-induced hyperammonemia in a mouse model of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.{38609} It inhibits cell proliferation of a variety of cancer cell lines with IC50 values ranging from 5 to 7.5 nM.{38608} It also inhibits tumor growth by 80 and 82% in orthotopic mouse models of pancreatic and triple-negative breast cancer, respectively, when administered at a dose of 120 mg/kg per day for 10 days. Formulations containing N-carbamyl-L-glutamic acid have been used in the treatment of primary N-acetyl-glutamate synthase deficiency.  

     

    Brand:
    Cayman
    SKU:23512 - 25 g

    Available on backorder

  • N-Carbamyl-L-glutamic acid is an activator of carbamoyl phosphate synthetase 1 (CPS1), the first enzyme in the urea cycle.{38610} It is a structural analog of N-acetyl-glutamate, an endogenous CPS1 activator. N-Carbamyl-L-glutamic acid (500 mg/kg) reduces 2-ketoisocaproate-induced hyperammonemia in a mouse model of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.{38609} It inhibits cell proliferation of a variety of cancer cell lines with IC50 values ranging from 5 to 7.5 nM.{38608} It also inhibits tumor growth by 80 and 82% in orthotopic mouse models of pancreatic and triple-negative breast cancer, respectively, when administered at a dose of 120 mg/kg per day for 10 days. Formulations containing N-carbamyl-L-glutamic acid have been used in the treatment of primary N-acetyl-glutamate synthase deficiency.  

     

    Brand:
    Cayman
    SKU:23512 - 5 g

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C16:1-Δ9-(L)-HSL is a long-chain AHL that functions as a quorum sensing signaling molecule in strains of S. meliloti.{15835,15834,15833,15828} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012673 - 10 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C16:1-Δ9-(L)-HSL is a long-chain AHL that functions as a quorum sensing signaling molecule in strains of S. meliloti.{15835,15834,15833,15828} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012673 - 25 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C16:1-Δ9-(L)-HSL is a long-chain AHL that functions as a quorum sensing signaling molecule in strains of S. meliloti.{15835,15834,15833,15828} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012673 - 5 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C16:1-Δ9-(L)-HSL is a long-chain AHL that functions as a quorum sensing signaling molecule in strains of S. meliloti.{15835,15834,15833,15828} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012673 - 50 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C18:1-Δ9 cis-(L)-HSL is a long-chain AHL that may have antimicrobial activity{15832} and thus, might be used to inhibit pathogenesis by regulating bacerial quorum sensing signaling.{15369}  

     

    Brand:
    Cayman
    SKU:10012674 - 10 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C18:1-Δ9 cis-(L)-HSL is a long-chain AHL that may have antimicrobial activity{15832} and thus, might be used to inhibit pathogenesis by regulating bacerial quorum sensing signaling.{15369}  

     

    Brand:
    Cayman
    SKU:10012674 - 25 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C18:1-Δ9 cis-(L)-HSL is a long-chain AHL that may have antimicrobial activity{15832} and thus, might be used to inhibit pathogenesis by regulating bacerial quorum sensing signaling.{15369}  

     

    Brand:
    Cayman
    SKU:10012674 - 5 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C18:1-Δ9 cis-(L)-HSL is a long-chain AHL that may have antimicrobial activity{15832} and thus, might be used to inhibit pathogenesis by regulating bacerial quorum sensing signaling.{15369}  

     

    Brand:
    Cayman
    SKU:10012674 - 50 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C14:1-Δ9-cis-(L)-HSL is a long-chain AHL that functions as a signaling molecule in the quorum sensing of A. vitis.{15831} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therpy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012672 - 10 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C14:1-Δ9-cis-(L)-HSL is a long-chain AHL that functions as a signaling molecule in the quorum sensing of A. vitis.{15831} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therpy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012672 - 25 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C14:1-Δ9-cis-(L)-HSL is a long-chain AHL that functions as a signaling molecule in the quorum sensing of A. vitis.{15831} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therpy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012672 - 5 mg

    Available on backorder

  • Quorum sensing is a regulatory process used by bacteria for controlling gene expression in response to increasing cell density.{15370} This regulatory process manifests itself with a variety of phenotypes including biofilm formation and virulence factor production.{13434} Coordinated gene expression is achieved by the production, release, and detection of small diffusible signal molecules called autoinducers. The N-acylated homoserine lactones (AHLs) comprise one such class of autoinducers, each of which generally consists of a fatty acid coupled with homoserine lactone (HSL). AHLs vary in acyl group length (C4-C18), in the substitution of C3 (hydrogen, hydroxyl, or oxo group) and in the presence or absence of one or more carbon-carbon double bonds in the fatty acid chain. These differences confer signal specificity through the affinity of transcriptional regulators of the LuxR family.{15398} C14:1-Δ9-cis-(L)-HSL is a long-chain AHL that functions as a signaling molecule in the quorum sensing of A. vitis.{15831} Regulating bacterial quorum sensing signaling can be used to inhibit pathogenesis and thus, represents a new approach to antimicrobial therpy in the treatment of infectious diseases.{15369}  

     

    Brand:
    Cayman
    SKU:10012672 - 50 mg

    Available on backorder

  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda has recently cloned another amidase, the acidic palmitoyl ethanolamidase (PEAase) that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonylpentadecylamine is a selective inhibitor of acidic PEAase, inhibiting the enzyme with an IC50 of 4.5 µM, while failing to inhibit FAAH even at 100 µM.{13342}  

     

    Brand:
    Cayman
    SKU:10007739 - 10 mg

    Available on backorder

  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda has recently cloned another amidase, the acidic palmitoyl ethanolamidase (PEAase) that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonylpentadecylamine is a selective inhibitor of acidic PEAase, inhibiting the enzyme with an IC50 of 4.5 µM, while failing to inhibit FAAH even at 100 µM.{13342}  

     

    Brand:
    Cayman
    SKU:10007739 - 100 mg

    Available on backorder

  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda has recently cloned another amidase, the acidic palmitoyl ethanolamidase (PEAase) that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonylpentadecylamine is a selective inhibitor of acidic PEAase, inhibiting the enzyme with an IC50 of 4.5 µM, while failing to inhibit FAAH even at 100 µM.{13342}  

     

    Brand:
    Cayman
    SKU:10007739 - 5 mg

    Available on backorder

  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda has recently cloned another amidase, the acidic palmitoyl ethanolamidase (PEAase) that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonylpentadecylamine is a selective inhibitor of acidic PEAase, inhibiting the enzyme with an IC50 of 4.5 µM, while failing to inhibit FAAH even at 100 µM.{13342}  

     

    Brand:
    Cayman
    SKU:10007739 - 50 mg

    Available on backorder

  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda, et al. has recently cloned another amidase, the acidic PEAase that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonyltetradecylamine is an analog of N-cyclohexanecarbonyl-pentadecylamine, a selective inhibitor of acidic PEAase with an IC50 value of 4.5 µM, that contains 1 less carbon in the alkyl chain.{13342} The biological activity of N-cyclohexanecarbonyltetradecylamine has not been documented.  

     

    Brand:
    Cayman
    SKU:10008317 - 10 mg

    Available on backorder

  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda, et al. has recently cloned another amidase, the acidic PEAase that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonyltetradecylamine is an analog of N-cyclohexanecarbonyl-pentadecylamine, a selective inhibitor of acidic PEAase with an IC50 value of 4.5 µM, that contains 1 less carbon in the alkyl chain.{13342} The biological activity of N-cyclohexanecarbonyltetradecylamine has not been documented.  

     

    Brand:
    Cayman
    SKU:10008317 - 100 mg

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  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda, et al. has recently cloned another amidase, the acidic PEAase that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonyltetradecylamine is an analog of N-cyclohexanecarbonyl-pentadecylamine, a selective inhibitor of acidic PEAase with an IC50 value of 4.5 µM, that contains 1 less carbon in the alkyl chain.{13342} The biological activity of N-cyclohexanecarbonyltetradecylamine has not been documented.  

     

    Brand:
    Cayman
    SKU:10008317 - 5 mg

    Available on backorder

  • Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda, et al. has recently cloned another amidase, the acidic PEAase that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonyltetradecylamine is an analog of N-cyclohexanecarbonyl-pentadecylamine, a selective inhibitor of acidic PEAase with an IC50 value of 4.5 µM, that contains 1 less carbon in the alkyl chain.{13342} The biological activity of N-cyclohexanecarbonyltetradecylamine has not been documented.  

     

    Brand:
    Cayman
    SKU:10008317 - 50 mg

    Available on backorder

  • N-Deacetylcolchicine is an inhibitor of tubulin polymerization (IC50 = 3 µM for bovine brain tubulin) and a derivative of the microtubule polymerization inhibitor colchicine (Item No. 9000760).{24891} It stimulates tubulin GTPase activity.{51178}  

     

    Brand:
    Cayman
    SKU:21697 -

    Out of stock

  • N-Deacetylcolchicine is an inhibitor of tubulin polymerization (IC50 = 3 µM for bovine brain tubulin) and a derivative of the microtubule polymerization inhibitor colchicine (Item No. 9000760).{24891} It stimulates tubulin GTPase activity.{51178}  

     

    Brand:
    Cayman
    SKU:21697 -

    Out of stock

  • N-Deacetylcolchicine is an inhibitor of tubulin polymerization (IC50 = 3 µM for bovine brain tubulin) and a derivative of the microtubule polymerization inhibitor colchicine (Item No. 9000760).{24891} It stimulates tubulin GTPase activity.{51178}  

     

    Brand:
    Cayman
    SKU:21697 -

    Out of stock

  • N-Deacetylcolchicine is an inhibitor of tubulin polymerization (IC50 = 3 µM for bovine brain tubulin) and a derivative of the microtubule polymerization inhibitor colchicine (Item No. 9000760).{24891} It stimulates tubulin GTPase activity.{51178}  

     

    Brand:
    Cayman
    SKU:21697 -

    Out of stock

  • N-Decanoyl p-nitroaniline (DepNA) is one of several nitroaniline fatty acid amides which can be used to measure fatty acid amide hydrolase (FAAH) activity.{8928} FAAH is a relatively unselective enzyme in that it accepts a variety of amide head groups other than the ethanolamine of its endogenous substrate anandamide (AEA). It also will hydrolyze fatty acid amides with fewer carbons and fewer double bonds than arachidonate. Exposure of DepNA to FAAH activity results in the release of the yellow colorimetric dye p-nitroaniline (ε = 13,500 at 410 nm). This allows the fast and convenient measurement of FAAH activity using a 96 well plate spectrophotometer.  

     

    Brand:
    Cayman
    SKU:10005851 - 10 mg

    Available on backorder

  • N-Decanoyl p-nitroaniline (DepNA) is one of several nitroaniline fatty acid amides which can be used to measure fatty acid amide hydrolase (FAAH) activity.{8928} FAAH is a relatively unselective enzyme in that it accepts a variety of amide head groups other than the ethanolamine of its endogenous substrate anandamide (AEA). It also will hydrolyze fatty acid amides with fewer carbons and fewer double bonds than arachidonate. Exposure of DepNA to FAAH activity results in the release of the yellow colorimetric dye p-nitroaniline (ε = 13,500 at 410 nm). This allows the fast and convenient measurement of FAAH activity using a 96 well plate spectrophotometer.  

     

    Brand:
    Cayman
    SKU:10005851 - 25 mg

    Available on backorder

  • N-Decanoyl p-nitroaniline (DepNA) is one of several nitroaniline fatty acid amides which can be used to measure fatty acid amide hydrolase (FAAH) activity.{8928} FAAH is a relatively unselective enzyme in that it accepts a variety of amide head groups other than the ethanolamine of its endogenous substrate anandamide (AEA). It also will hydrolyze fatty acid amides with fewer carbons and fewer double bonds than arachidonate. Exposure of DepNA to FAAH activity results in the release of the yellow colorimetric dye p-nitroaniline (ε = 13,500 at 410 nm). This allows the fast and convenient measurement of FAAH activity using a 96 well plate spectrophotometer.  

     

    Brand:
    Cayman
    SKU:10005851 - 5 mg

    Available on backorder

  • N-Decanoyl p-nitroaniline (DepNA) is one of several nitroaniline fatty acid amides which can be used to measure fatty acid amide hydrolase (FAAH) activity.{8928} FAAH is a relatively unselective enzyme in that it accepts a variety of amide head groups other than the ethanolamine of its endogenous substrate anandamide (AEA). It also will hydrolyze fatty acid amides with fewer carbons and fewer double bonds than arachidonate. Exposure of DepNA to FAAH activity results in the release of the yellow colorimetric dye p-nitroaniline (ε = 13,500 at 410 nm). This allows the fast and convenient measurement of FAAH activity using a 96 well plate spectrophotometer.  

     

    Brand:
    Cayman
    SKU:10005851 - 50 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. A promising field of study involves controlling bacterial infections by quenching their quorum sensing systems. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-decanoyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism.{16304} The applications of this molecule include regulation of virulence and exoproteases.{15399}  

     

    Brand:
    Cayman
    SKU:10011201 - 10 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. A promising field of study involves controlling bacterial infections by quenching their quorum sensing systems. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-decanoyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism.{16304} The applications of this molecule include regulation of virulence and exoproteases.{15399}  

     

    Brand:
    Cayman
    SKU:10011201 - 25 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. A promising field of study involves controlling bacterial infections by quenching their quorum sensing systems. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-decanoyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism.{16304} The applications of this molecule include regulation of virulence and exoproteases.{15399}  

     

    Brand:
    Cayman
    SKU:10011201 - 5 mg

    Available on backorder

  • Quorum sensing is a regulatory system used by bacteria for controlling gene expression in response to increasing cell density. A promising field of study involves controlling bacterial infections by quenching their quorum sensing systems. The expression of specific target genes, such as transcriptional regulators belonging to the LuxIR family of proteins, is coordinated by synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-decanoyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism.{16304} The applications of this molecule include regulation of virulence and exoproteases.{15399}  

     

    Brand:
    Cayman
    SKU:10011201 - 50 mg

    Available on backorder

  • n-Decyl-β-D-maltoside is a nonionic surfactant that is commonly used to solubilize and stabilize membrane proteins.{46041,46042} It has a critical micelle concentration (CMC) value of 1.8 mM and has been used in the expression of functional recombinant GPCRs.  

     

    Brand:
    Cayman
    SKU:25704 - 1 g

    Available on backorder

  • n-Decyl-β-D-maltoside is a nonionic surfactant that is commonly used to solubilize and stabilize membrane proteins.{46041,46042} It has a critical micelle concentration (CMC) value of 1.8 mM and has been used in the expression of functional recombinant GPCRs.  

     

    Brand:
    Cayman
    SKU:25704 - 5 g

    Available on backorder

  • N-Demethylerythromycin A is a metabolite of erythromycin (Item No. 16486).{43941} It is also a fungal metabolite that has been found in S. erythreus and a potential impurity in commercial preparations of erythromycin.{35178}  

     

    Brand:
    Cayman
    SKU:27988 - 1 mg

    Available on backorder

  • N-Demethylerythromycin A is a metabolite of erythromycin (Item No. 16486).{43941} It is also a fungal metabolite that has been found in S. erythreus and a potential impurity in commercial preparations of erythromycin.{35178}  

     

    Brand:
    Cayman
    SKU:27988 - 10 mg

    Available on backorder

  • N-Demethylerythromycin A is a metabolite of erythromycin (Item No. 16486).{43941} It is also a fungal metabolite that has been found in S. erythreus and a potential impurity in commercial preparations of erythromycin.{35178}  

     

    Brand:
    Cayman
    SKU:27988 - 5 mg

    Available on backorder

  • N-Demethylerythromycin A is a metabolite of erythromycin (Item No. 16486).{43941} It is also a fungal metabolite that has been found in S. erythreus and a potential impurity in commercial preparations of erythromycin.{35178}  

     

    Brand:
    Cayman
    SKU:27988 - 500 µg

    Available on backorder

  • N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine (Item No. 15954), produced by the action of cytochrome P450 isoform 2C8.{26894} N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.{26895}  

     

    Brand:
    Cayman
    SKU:20822 -

    Out of stock

  • N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine (Item No. 15954), produced by the action of cytochrome P450 isoform 2C8.{26894} N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.{26895}  

     

    Brand:
    Cayman
    SKU:20822 -

    Out of stock

  • N-desethyl Amodiaquine is a primary metabolite of the antimalarial compound aminodiaquine (Item No. 15954), produced by the action of cytochrome P450 isoform 2C8.{26894} N-desethyl Amodiaquine is highly active against P. falciparum and can synergize with amodiaquine.{26895}  

     

    Brand:
    Cayman
    SKU:20822 -

    Out of stock

  • N-desethyl Sunitinib is an active metabolite of sunitinib (Item No. 13159), a small molecule, multi-targeted receptor tyrosine kinase inhibitor.{17043,40284} N-desethyl Sunitinib is formed when sunitinib undergoes N-de-ethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40284} N-desethyl Sunitinib is pharmacologically active having similar inhibitory activity to sunitinib.  

     

    Brand:
    Cayman
    SKU:22292 -

    Out of stock

  • N-desethyl Sunitinib is an active metabolite of sunitinib (Item No. 13159), a small molecule, multi-targeted receptor tyrosine kinase inhibitor.{17043,40284} N-desethyl Sunitinib is formed when sunitinib undergoes N-de-ethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40284} N-desethyl Sunitinib is pharmacologically active having similar inhibitory activity to sunitinib.  

     

    Brand:
    Cayman
    SKU:22292 -

    Out of stock

  • N-desethyl Sunitinib is an active metabolite of sunitinib (Item No. 13159), a small molecule, multi-targeted receptor tyrosine kinase inhibitor.{17043,40284} N-desethyl Sunitinib is formed when sunitinib undergoes N-de-ethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40284} N-desethyl Sunitinib is pharmacologically active having similar inhibitory activity to sunitinib.  

     

    Brand:
    Cayman
    SKU:22292 -

    Out of stock

  • N-desethyl Sunitinib is an active metabolite of sunitinib (Item No. 13159), a small molecule, multi-targeted receptor tyrosine kinase inhibitor.{17043,40284} N-desethyl Sunitinib is formed when sunitinib undergoes N-de-ethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40284} N-desethyl Sunitinib is pharmacologically active having similar inhibitory activity to sunitinib.  

     

    Brand:
    Cayman
    SKU:22292 -

    Out of stock

  • N-Desethyl vardenafil is a metabolite of vardenafil (Item No. 14930), a phosphodiesterase 5 inhibitor, that is formed by the action of cytochrome P450 (CYP)3A4 and CYP3A5.{31630}  

     

    Brand:
    Cayman
    SKU:9001800 - 1 mg

    Available on backorder

  • N-Desethyl vardenafil is a metabolite of vardenafil (Item No. 14930), a phosphodiesterase 5 inhibitor, that is formed by the action of cytochrome P450 (CYP)3A4 and CYP3A5.{31630}  

     

    Brand:
    Cayman
    SKU:9001800 - 5 mg

    Available on backorder

  • N-Desethyl vardenafil is a metabolite of vardenafil (Item No. 14930), a phosphodiesterase 5 inhibitor, that is formed by the action of cytochrome P450 (CYP)3A4 and CYP3A5.{31630}  

     

    Brand:
    Cayman
    SKU:9001800 - 500 µg

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  • Amiodarone (Item No. 15213) is a class III antiarrhythmic agent, in that it prolongs both cardiac action potential and refractoriness by blocking potassium currents.{22478} It inhibits the voltage-gated potassium channel hERG, also known as KCNH2, with an IC50 value of 1 µM.{24593} In humans, cytochrome P450 3A is involved in the metabolism of amiodarone.{29074} N-Desethylamiodarone is the major, active metabolite of amiodarone. This compound has been used as an analytical reference standard for quantifying amiodarone in plasma samples.{29075}  

     

    Brand:
    Cayman
    SKU:9000537 - 10 mg

    Available on backorder

  • Amiodarone (Item No. 15213) is a class III antiarrhythmic agent, in that it prolongs both cardiac action potential and refractoriness by blocking potassium currents.{22478} It inhibits the voltage-gated potassium channel hERG, also known as KCNH2, with an IC50 value of 1 µM.{24593} In humans, cytochrome P450 3A is involved in the metabolism of amiodarone.{29074} N-Desethylamiodarone is the major, active metabolite of amiodarone. This compound has been used as an analytical reference standard for quantifying amiodarone in plasma samples.{29075}  

     

    Brand:
    Cayman
    SKU:9000537 - 100 mg

    Available on backorder

  • Amiodarone (Item No. 15213) is a class III antiarrhythmic agent, in that it prolongs both cardiac action potential and refractoriness by blocking potassium currents.{22478} It inhibits the voltage-gated potassium channel hERG, also known as KCNH2, with an IC50 value of 1 µM.{24593} In humans, cytochrome P450 3A is involved in the metabolism of amiodarone.{29074} N-Desethylamiodarone is the major, active metabolite of amiodarone. This compound has been used as an analytical reference standard for quantifying amiodarone in plasma samples.{29075}  

     

    Brand:
    Cayman
    SKU:9000537 - 250 mg

    Available on backorder

  • Amiodarone (Item No. 15213) is a class III antiarrhythmic agent, in that it prolongs both cardiac action potential and refractoriness by blocking potassium currents.{22478} It inhibits the voltage-gated potassium channel hERG, also known as KCNH2, with an IC50 value of 1 µM.{24593} In humans, cytochrome P450 3A is involved in the metabolism of amiodarone.{29074} N-Desethylamiodarone is the major, active metabolite of amiodarone. This compound has been used as an analytical reference standard for quantifying amiodarone in plasma samples.{29075}  

     

    Brand:
    Cayman
    SKU:9000537 - 50 mg

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  • N-desmethyl Bendamustine is an active metabolite of the DNA alkylating agent bendamustine (Item No. 23693).{49043} N-desmethyl Bendamustine is formed through demethylation of the benzimidazole ring in bendamustine by the cytochrome P450 (CYP) isoform CYP1A2. It inhibits proliferation of non-cancerous peripheral blood leukocytes (PBLs; IC50 = 45 µM) and SU-DHL-1, SU-DHL-9, and Daudi lymphoma cells (IC50s = 270, 170, and 120 µM, respectively).  

     

    Brand:
    Cayman
    SKU:27171 - 1 mg

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  • N-desmethyl Bendamustine is an active metabolite of the DNA alkylating agent bendamustine (Item No. 23693).{49043} N-desmethyl Bendamustine is formed through demethylation of the benzimidazole ring in bendamustine by the cytochrome P450 (CYP) isoform CYP1A2. It inhibits proliferation of non-cancerous peripheral blood leukocytes (PBLs; IC50 = 45 µM) and SU-DHL-1, SU-DHL-9, and Daudi lymphoma cells (IC50s = 270, 170, and 120 µM, respectively).  

     

    Brand:
    Cayman
    SKU:27171 - 500 µg

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  • N-desmethyl Imatinib is a major active metabolite of imatinib (Item No. 13139), an anticancer agent that selectively targets tyrosine kinases, including Bcr-ABL, platelet-derived growth factor receptor (PDGFR), and KIT.{17064,17065} N-desmethyl Imatinib is formed when imatinib undergoes demethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40229} N-desmethyl Imatinib has the same in vitro potency at Bcr-ABL kinase as imatinib (IC50 = 38 nM for both) but is only present in plasma at 10-15% of the levels of imatinib, indicating the majority of the anticancer activity can be attributed to the parent compound.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • N-desmethyl Imatinib is a major active metabolite of imatinib (Item No. 13139), an anticancer agent that selectively targets tyrosine kinases, including Bcr-ABL, platelet-derived growth factor receptor (PDGFR), and KIT.{17064,17065} N-desmethyl Imatinib is formed when imatinib undergoes demethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40229} N-desmethyl Imatinib has the same in vitro potency at Bcr-ABL kinase as imatinib (IC50 = 38 nM for both) but is only present in plasma at 10-15% of the levels of imatinib, indicating the majority of the anticancer activity can be attributed to the parent compound.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • N-desmethyl Imatinib is a major active metabolite of imatinib (Item No. 13139), an anticancer agent that selectively targets tyrosine kinases, including Bcr-ABL, platelet-derived growth factor receptor (PDGFR), and KIT.{17064,17065} N-desmethyl Imatinib is formed when imatinib undergoes demethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40229} N-desmethyl Imatinib has the same in vitro potency at Bcr-ABL kinase as imatinib (IC50 = 38 nM for both) but is only present in plasma at 10-15% of the levels of imatinib, indicating the majority of the anticancer activity can be attributed to the parent compound.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • N-desmethyl Imatinib is a major active metabolite of imatinib (Item No. 13139), an anticancer agent that selectively targets tyrosine kinases, including Bcr-ABL, platelet-derived growth factor receptor (PDGFR), and KIT.{17064,17065} N-desmethyl Imatinib is formed when imatinib undergoes demethylation by the cytochrome P450 (CYP) isomer CYP3A4.{40229} N-desmethyl Imatinib has the same in vitro potency at Bcr-ABL kinase as imatinib (IC50 = 38 nM for both) but is only present in plasma at 10-15% of the levels of imatinib, indicating the majority of the anticancer activity can be attributed to the parent compound.  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • N-desmethyl Ivabradine is an active metabolite of ivabradine (Item No. 15868).{42971} Ivabradine is metabolized by the cytochrome P450 (CYP) isoform CYP3A4.  

     

    Brand:
    Cayman
    SKU:27808 - 1 mg

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  • N-desmethyl Ivabradine is an active metabolite of ivabradine (Item No. 15868).{42971} Ivabradine is metabolized by the cytochrome P450 (CYP) isoform CYP3A4.  

     

    Brand:
    Cayman
    SKU:27808 - 10 mg

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  • N-desmethyl Ivabradine is an active metabolite of ivabradine (Item No. 15868).{42971} Ivabradine is metabolized by the cytochrome P450 (CYP) isoform CYP3A4.  

     

    Brand:
    Cayman
    SKU:27808 - 5 mg

    Available on backorder

  • N-desmethyl Levofloxacin is an active metabolite of the fluoroquinolone antibiotic levofloxacin (Item No. 20382).{45220} It is active against S. aureus, S. epidermidis, B. subtilis, E. coli, P. aeruginosa, and K. pneumoniae (MICs = 4, 1, 1, 0.012, >4, and 0.25 μg/ml, respectively).  

     

    Brand:
    Cayman
    SKU:27178 - 10 mg

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  • N-desmethyl Levofloxacin is an active metabolite of the fluoroquinolone antibiotic levofloxacin (Item No. 20382).{45220} It is active against S. aureus, S. epidermidis, B. subtilis, E. coli, P. aeruginosa, and K. pneumoniae (MICs = 4, 1, 1, 0.012, >4, and 0.25 μg/ml, respectively).  

     

    Brand:
    Cayman
    SKU:27178 - 25 mg

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  • N-desmethyl Levofloxacin is an active metabolite of the fluoroquinolone antibiotic levofloxacin (Item No. 20382).{45220} It is active against S. aureus, S. epidermidis, B. subtilis, E. coli, P. aeruginosa, and K. pneumoniae (MICs = 4, 1, 1, 0.012, >4, and 0.25 μg/ml, respectively).  

     

    Brand:
    Cayman
    SKU:27178 - 5 mg

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  • N-desmethyl Rosiglitazone is a major metabolite of rosiglitazone (Item Nos. 71740 | 71742 | 11884), a potent and selective PPARγ ligand present in formulations that have been used to treat type 2 diabetes.{8461,41078} Rosiglitazone is metabolized by the cytochrome P450 (CYP) isoform CYP2C8 to form N-desmethyl rosiglitazone.  

     

    Brand:
    Cayman
    SKU:22103 -

    Out of stock

  • N-desmethyl Rosiglitazone is a major metabolite of rosiglitazone (Item Nos. 71740 | 71742 | 11884), a potent and selective PPARγ ligand present in formulations that have been used to treat type 2 diabetes.{8461,41078} Rosiglitazone is metabolized by the cytochrome P450 (CYP) isoform CYP2C8 to form N-desmethyl rosiglitazone.  

     

    Brand:
    Cayman
    SKU:22103 -

    Out of stock

  • N-desmethyl Rosiglitazone is a major metabolite of rosiglitazone (Item Nos. 71740 | 71742 | 11884), a potent and selective PPARγ ligand present in formulations that have been used to treat type 2 diabetes.{8461,41078} Rosiglitazone is metabolized by the cytochrome P450 (CYP) isoform CYP2C8 to form N-desmethyl rosiglitazone.  

     

    Brand:
    Cayman
    SKU:22103 -

    Out of stock

  • N-Desmethyl sildenafil is a major metabolite of sildenafil (Item Nos. 10008671 | 14008).{29612,29611,42395} N-Desmethyl sildenafil is formed via oxidative metabolism of sildenafil by the cytochrome (CYP) P450 isoforms CYP3A4, CYP3A5, and CYP3A7.{42395}  

     

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    Cayman
    SKU:-

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  • N-Desmethyl sildenafil is a major metabolite of sildenafil (Item Nos. 10008671 | 14008).{29612,29611,42395} N-Desmethyl sildenafil is formed via oxidative metabolism of sildenafil by the cytochrome (CYP) P450 isoforms CYP3A4, CYP3A5, and CYP3A7.{42395}  

     

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    Cayman
    SKU:-

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  • N-Desmethyl sildenafil is a major metabolite of sildenafil (Item Nos. 10008671 | 14008).{29612,29611,42395} N-Desmethyl sildenafil is formed via oxidative metabolism of sildenafil by the cytochrome (CYP) P450 isoforms CYP3A4, CYP3A5, and CYP3A7.{42395}  

     

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    Cayman
    SKU:-

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  • N-Desmethyl sildenafil is a major metabolite of sildenafil (Item Nos. 10008671 | 14008).{29612,29611,42395} N-Desmethyl sildenafil is formed via oxidative metabolism of sildenafil by the cytochrome (CYP) P450 isoforms CYP3A4, CYP3A5, and CYP3A7.{42395}  

     

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    Cayman
    SKU:-

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  • N-desmethyl Zolmitriptan (DZT) is an active metabolite of the serotonin (5-HT) receptor subtype 5-HT1B and 5-HT1D agonist zolmitriptan (Item No. 15871).{43950} DZT is an agonist of 5-HT1B receptors that induces contraction of isolated human cerebral arteries (EC50 = 100 nM).{43951}  

     

    Brand:
    Cayman
    SKU:28058 - 5 mg

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  • Loperamide (Item No. 14875) is an opiate which potently and selectively activates μ opioid receptors (Ki = 0.16 nM) exclusively in the periphery.{23761,23758} N-Desmethyl-loperamide (dLop) is a major metabolite of loperamide.{26350,26349} Like loperamide, dLop is a substrate of the ATP-dependent efflux transporter, P-glycoprotein.{26349,26352} As a result, both the parent compound and the metabolite display restricted passage through the blood-brain barrier.{26352,26348} dLop in biological samples can be analyzed by a variety of methods.{26350,26353}  

     

    Brand:
    Cayman
    SKU:-
  • Loperamide (Item No. 14875) is an opiate which potently and selectively activates μ opioid receptors (Ki = 0.16 nM) exclusively in the periphery.{23761,23758} N-Desmethyl-loperamide (dLop) is a major metabolite of loperamide.{26350,26349} Like loperamide, dLop is a substrate of the ATP-dependent efflux transporter, P-glycoprotein.{26349,26352} As a result, both the parent compound and the metabolite display restricted passage through the blood-brain barrier.{26352,26348} dLop in biological samples can be analyzed by a variety of methods.{26350,26353}  

     

    Brand:
    Cayman
    SKU:-
  • Loperamide (Item No. 14875) is an opiate which potently and selectively activates μ opioid receptors (Ki = 0.16 nM) exclusively in the periphery.{23761,23758} N-Desmethyl-loperamide (dLop) is a major metabolite of loperamide.{26350,26349} Like loperamide, dLop is a substrate of the ATP-dependent efflux transporter, P-glycoprotein.{26349,26352} As a result, both the parent compound and the metabolite display restricted passage through the blood-brain barrier.{26352,26348} dLop in biological samples can be analyzed by a variety of methods.{26350,26353}  

     

    Brand:
    Cayman
    SKU:-
  • N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine (Item Nos. 12059 | 25779).{25512} It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.{47099,47100} N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.{47100,25512,47101} N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibition of the acoustic startle response in mice.{47102}  

     

    Brand:
    Cayman
    SKU:26153 - 10 mg

    Available on backorder

  • N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine (Item Nos. 12059 | 25779).{25512} It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.{47099,47100} N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.{47100,25512,47101} N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibition of the acoustic startle response in mice.{47102}  

     

    Brand:
    Cayman
    SKU:26153 - 100 mg

    Available on backorder

  • N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine (Item Nos. 12059 | 25779).{25512} It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.{47099,47100} N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.{47100,25512,47101} N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibition of the acoustic startle response in mice.{47102}  

     

    Brand:
    Cayman
    SKU:26153 - 5 mg

    Available on backorder

  • N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine (Item Nos. 12059 | 25779).{25512} It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.{47099,47100} N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.{47100,25512,47101} N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibition of the acoustic startle response in mice.{47102}  

     

    Brand:
    Cayman
    SKU:26153 - 50 mg

    Available on backorder

  • N-Desmethylclozapine-d8 is intended for use as an internal standard for the quantification of N-desmethylclozapine by GC- or LC-MS. N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine (Item Nos. 12059 | 25779).{25512} It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.{47099,47100} N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.{47100,25512,47101} N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibiton of the acoustic startle response in mice.{47102}  

     

    Brand:
    Cayman
    SKU:26027 - 1 mg

    Available on backorder

  • N-Desmethylclozapine-d8 is intended for use as an internal standard for the quantification of N-desmethylclozapine by GC- or LC-MS. N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine (Item Nos. 12059 | 25779).{25512} It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.{47099,47100} N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.{47100,25512,47101} N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibiton of the acoustic startle response in mice.{47102}  

     

    Brand:
    Cayman
    SKU:26027 - 500 µg

    Available on backorder

  • N-Docosahexaenoyl dopamine (DHA-DA) is an amine conjugate of the neurotransmitter dopamine and the polyunsaturated fatty acid docosahexaenoic acid (DHA; Item No. 90310). DHA-DA is actively transported into the brain following intraperitoneal injections in mice, resulting in reduced general locomotor activity of 35-40% at a dose of 5 mg/kg.{13595} It is theorized that the DHA portion of the molecule serves as a carrier for DA through the blood-brain barrier via a DHA-mediated transport system.{13595} DHA-DA exhibits immune-modulating, anti-inflammatory activity in the range of 0.1-2.5 µM, suppressing the production of nitric oxide, IL-6, CCL20, MCP-1, and PGE2 (Item No. 14010) in LPS-stimulated macrophages and microglial cells without affecting NF-κB activity.{32905}  

     

    Brand:
    Cayman
    SKU:9001394 - 1 mg

    Available on backorder

  • N-Docosahexaenoyl dopamine (DHA-DA) is an amine conjugate of the neurotransmitter dopamine and the polyunsaturated fatty acid docosahexaenoic acid (DHA; Item No. 90310). DHA-DA is actively transported into the brain following intraperitoneal injections in mice, resulting in reduced general locomotor activity of 35-40% at a dose of 5 mg/kg.{13595} It is theorized that the DHA portion of the molecule serves as a carrier for DA through the blood-brain barrier via a DHA-mediated transport system.{13595} DHA-DA exhibits immune-modulating, anti-inflammatory activity in the range of 0.1-2.5 µM, suppressing the production of nitric oxide, IL-6, CCL20, MCP-1, and PGE2 (Item No. 14010) in LPS-stimulated macrophages and microglial cells without affecting NF-κB activity.{32905}  

     

    Brand:
    Cayman
    SKU:9001394 - 10 mg

    Available on backorder

  • N-Docosahexaenoyl dopamine (DHA-DA) is an amine conjugate of the neurotransmitter dopamine and the polyunsaturated fatty acid docosahexaenoic acid (DHA; Item No. 90310). DHA-DA is actively transported into the brain following intraperitoneal injections in mice, resulting in reduced general locomotor activity of 35-40% at a dose of 5 mg/kg.{13595} It is theorized that the DHA portion of the molecule serves as a carrier for DA through the blood-brain barrier via a DHA-mediated transport system.{13595} DHA-DA exhibits immune-modulating, anti-inflammatory activity in the range of 0.1-2.5 µM, suppressing the production of nitric oxide, IL-6, CCL20, MCP-1, and PGE2 (Item No. 14010) in LPS-stimulated macrophages and microglial cells without affecting NF-κB activity.{32905}  

     

    Brand:
    Cayman
    SKU:9001394 - 25 mg

    Available on backorder

  • N-Docosahexaenoyl dopamine (DHA-DA) is an amine conjugate of the neurotransmitter dopamine and the polyunsaturated fatty acid docosahexaenoic acid (DHA; Item No. 90310). DHA-DA is actively transported into the brain following intraperitoneal injections in mice, resulting in reduced general locomotor activity of 35-40% at a dose of 5 mg/kg.{13595} It is theorized that the DHA portion of the molecule serves as a carrier for DA through the blood-brain barrier via a DHA-mediated transport system.{13595} DHA-DA exhibits immune-modulating, anti-inflammatory activity in the range of 0.1-2.5 µM, suppressing the production of nitric oxide, IL-6, CCL20, MCP-1, and PGE2 (Item No. 14010) in LPS-stimulated macrophages and microglial cells without affecting NF-κB activity.{32905}  

     

    Brand:
    Cayman
    SKU:9001394 - 5 mg

    Available on backorder