Chemicals

Showing 28501–28650 of 41137 results

  • N-Oleoyl leucine is an N-acyl amide generated by PM20D1 that uncouples mitochondrial respiration independent of uncoupling protein 1 (UCP1) in vitro.{31656} N-Oleoyl leucine (25 mg/kg, i.p.) decreases body weight and food intake, preferentially decreasing fat mass in a diet-induced obesity mouse model. It improves glucose homeostasis in a fasting glucose tolerance test and increases VO2 while slightly decreasing overall locomotor activity.  

     

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    SKU:20064 -

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  • N-Oleoyl leucine is an N-acyl amide generated by PM20D1 that uncouples mitochondrial respiration independent of uncoupling protein 1 (UCP1) in vitro.{31656} N-Oleoyl leucine (25 mg/kg, i.p.) decreases body weight and food intake, preferentially decreasing fat mass in a diet-induced obesity mouse model. It improves glucose homeostasis in a fasting glucose tolerance test and increases VO2 while slightly decreasing overall locomotor activity.  

     

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    Cayman
    SKU:20064 -

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  • N-Oleoyl leucine is an N-acyl amide generated by PM20D1 that uncouples mitochondrial respiration independent of uncoupling protein 1 (UCP1) in vitro.{31656} N-Oleoyl leucine (25 mg/kg, i.p.) decreases body weight and food intake, preferentially decreasing fat mass in a diet-induced obesity mouse model. It improves glucose homeostasis in a fasting glucose tolerance test and increases VO2 while slightly decreasing overall locomotor activity.  

     

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    Cayman
    SKU:20064 -

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  • N-Oleoyl proline is an N-acyl amine that has been detected in bovine brain extracts and D. melanogaster larvae using mass spectrometry.{33754,33755} In a preclinical model of pain, mice lacking fatty acid amide hydrolase (FAAH KO) had decreased N-oleoyl proline levels in lumbar spinal cord after capsaicin administration (1 µg/10 µl).{33751} N-Oleoyl proline also has surfactant properties (critical micelle concentration = 4.8 µM).{33753}  

     

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    Cayman
    SKU:20369 -

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  • N-Oleoyl proline is an N-acyl amine that has been detected in bovine brain extracts and D. melanogaster larvae using mass spectrometry.{33754,33755} In a preclinical model of pain, mice lacking fatty acid amide hydrolase (FAAH KO) had decreased N-oleoyl proline levels in lumbar spinal cord after capsaicin administration (1 µg/10 µl).{33751} N-Oleoyl proline also has surfactant properties (critical micelle concentration = 4.8 µM).{33753}  

     

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    Cayman
    SKU:20369 -

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  • N-Oleoyl proline is an N-acyl amine that has been detected in bovine brain extracts and D. melanogaster larvae using mass spectrometry.{33754,33755} In a preclinical model of pain, mice lacking fatty acid amide hydrolase (FAAH KO) had decreased N-oleoyl proline levels in lumbar spinal cord after capsaicin administration (1 µg/10 µl).{33751} N-Oleoyl proline also has surfactant properties (critical micelle concentration = 4.8 µM).{33753}  

     

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    Cayman
    SKU:20369 -

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  • N-Oleoyl proline is an N-acyl amine that has been detected in bovine brain extracts and D. melanogaster larvae using mass spectrometry.{33754,33755} In a preclinical model of pain, mice lacking fatty acid amide hydrolase (FAAH KO) had decreased N-oleoyl proline levels in lumbar spinal cord after capsaicin administration (1 µg/10 µl).{33751} N-Oleoyl proline also has surfactant properties (critical micelle concentration = 4.8 µM).{33753}  

     

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    Cayman
    SKU:20369 -

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine and N-arachidonoyl serine, have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomics analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, were discovered.{12336} This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels.{16245} N-Oleoyl taurine is an amino-acyl endocannabinoid isolated from rat brain that may activate TRPV1 and TRPV4.{16245}  

     

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    SKU:10005609 - 1 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine and N-arachidonoyl serine, have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomics analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, were discovered.{12336} This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels.{16245} N-Oleoyl taurine is an amino-acyl endocannabinoid isolated from rat brain that may activate TRPV1 and TRPV4.{16245}  

     

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    Cayman
    SKU:10005609 - 10 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine and N-arachidonoyl serine, have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomics analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, were discovered.{12336} This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels.{16245} N-Oleoyl taurine is an amino-acyl endocannabinoid isolated from rat brain that may activate TRPV1 and TRPV4.{16245}  

     

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    Cayman
    SKU:10005609 - 5 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine and N-arachidonoyl serine, have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomics analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, were discovered.{12336} This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels.{16245} N-Oleoyl taurine is an amino-acyl endocannabinoid isolated from rat brain that may activate TRPV1 and TRPV4.{16245}  

     

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    Cayman
    SKU:10005609 - 500 µg

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  • N-Oleoyl valine is an endogenous N-acyl amine that acts as an antagonist at the transient receptor potential vanilloid type 3 (TRPV3) receptor, which is involved in thermoregulation.{34195,34201} N-Oleoyl valine is increased in mice following cold exposure for up to at least 16 days.{31656} Acute lung injury in mice increases the concentration of N-Oleoyl valine in lung tissue.{34194} N-acyl amines also promote mitochondrial uncoupling.{31656}  

     

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    SKU:20065 -

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  • N-Oleoyl valine is an endogenous N-acyl amine that acts as an antagonist at the transient receptor potential vanilloid type 3 (TRPV3) receptor, which is involved in thermoregulation.{34195,34201} N-Oleoyl valine is increased in mice following cold exposure for up to at least 16 days.{31656} Acute lung injury in mice increases the concentration of N-Oleoyl valine in lung tissue.{34194} N-acyl amines also promote mitochondrial uncoupling.{31656}  

     

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    Cayman
    SKU:20065 -

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  • N-Oleoyl valine is an endogenous N-acyl amine that acts as an antagonist at the transient receptor potential vanilloid type 3 (TRPV3) receptor, which is involved in thermoregulation.{34195,34201} N-Oleoyl valine is increased in mice following cold exposure for up to at least 16 days.{31656} Acute lung injury in mice increases the concentration of N-Oleoyl valine in lung tissue.{34194} N-acyl amines also promote mitochondrial uncoupling.{31656}  

     

    Brand:
    Cayman
    SKU:20065 -

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  • N-Oleoyl valine is an endogenous N-acyl amine that acts as an antagonist at the transient receptor potential vanilloid type 3 (TRPV3) receptor, which is involved in thermoregulation.{34195,34201} N-Oleoyl valine is increased in mice following cold exposure for up to at least 16 days.{31656} Acute lung injury in mice increases the concentration of N-Oleoyl valine in lung tissue.{34194} N-acyl amines also promote mitochondrial uncoupling.{31656}  

     

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    Cayman
    SKU:20065 -

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  • N-Oleoyl-L-phenylalanine is an N-acyl amide.{31656} It increases the oxygen consumption rate (OCR) of mitochondria isolated from mouse brown adipose tissue in a Seahorse assay and decreases oligomycin-induced increases in the mitochondrial membrane potential in C2C12 cells, indicating mitochondrial uncoupling activity, when used at a concentration of 50 µM. N-Oleoyl-L-phenylalanine (30 mg/kg for eight days) reduces food intake and body weight of diet-induced obese mice.  

     

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    Cayman
    SKU:28921 - 1 mg

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  • N-Oleoyl-L-phenylalanine is an N-acyl amide.{31656} It increases the oxygen consumption rate (OCR) of mitochondria isolated from mouse brown adipose tissue in a Seahorse assay and decreases oligomycin-induced increases in the mitochondrial membrane potential in C2C12 cells, indicating mitochondrial uncoupling activity, when used at a concentration of 50 µM. N-Oleoyl-L-phenylalanine (30 mg/kg for eight days) reduces food intake and body weight of diet-induced obese mice.  

     

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    Cayman
    SKU:28921 - 10 mg

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  • N-Oleoyl-L-phenylalanine is an N-acyl amide.{31656} It increases the oxygen consumption rate (OCR) of mitochondria isolated from mouse brown adipose tissue in a Seahorse assay and decreases oligomycin-induced increases in the mitochondrial membrane potential in C2C12 cells, indicating mitochondrial uncoupling activity, when used at a concentration of 50 µM. N-Oleoyl-L-phenylalanine (30 mg/kg for eight days) reduces food intake and body weight of diet-induced obese mice.  

     

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    Cayman
    SKU:28921 - 5 mg

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  • Bone mass and shape is continuously remodeled by the concerted and balanced action of osteoblasts (bone forming cells) and osteoclasts (bone-resorbing cells). The endocannabinoid system plays an essential role in the maintenance of normal bone mass via signaling through the CB2 receptor.{16337} N-Oleoyl-L-serine is an endogenous lipid that has been reported to stimulate bone formation and to inhibit bone resorption.{16395}  

     

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    Cayman
    SKU:13058 - 1 mg

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  • Bone mass and shape is continuously remodeled by the concerted and balanced action of osteoblasts (bone forming cells) and osteoclasts (bone-resorbing cells). The endocannabinoid system plays an essential role in the maintenance of normal bone mass via signaling through the CB2 receptor.{16337} N-Oleoyl-L-serine is an endogenous lipid that has been reported to stimulate bone formation and to inhibit bone resorption.{16395}  

     

    Brand:
    Cayman
    SKU:13058 - 10 mg

    Available on backorder

  • Bone mass and shape is continuously remodeled by the concerted and balanced action of osteoblasts (bone forming cells) and osteoclasts (bone-resorbing cells). The endocannabinoid system plays an essential role in the maintenance of normal bone mass via signaling through the CB2 receptor.{16337} N-Oleoyl-L-serine is an endogenous lipid that has been reported to stimulate bone formation and to inhibit bone resorption.{16395}  

     

    Brand:
    Cayman
    SKU:13058 - 5 mg

    Available on backorder

  • Bone mass and shape is continuously remodeled by the concerted and balanced action of osteoblasts (bone forming cells) and osteoclasts (bone-resorbing cells). The endocannabinoid system plays an essential role in the maintenance of normal bone mass via signaling through the CB2 receptor.{16337} N-Oleoyl-L-serine is an endogenous lipid that has been reported to stimulate bone formation and to inhibit bone resorption.{16395}  

     

    Brand:
    Cayman
    SKU:13058 - 50 mg

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  • The jumonji domain-containing protein 2 (JMJD2) subfamily of histone demethylases have been shown to catalyze demethylation of the methylated forms of histone 3 lysine 9 (H3K9) and H3K36 in vitro and in cells.{19159} Because histone demethylases are implicated in certain diseases, including cancer, selective inhibitors are candidate anticancer agents as well as potential tools for elucidating the biological functions of JMJDs.{18098} N-Oxalylglycine, the amide analog of α-ketoglutarate, is a cell permeable inhibitor of α-ketoglutarate-dependent enzymes, including JMJD2A, JMJD2C, and JMJD2E (IC50s = 250, 500, and 24 μM, respectively).{18003,18511,18060,18061} It can also inhibit the prolyl hydroxylase domain-containing proteins PHD1 and PHD2 with IC50 values of 2.1 and 5.6 μM, respectively.{18511,18060, 18061}  

     

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  • The jumonji domain-containing protein 2 (JMJD2) subfamily of histone demethylases have been shown to catalyze demethylation of the methylated forms of histone 3 lysine 9 (H3K9) and H3K36 in vitro and in cells.{19159} Because histone demethylases are implicated in certain diseases, including cancer, selective inhibitors are candidate anticancer agents as well as potential tools for elucidating the biological functions of JMJDs.{18098} N-Oxalylglycine, the amide analog of α-ketoglutarate, is a cell permeable inhibitor of α-ketoglutarate-dependent enzymes, including JMJD2A, JMJD2C, and JMJD2E (IC50s = 250, 500, and 24 μM, respectively).{18003,18511,18060,18061} It can also inhibit the prolyl hydroxylase domain-containing proteins PHD1 and PHD2 with IC50 values of 2.1 and 5.6 μM, respectively.{18511,18060, 18061}  

     

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  • The jumonji domain-containing protein 2 (JMJD2) subfamily of histone demethylases have been shown to catalyze demethylation of the methylated forms of histone 3 lysine 9 (H3K9) and H3K36 in vitro and in cells.{19159} Because histone demethylases are implicated in certain diseases, including cancer, selective inhibitors are candidate anticancer agents as well as potential tools for elucidating the biological functions of JMJDs.{18098} N-Oxalylglycine, the amide analog of α-ketoglutarate, is a cell permeable inhibitor of α-ketoglutarate-dependent enzymes, including JMJD2A, JMJD2C, and JMJD2E (IC50s = 250, 500, and 24 μM, respectively).{18003,18511,18060,18061} It can also inhibit the prolyl hydroxylase domain-containing proteins PHD1 and PHD2 with IC50 values of 2.1 and 5.6 μM, respectively.{18511,18060, 18061}  

     

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    Cayman
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  • The jumonji domain-containing protein 2 (JMJD2) subfamily of histone demethylases have been shown to catalyze demethylation of the methylated forms of histone 3 lysine 9 (H3K9) and H3K36 in vitro and in cells.{19159} Because histone demethylases are implicated in certain diseases, including cancer, selective inhibitors are candidate anticancer agents as well as potential tools for elucidating the biological functions of JMJDs.{18098} N-Oxalylglycine, the amide analog of α-ketoglutarate, is a cell permeable inhibitor of α-ketoglutarate-dependent enzymes, including JMJD2A, JMJD2C, and JMJD2E (IC50s = 250, 500, and 24 μM, respectively).{18003,18511,18060,18061} It can also inhibit the prolyl hydroxylase domain-containing proteins PHD1 and PHD2 with IC50 values of 2.1 and 5.6 μM, respectively.{18511,18060, 18061}  

     

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    Cayman
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  • N-p-Tosyl-Gly-Pro-Lys-pNA is a colorimetric substrate for plasmin.{61063,61064,61065} Plasmin binds and hydrolyzes N-p-tosyl-Gly-Pro-Lys-pNA to release p-nitroanilide (pNA), which can be quantified by colorimetric detection at 405 nm as a measure of plasmin activity.  

     

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    SKU:31544 - 1 mg

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  • N-p-Tosyl-Gly-Pro-Lys-pNA is a colorimetric substrate for plasmin.{61063,61064,61065} Plasmin binds and hydrolyzes N-p-tosyl-Gly-Pro-Lys-pNA to release p-nitroanilide (pNA), which can be quantified by colorimetric detection at 405 nm as a measure of plasmin activity.  

     

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    Cayman
    SKU:31544 - 10 mg

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  • N-p-Tosyl-Gly-Pro-Lys-pNA is a colorimetric substrate for plasmin.{61063,61064,61065} Plasmin binds and hydrolyzes N-p-tosyl-Gly-Pro-Lys-pNA to release p-nitroanilide (pNA), which can be quantified by colorimetric detection at 405 nm as a measure of plasmin activity.  

     

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    SKU:31544 - 5 mg

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  • Several different fatty acyl dopamine analogs, such as N-arachidonoyl dopamine (NADA), N-oleoyl dopamine (ODA) and N-palmitoyl dopamine (PALDA), have been isolated and characterized from bovine brain.{9589,11117} Structurally, PALDA is the amide of palmitic acid and dopamine and is therefore a “hybrid” analog which incorporates components of both the anandamide-like and dopamine neurotransmitter pathways. Unlike NADA and ODA, PALDA is nearly inactive as a vanilloid receptor 1 (VR1) ligand and fails to elicit hyperalgesic or nocifensive responses in vivo.{11117} However, PALDA exhibits an “entourage” effect at concentrations of 0.1-10 µM by potentiating the VR1-mediated effects of NADA and anandamide.{13227}  

     

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    SKU:10007697 - 10 mg

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  • Several different fatty acyl dopamine analogs, such as N-arachidonoyl dopamine (NADA), N-oleoyl dopamine (ODA) and N-palmitoyl dopamine (PALDA), have been isolated and characterized from bovine brain.{9589,11117} Structurally, PALDA is the amide of palmitic acid and dopamine and is therefore a “hybrid” analog which incorporates components of both the anandamide-like and dopamine neurotransmitter pathways. Unlike NADA and ODA, PALDA is nearly inactive as a vanilloid receptor 1 (VR1) ligand and fails to elicit hyperalgesic or nocifensive responses in vivo.{11117} However, PALDA exhibits an “entourage” effect at concentrations of 0.1-10 µM by potentiating the VR1-mediated effects of NADA and anandamide.{13227}  

     

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    Cayman
    SKU:10007697 - 100 mg

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  • Several different fatty acyl dopamine analogs, such as N-arachidonoyl dopamine (NADA), N-oleoyl dopamine (ODA) and N-palmitoyl dopamine (PALDA), have been isolated and characterized from bovine brain.{9589,11117} Structurally, PALDA is the amide of palmitic acid and dopamine and is therefore a “hybrid” analog which incorporates components of both the anandamide-like and dopamine neurotransmitter pathways. Unlike NADA and ODA, PALDA is nearly inactive as a vanilloid receptor 1 (VR1) ligand and fails to elicit hyperalgesic or nocifensive responses in vivo.{11117} However, PALDA exhibits an “entourage” effect at concentrations of 0.1-10 µM by potentiating the VR1-mediated effects of NADA and anandamide.{13227}  

     

    Brand:
    Cayman
    SKU:10007697 - 5 mg

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  • Several different fatty acyl dopamine analogs, such as N-arachidonoyl dopamine (NADA), N-oleoyl dopamine (ODA) and N-palmitoyl dopamine (PALDA), have been isolated and characterized from bovine brain.{9589,11117} Structurally, PALDA is the amide of palmitic acid and dopamine and is therefore a “hybrid” analog which incorporates components of both the anandamide-like and dopamine neurotransmitter pathways. Unlike NADA and ODA, PALDA is nearly inactive as a vanilloid receptor 1 (VR1) ligand and fails to elicit hyperalgesic or nocifensive responses in vivo.{11117} However, PALDA exhibits an “entourage” effect at concentrations of 0.1-10 µM by potentiating the VR1-mediated effects of NADA and anandamide.{13227}  

     

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    SKU:10007697 - 50 mg

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  • The acyl amides are a family of endogenous lipids that act as potent modulators of pain and inflammation. The best characterized members of this family are the arachidonoyl amides, which includes N-arachidonoyl ethanolamide (AEA; anandamide). N-palmitoyl glycine (PalGly) contains an 18-carbon saturated fatty acid that is amide-linked to glycine and is structurally similar to the phospholipid-derived N-acyl ethanolamines. Endogenously produced in rat skin and spinal cord, PalGly is present in 100-fold greater amounts in skin and 3-fold greater in brain compared to AEA.{15693} Injection of 0.43 µg PalGly in rat hindpaw inhibits heat-induced firing of nociceptive neurons in rat dorsal horn.{15693} PalGly treatment induces transient calcium influx in native dorsal root ganglion (DRG) cells and in the PTX-sensitive, DRG-like cell line F-11 (EC50 = 5.5 µM).{15693}  

     

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    SKU:10009020 - 10 mg

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  • The acyl amides are a family of endogenous lipids that act as potent modulators of pain and inflammation. The best characterized members of this family are the arachidonoyl amides, which includes N-arachidonoyl ethanolamide (AEA; anandamide). N-palmitoyl glycine (PalGly) contains an 18-carbon saturated fatty acid that is amide-linked to glycine and is structurally similar to the phospholipid-derived N-acyl ethanolamines. Endogenously produced in rat skin and spinal cord, PalGly is present in 100-fold greater amounts in skin and 3-fold greater in brain compared to AEA.{15693} Injection of 0.43 µg PalGly in rat hindpaw inhibits heat-induced firing of nociceptive neurons in rat dorsal horn.{15693} PalGly treatment induces transient calcium influx in native dorsal root ganglion (DRG) cells and in the PTX-sensitive, DRG-like cell line F-11 (EC50 = 5.5 µM).{15693}  

     

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    Cayman
    SKU:10009020 - 100 mg

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  • The acyl amides are a family of endogenous lipids that act as potent modulators of pain and inflammation. The best characterized members of this family are the arachidonoyl amides, which includes N-arachidonoyl ethanolamide (AEA; anandamide). N-palmitoyl glycine (PalGly) contains an 18-carbon saturated fatty acid that is amide-linked to glycine and is structurally similar to the phospholipid-derived N-acyl ethanolamines. Endogenously produced in rat skin and spinal cord, PalGly is present in 100-fold greater amounts in skin and 3-fold greater in brain compared to AEA.{15693} Injection of 0.43 µg PalGly in rat hindpaw inhibits heat-induced firing of nociceptive neurons in rat dorsal horn.{15693} PalGly treatment induces transient calcium influx in native dorsal root ganglion (DRG) cells and in the PTX-sensitive, DRG-like cell line F-11 (EC50 = 5.5 µM).{15693}  

     

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    Cayman
    SKU:10009020 - 50 mg

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  • The acyl amides are a family of endogenous lipids that act as potent modulators of pain and inflammation. The best characterized members of this family are the arachidonoyl amides, which includes N-arachidonoyl ethanolamide (AEA; anandamide). N-palmitoyl glycine (PalGly) contains an 18-carbon saturated fatty acid that is amide-linked to glycine and is structurally similar to the phospholipid-derived N-acyl ethanolamines. Endogenously produced in rat skin and spinal cord, PalGly is present in 100-fold greater amounts in skin and 3-fold greater in brain compared to AEA.{15693} Injection of 0.43 µg PalGly in rat hindpaw inhibits heat-induced firing of nociceptive neurons in rat dorsal horn.{15693} PalGly treatment induces transient calcium influx in native dorsal root ganglion (DRG) cells and in the PTX-sensitive, DRG-like cell line F-11 (EC50 = 5.5 µM).{15693}  

     

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    SKU:10009020 - 500 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine (NADA) and N-arachidonoyl serine (ARA-S), have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomic analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, was discovered. N-Palmitoyl taurine is a prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling. Its function is currently under investigation.  

     

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    SKU:10005611 - 1 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine (NADA) and N-arachidonoyl serine (ARA-S), have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomic analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, was discovered. N-Palmitoyl taurine is a prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling. Its function is currently under investigation.  

     

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    Cayman
    SKU:10005611 - 10 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine (NADA) and N-arachidonoyl serine (ARA-S), have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomic analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, was discovered. N-Palmitoyl taurine is a prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling. Its function is currently under investigation.  

     

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    SKU:10005611 - 5 mg

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  • N-Palmitoyl-L-aspartate is a natural N-acylaspartate that inhibits Hedgehog signaling after stimulation with Smoothened agonist (SAG; Item No. 11914) or non-sterol-modified Sonic Hedgehog.{31541} It does not alter the activity of cannabinoid receptors or fatty acid amide hydrolase.{31541}  

     

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    SKU:19952 -

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  • N-Palmitoyl-L-aspartate is a natural N-acylaspartate that inhibits Hedgehog signaling after stimulation with Smoothened agonist (SAG; Item No. 11914) or non-sterol-modified Sonic Hedgehog.{31541} It does not alter the activity of cannabinoid receptors or fatty acid amide hydrolase.{31541}  

     

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    Cayman
    SKU:19952 -

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  • N-Palmitoyl-L-aspartate is a natural N-acylaspartate that inhibits Hedgehog signaling after stimulation with Smoothened agonist (SAG; Item No. 11914) or non-sterol-modified Sonic Hedgehog.{31541} It does not alter the activity of cannabinoid receptors or fatty acid amide hydrolase.{31541}  

     

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    Cayman
    SKU:19952 -

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  • N-Palmitoyl-L-aspartate is a natural N-acylaspartate that inhibits Hedgehog signaling after stimulation with Smoothened agonist (SAG; Item No. 11914) or non-sterol-modified Sonic Hedgehog.{31541} It does not alter the activity of cannabinoid receptors or fatty acid amide hydrolase.{31541}  

     

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    Cayman
    SKU:19952 -

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C15-HSL is a product of Y. pseudituberculosis.{15932}  

     

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C15-HSL is a product of Y. pseudituberculosis.{15932}  

     

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C15-HSL is a product of Y. pseudituberculosis.{15932}  

     

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C15-HSL is a product of Y. pseudituberculosis.{15932}  

     

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  • Quorum sensing is a regulatory system 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. Autoinducers containing a phenylacetanoyl group in the acyl chain display a wide range of inhibitory and activating effects on various R protein transcriptional regulators.{26043,26044,15550} N-phenylacetyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa.{15550,26045} It has been reported to antagonize TraR signaling in A. tumefaciens, LasR signaling in E. coli, and LuxR signaling in V. fischeri.{26044}  

     

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    SKU:9001737 - 1 mg

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  • Quorum sensing is a regulatory system 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. Autoinducers containing a phenylacetanoyl group in the acyl chain display a wide range of inhibitory and activating effects on various R protein transcriptional regulators.{26043,26044,15550} N-phenylacetyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa.{15550,26045} It has been reported to antagonize TraR signaling in A. tumefaciens, LasR signaling in E. coli, and LuxR signaling in V. fischeri.{26044}  

     

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    SKU:9001737 - 10 mg

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  • Quorum sensing is a regulatory system 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. Autoinducers containing a phenylacetanoyl group in the acyl chain display a wide range of inhibitory and activating effects on various R protein transcriptional regulators.{26043,26044,15550} N-phenylacetyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa.{15550,26045} It has been reported to antagonize TraR signaling in A. tumefaciens, LasR signaling in E. coli, and LuxR signaling in V. fischeri.{26044}  

     

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    Cayman
    SKU:9001737 - 25 mg

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  • Quorum sensing is a regulatory system 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. Autoinducers containing a phenylacetanoyl group in the acyl chain display a wide range of inhibitory and activating effects on various R protein transcriptional regulators.{26043,26044,15550} N-phenylacetyl-L-Homoserine lactone is a small diffusible signaling molecule involved in quorum sensing in the model symbiont V. fischeri and the pathogens A. tumefaciens and P. aeruginosa.{15550,26045} It has been reported to antagonize TraR signaling in A. tumefaciens, LasR signaling in E. coli, and LuxR signaling in V. fischeri.{26044}  

     

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    SKU:9001737 - 5 mg

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  • N-Phenylacetyl-L-prolylglycine ethyl ester is a synthetic dipeptide that has been shown to produce positive nootropic and cognitive effects in animal models (0.01-0.8 mg/kg) by a mechanism similar to other related racetam compounds.{24753} It can rescue neuroblastoma SH-SY5Y cells from amyloid-induced cytotoxicity, indicating a potential application in the treatment of neurodegenerative diseases.{24754} It also demonstrates antioxidant and anti-inflammatory effects, which have been examined in the context of an anti-diabetic agent.{24755} This compound was recently identified in illegal designer herbal products distributed in Japan and is intended for research and forensic purposes only.{23615}  

     

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  • N-Phenylacetyl-L-prolylglycine ethyl ester is a synthetic dipeptide that has been shown to produce positive nootropic and cognitive effects in animal models (0.01-0.8 mg/kg) by a mechanism similar to other related racetam compounds.{24753} It can rescue neuroblastoma SH-SY5Y cells from amyloid-induced cytotoxicity, indicating a potential application in the treatment of neurodegenerative diseases.{24754} It also demonstrates antioxidant and anti-inflammatory effects, which have been examined in the context of an anti-diabetic agent.{24755} This compound was recently identified in illegal designer herbal products distributed in Japan and is intended for research and forensic purposes only.{23615}  

     

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  • N-Phenylacetyl-L-prolylglycine ethyl ester is a synthetic dipeptide that has been shown to produce positive nootropic and cognitive effects in animal models (0.01-0.8 mg/kg) by a mechanism similar to other related racetam compounds.{24753} It can rescue neuroblastoma SH-SY5Y cells from amyloid-induced cytotoxicity, indicating a potential application in the treatment of neurodegenerative diseases.{24754} It also demonstrates antioxidant and anti-inflammatory effects, which have been examined in the context of an anti-diabetic agent.{24755} This compound was recently identified in illegal designer herbal products distributed in Japan and is intended for research and forensic purposes only.{23615}  

     

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  • N-Phenylpiperidin-4-amine is a building block.{56192} It has been used in the synthesis of M. tuberculosis decaprenylphosphoryl-β-D-ribose 2′-epimerase (DprE1) inhibitors.  

     

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    SKU:30898 - 1 mg

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  • N-Phenylpiperidin-4-amine is a building block.{56192} It has been used in the synthesis of M. tuberculosis decaprenylphosphoryl-β-D-ribose 2′-epimerase (DprE1) inhibitors.  

     

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    SKU:30898 - 10 mg

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  • N-Phenylpiperidin-4-amine is a building block.{56192} It has been used in the synthesis of M. tuberculosis decaprenylphosphoryl-β-D-ribose 2′-epimerase (DprE1) inhibitors.  

     

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    SKU:30898 - 5 mg

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  • N-Phenylthiourea is a tyrosinase inhibitor (Ki = 0.21 μM in an enzyme assay using L-DOPA as a substrate) and building block.{52758,52759} It increases the susceptibility of SK-MEL-188 melanoma cells in melanogenesis-inducing conditions to γ-radiation-induced cytotoxicity when used at a concentration of 0.01 μM.{52760} N-Phenylthiourea has been used as a precursor in the synthesis of compounds with antibacterial and antifungal activities.{52759} It has also been used as a genetic marker for taste because only some people detect it as a bitter taste.{22286}  

     

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    SKU:30855 - 100 g

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  • N-Phenylthiourea is a tyrosinase inhibitor (Ki = 0.21 μM in an enzyme assay using L-DOPA as a substrate) and building block.{52758,52759} It increases the susceptibility of SK-MEL-188 melanoma cells in melanogenesis-inducing conditions to γ-radiation-induced cytotoxicity when used at a concentration of 0.01 μM.{52760} N-Phenylthiourea has been used as a precursor in the synthesis of compounds with antibacterial and antifungal activities.{52759} It has also been used as a genetic marker for taste because only some people detect it as a bitter taste.{22286}  

     

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    SKU:30855 - 25 g

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  • N-Phenylthiourea is a tyrosinase inhibitor (Ki = 0.21 μM in an enzyme assay using L-DOPA as a substrate) and building block.{52758,52759} It increases the susceptibility of SK-MEL-188 melanoma cells in melanogenesis-inducing conditions to γ-radiation-induced cytotoxicity when used at a concentration of 0.01 μM.{52760} N-Phenylthiourea has been used as a precursor in the synthesis of compounds with antibacterial and antifungal activities.{52759} It has also been used as a genetic marker for taste because only some people detect it as a bitter taste.{22286}  

     

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    SKU:30855 - 250 g

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  • N-Phenylthiourea is a tyrosinase inhibitor (Ki = 0.21 μM in an enzyme assay using L-DOPA as a substrate) and building block.{52758,52759} It increases the susceptibility of SK-MEL-188 melanoma cells in melanogenesis-inducing conditions to γ-radiation-induced cytotoxicity when used at a concentration of 0.01 μM.{52760} N-Phenylthiourea has been used as a precursor in the synthesis of compounds with antibacterial and antifungal activities.{52759} It has also been used as a genetic marker for taste because only some people detect it as a bitter taste.{22286}  

     

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    SKU:30855 - 50 g

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  • N-Pivaloylaniline is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    SKU:10007092 - 1 g

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  • N-Pivaloylaniline is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    SKU:10007092 - 10 g

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  • N-Pivaloylaniline is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    SKU:10007092 - 5 g

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  • N-Pivaloylaniline is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    SKU:10007092 - 500 mg

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  • N-propyl Hexylone (hydrochloride) (Item No. 27078) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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    SKU:27078 - 1 mg

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  • N-propyl Hexylone (hydrochloride) (Item No. 27078) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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    SKU:27078 - 5 mg

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  • N-Propylamphetamine is an N-substituted amphetamine with a propyl group on the amphetamine backbone. It has about one-fourth the potency of N-ethylamphetamine (Item No. 11557) in impairing the performance of rats in various tests.{26035} The toxicological properties of this compound are not known. This product is intended for forensic and research applications.  

     

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  • N-Propylamphetamine is an N-substituted amphetamine with a propyl group on the amphetamine backbone. It has about one-fourth the potency of N-ethylamphetamine (Item No. 11557) in impairing the performance of rats in various tests.{26035} The toxicological properties of this compound are not known. This product is intended for forensic and research applications.  

     

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  • N-Propylamphetamine is an N-substituted amphetamine with a propyl group on the amphetamine backbone. It has about one-fourth the potency of N-ethylamphetamine (Item No. 11557) in impairing the performance of rats in various tests.{26035} The toxicological properties of this compound are not known. This product is intended for forensic and research applications.  

     

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine (NADA) and N-arachidonoyl serine (ARA-S), have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomic analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, was discovered.{12484} This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels.{16245} N-Stearoyl taurine is a prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling.{16245}  

     

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    SKU:10005610 - 1 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine (NADA) and N-arachidonoyl serine (ARA-S), have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomic analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, was discovered.{12484} This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels.{16245} N-Stearoyl taurine is a prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling.{16245}  

     

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    SKU:10005610 - 10 mg

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  • Several different arachidonoyl amino acids, including N-arachidonoyl dopamine (NADA) and N-arachidonoyl serine (ARA-S), have been isolated and characterized from bovine brain.{9589} During mass spectral lipidomic analysis of rat brain, a series of fatty acyl amides of a third amino acid, taurine, was discovered.{12484} This novel class of compounds is present in kidney and activates members of the transient receptor potential (TRP) family of calcium channels.{16245} N-Stearoyl taurine is a prominent amino-acyl endocannabinoid isolated from rat brain during lipidomics profiling.{16245}  

     

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    SKU:10005610 - 5 mg

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  • N-tert-butyl-α-Phenylnitrone (PBN) is a cell permeable spin trap commonly used in free radical research.{9996} It protects against oxidative damage caused by various inflammatory events, demonstrating neuroprotective, anti-anging, and antidiabetic effects.{9453} At millimolar concentrations, PBN has been shown to inhibit LPS-induced NF-κB DNA binding activity and inhibits COX-2 catalytic activity.{7405}  

     

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  • N-tert-butyl-α-Phenylnitrone (PBN) is a cell permeable spin trap commonly used in free radical research.{9996} It protects against oxidative damage caused by various inflammatory events, demonstrating neuroprotective, anti-anging, and antidiabetic effects.{9453} At millimolar concentrations, PBN has been shown to inhibit LPS-induced NF-κB DNA binding activity and inhibits COX-2 catalytic activity.{7405}  

     

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  • 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 LuxR family of proteins, is coordinated by the synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-tetradecanoyl-L-Homoserine lactone (C14-HSL) is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism in bacteria.{16305,16307,16308} It appears later than shorter acyl chain AHLs in developing biofilms{16592} and, like other long chain AHLs, stimulates bacterial growth.{16595} C14-HSL also alters the proteolytic activity and enhances the migration of some strains of Proteus mirabilis.{16596}  

     

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    SKU:10011200 - 10 mg

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  • 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 LuxR family of proteins, is coordinated by the synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-tetradecanoyl-L-Homoserine lactone (C14-HSL) is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism in bacteria.{16305,16307,16308} It appears later than shorter acyl chain AHLs in developing biofilms{16592} and, like other long chain AHLs, stimulates bacterial growth.{16595} C14-HSL also alters the proteolytic activity and enhances the migration of some strains of Proteus mirabilis.{16596}  

     

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    Cayman
    SKU:10011200 - 25 mg

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  • 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 LuxR family of proteins, is coordinated by the synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-tetradecanoyl-L-Homoserine lactone (C14-HSL) is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism in bacteria.{16305,16307,16308} It appears later than shorter acyl chain AHLs in developing biofilms{16592} and, like other long chain AHLs, stimulates bacterial growth.{16595} C14-HSL also alters the proteolytic activity and enhances the migration of some strains of Proteus mirabilis.{16596}  

     

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    Cayman
    SKU:10011200 - 5 mg

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  • 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 LuxR family of proteins, is coordinated by the synthesis of diffusible acylhomoserine lactone (AHL) molecules. N-tetradecanoyl-L-Homoserine lactone (C14-HSL) is a small diffusible signaling molecule involved in quorum sensing, thereby controlling gene expression and affecting cellular metabolism in bacteria.{16305,16307,16308} It appears later than shorter acyl chain AHLs in developing biofilms{16592} and, like other long chain AHLs, stimulates bacterial growth.{16595} C14-HSL also alters the proteolytic activity and enhances the migration of some strains of Proteus mirabilis.{16596}  

     

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    SKU:10011200 - 50 mg

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  • N-trans-Feruloyltyramine is a phenolic amide originally isolated from S. melongena that has diverse biological activities, including anti-inflammatory, antioxidative, and antiproliferative properties.{45249} It decreases nitric oxide (NO) production (IC50 = 17.36 µM) and inducible NO synthase (iNOS) activity and increases NO scavenging without inducing cytotoxicity in LPS-stimulated BV-2 cells.{45250} It also scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in TLC autographic and spectrophotometric assays.{45251} N-trans-Feruloyltyramine inhibits proliferation of HeLa and L929 cells by 72.2 and 22%, respectively, when used at a concentration of 30 µg/ml.{45252}  

     

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    SKU:27459 - 1 mg

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  • N-trans-Feruloyltyramine is a phenolic amide originally isolated from S. melongena that has diverse biological activities, including anti-inflammatory, antioxidative, and antiproliferative properties.{45249} It decreases nitric oxide (NO) production (IC50 = 17.36 µM) and inducible NO synthase (iNOS) activity and increases NO scavenging without inducing cytotoxicity in LPS-stimulated BV-2 cells.{45250} It also scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in TLC autographic and spectrophotometric assays.{45251} N-trans-Feruloyltyramine inhibits proliferation of HeLa and L929 cells by 72.2 and 22%, respectively, when used at a concentration of 30 µg/ml.{45252}  

     

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    SKU:27459 - 5 mg

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  • n-Triacontanol is a plant growth regulator found in the plant cuticle waxes and in beeswax as the palmitate ester.{1050} n-Triacontanol has been reported to have growth enhancing properties when applied to the leaves of growing plants.{9609}  

     

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    SKU:88840 - 100 mg

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  • n-Triacontanol is a plant growth regulator found in the plant cuticle waxes and in beeswax as the palmitate ester.{1050} n-Triacontanol has been reported to have growth enhancing properties when applied to the leaves of growing plants.{9609}  

     

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    SKU:88840 - 25 mg

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  • n-Triacontanol is a plant growth regulator found in the plant cuticle waxes and in beeswax as the palmitate ester.{1050} n-Triacontanol has been reported to have growth enhancing properties when applied to the leaves of growing plants.{9609}  

     

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    SKU:88840 - 50 mg

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  • n-Triacontanol is a plant growth regulator found in the plant cuticle waxes and in beeswax as the palmitate ester.{1050} n-Triacontanol has been reported to have growth enhancing properties when applied to the leaves of growing plants.{9609}  

     

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    SKU:88840 - 500 mg

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} N-tridecanoyl-L-Homoserine lactone (C13-HSL) possesses a rare odd-numbered acyl carbon chain and is produced by wild-type and mutant strains of Y. pseudotuberculosis in trace amounts.{15932}  

     

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} N-tridecanoyl-L-Homoserine lactone (C13-HSL) possesses a rare odd-numbered acyl carbon chain and is produced by wild-type and mutant strains of Y. pseudotuberculosis in trace amounts.{15932}  

     

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} N-tridecanoyl-L-Homoserine lactone (C13-HSL) possesses a rare odd-numbered acyl carbon chain and is produced by wild-type and mutant strains of Y. pseudotuberculosis in trace amounts.{15932}  

     

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    Cayman
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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} N-tridecanoyl-L-Homoserine lactone (C13-HSL) possesses a rare odd-numbered acyl carbon chain and is produced by wild-type and mutant strains of Y. pseudotuberculosis in trace amounts.{15932}  

     

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    Cayman
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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C11-HSL possesses a rare odd-numbered acyl carbon chain and may be a minor quorum-sensing signaling molecule in P. aeruginosa strains.{16344}  

     

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C11-HSL possesses a rare odd-numbered acyl carbon chain and may be a minor quorum-sensing signaling molecule in P. aeruginosa strains.{16344}  

     

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C11-HSL possesses a rare odd-numbered acyl carbon chain and may be a minor quorum-sensing signaling molecule in P. aeruginosa strains.{16344}  

     

    Brand:
    Cayman
    SKU:-

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  • Quorum sensing is a regulatory system 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). Regulation of bacterial quorum sensing signaling systems to inhibit pathogenesis represents a new approach to antimicrobial therapy in the treatment of infectious diseases.{15369} 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} C11-HSL possesses a rare odd-numbered acyl carbon chain and may be a minor quorum-sensing signaling molecule in P. aeruginosa strains.{16344}  

     

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    Cayman
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  • N,N-DET (hydrochloride) (exempt preparation) (Item No. 22877) is an analytical reference standard categorized as a tryptamine. N,N-DET (hydrochloride) is regulated as a Schedule I compound in the United States. N,N-DET (hydrochloride) (exempt preparation) (Item No. 22877) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:22877 - 1 mg

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  • N,N-didesmethyl AH 7921 (Item No. 20281) is an analytical reference standard that is structurally categorized as an opioid metabolite. It is a predominant metabolite of AH 7921 (Item No. 12036) incubated with human liver microsomes that is also abundant in hydrolyzed urine case samples.{32486} The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:20281 -

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  • N,N-didesmethyl AH 7921 (Item No. 20281) is an analytical reference standard that is structurally categorized as an opioid metabolite. It is a predominant metabolite of AH 7921 (Item No. 12036) incubated with human liver microsomes that is also abundant in hydrolyzed urine case samples.{32486} The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:20281 -

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  • N,N-diethyl Hexylone (hydrochloride) (Item No. 28475) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:28475 - 1 mg

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  • N,N-diethyl Hexylone (hydrochloride) (Item No. 28475) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:28475 - 5 mg

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  • N,N-Diethylpentylone (hydrochloride) (Item No. 20801) is an analytical reference standard that is structurally classified as a cathinone. Its physiological and toxicological actions have not been characterized. This compound is for the forensic analysis of samples that may contain this compound.  

     

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    Cayman
    SKU:20801 -

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  • N,N-Diethylpentylone (hydrochloride) (Item No. 20801) is an analytical reference standard that is structurally classified as a cathinone. Its physiological and toxicological actions have not been characterized. This compound is for the forensic analysis of samples that may contain this compound.  

     

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    Cayman
    SKU:20801 -

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  • N,N-dimethyl Sphinganine (d18:0) is a sphingolipid that increases during development of L. donovani promastigotes.{38953}  

     

    Brand:
    Cayman
    SKU:22504 -

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  • N,N-dimethyl Sphinganine (d18:0) is a sphingolipid that increases during development of L. donovani promastigotes.{38953}  

     

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    Cayman
    SKU:22504 -

    Out of stock

  • N,N-dimethyl Sphinganine (d18:0) is a sphingolipid that increases during development of L. donovani promastigotes.{38953}  

     

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    Cayman
    SKU:22504 -

    Out of stock

  • N,N-dimethyl Sphingosine (d17:1) is a dimethylated form of the amino alcohol sphingosine (d17:1) (Item No. 10007902).  

     

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    Cayman
    SKU:22503 -

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  • N,N-dimethyl Sphingosine (d17:1) is a dimethylated form of the amino alcohol sphingosine (d17:1) (Item No. 10007902).  

     

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    Cayman
    SKU:22503 -

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  • N,N-dimethyl Sphingosine (d17:1) is a dimethylated form of the amino alcohol sphingosine (d17:1) (Item No. 10007902).  

     

    Brand:
    Cayman
    SKU:22503 -

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  • N,N-dimethyl Undecylamine N-oxide is an organic building block that may act as a surfactant.  

     

    Brand:
    Cayman
    SKU:20650 -

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  • N,N-dimethyl Undecylamine N-oxide is an organic building block that may act as a surfactant.  

     

    Brand:
    Cayman
    SKU:20650 -

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  • N,N-dimethyl Undecylamine N-oxide is an organic building block that may act as a surfactant.  

     

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    Cayman
    SKU:20650 -

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  • N,N-dimethyl-3,4-DMA (hydrochloride) (Item No. 30485) is an analytical reference standard categorized as an amphetamine. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:30485 - 1 mg

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  • N,N-dimethyl-3,4-DMA (hydrochloride) (Item No. 30485) is an analytical reference standard categorized as an amphetamine. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:30485 - 5 mg

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  • N,N-dimethyl-L-Valine is a synthetic intermediate useful for pharmaceutical synthesis.  

     

    Brand:
    Cayman
    SKU:10007091 - 1 g

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  • N,N-dimethyl-L-Valine is a synthetic intermediate useful for pharmaceutical synthesis.  

     

    Brand:
    Cayman
    SKU:10007091 - 100 mg

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  • N,N-dimethyl-L-Valine is a synthetic intermediate useful for pharmaceutical synthesis.  

     

    Brand:
    Cayman
    SKU:10007091 - 5 g

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  • N,N-dimethyl-L-Valine is a synthetic intermediate useful for pharmaceutical synthesis.  

     

    Brand:
    Cayman
    SKU:10007091 - 500 mg

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  • N,N-DMC is a psychotropic compound of the phenethylamine and cathinone classes. In behavioral studies involving rats, dimethylcathinone is slightly less potent than methcathinone and essentially equipotent with cathinone.{20224} This product is intended for forensic purposes.  

     

    Brand:
    Cayman
    SKU:9001144 - 10 mg

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  • N,N-DMC is a psychotropic compound of the phenethylamine and cathinone classes. In behavioral studies involving rats, dimethylcathinone is slightly less potent than methcathinone and essentially equipotent with cathinone.{20224} This product is intended for forensic purposes.  

     

    Brand:
    Cayman
    SKU:9001144 - 5 mg

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  • N,N-DMC is a psychotropic compound of the phenethylamine and cathinone classes. In behavioral studies involving rats, dimethylcathinone is slightly less potent than methcathinone and essentially equipotent with cathinone.{20224} This product is intended for forensic purposes.  

     

    Brand:
    Cayman
    SKU:9001144 - 50 mg

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  • N,N-Dimethylphenethylamine (hydrochloride) (Item No. 29754) is an analytical reference standard categorized as a phenethylamine. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:29754 - 100 mg

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  • N,N-Dimethylphenethylamine (hydrochloride) (Item No. 29754) is an analytical reference standard categorized as a phenethylamine. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:29754 - 25 mg

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  • N,N-Dimethylsphingosine is a metabolite of sphingosine and an inhibitor of sphingosine kinase (SPHK) with Ki values of 3.1, 6.8, and 2.3 µM in U937, PC12, and Swiss 3T3 cell extracts, respectively.{6899,6900} It is selective for SPHK over PKC in PC12 cells when used at a concentration of 10 µM.{6900}  

     

    Brand:
    Cayman
    SKU:62575 - 10 mg

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  • N,N-Dimethylsphingosine is a metabolite of sphingosine and an inhibitor of sphingosine kinase (SPHK) with Ki values of 3.1, 6.8, and 2.3 µM in U937, PC12, and Swiss 3T3 cell extracts, respectively.{6899,6900} It is selective for SPHK over PKC in PC12 cells when used at a concentration of 10 µM.{6900}  

     

    Brand:
    Cayman
    SKU:62575 - 25 mg

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  • N,N-Dimethylsphingosine is a metabolite of sphingosine and an inhibitor of sphingosine kinase (SPHK) with Ki values of 3.1, 6.8, and 2.3 µM in U937, PC12, and Swiss 3T3 cell extracts, respectively.{6899,6900} It is selective for SPHK over PKC in PC12 cells when used at a concentration of 10 µM.{6900}  

     

    Brand:
    Cayman
    SKU:62575 - 5 mg

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  • N,N-Dimethylsphingosine is a metabolite of sphingosine and an inhibitor of sphingosine kinase (SPHK) with Ki values of 3.1, 6.8, and 2.3 µM in U937, PC12, and Swiss 3T3 cell extracts, respectively.{6899,6900} It is selective for SPHK over PKC in PC12 cells when used at a concentration of 10 µM.{6900}  

     

    Brand:
    Cayman
    SKU:62575 - 50 mg

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  • N,N-Dipropyldopamine is a dopamine receptor agonist.{47698,47699,47700} It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 µmol/kg, respectively), as well as reduces homovanillic acid (HVA; Item No. 27307) levels in rat striatum when administered at a dose of 80 µmol/kg.{47698} N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.{47699,47700}  

     

    Brand:
    Cayman
    SKU:28937 - 1 mg

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  • N,N-Dipropyldopamine is a dopamine receptor agonist.{47698,47699,47700} It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 µmol/kg, respectively), as well as reduces homovanillic acid (HVA; Item No. 27307) levels in rat striatum when administered at a dose of 80 µmol/kg.{47698} N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.{47699,47700}  

     

    Brand:
    Cayman
    SKU:28937 - 10 mg

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  • N,N-Dipropyldopamine is a dopamine receptor agonist.{47698,47699,47700} It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 µmol/kg, respectively), as well as reduces homovanillic acid (HVA; Item No. 27307) levels in rat striatum when administered at a dose of 80 µmol/kg.{47698} N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.{47699,47700}  

     

    Brand:
    Cayman
    SKU:28937 - 25 mg

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  • N,N-Dipropyldopamine is a dopamine receptor agonist.{47698,47699,47700} It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 µmol/kg, respectively), as well as reduces homovanillic acid (HVA; Item No. 27307) levels in rat striatum when administered at a dose of 80 µmol/kg.{47698} N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.{47699,47700}  

     

    Brand:
    Cayman
    SKU:28937 - 5 mg

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  • N,N-Dimethylamphetamine (N,N-DMA) is a regulated stimulant that is an N-methylated analog of methamphetamine.{21548} It is often found as an impurity in preparations of methamphetamine.{21545,21546} DMA itself is less active and less neurotoxic than methamphetamine.{21548,21542} The metabolites of DMA that are detectable in human urine have been characterized.{21547,21544} This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:-
  • N,N-DMT (exempt preparation) (Item No. 15694) is an analytical reference standard categorized as a tryptamine.{21843} N,N-DMT substitutes for LSD (D-tartrate) (Item No. 28289) in a two-lever drug discrimination test. N,N-DMT is regulated as a Schedule I compound in the United States. N,N-DMT (exempt preparation) (Item No. 15694) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.  

     

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    Cayman
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  • N,N’-bis(2,3-Dihydroxybenzoyl)-O-L-seryl-L-dehydroalanine is a bis-catechol. It is a potential metabolite of the microbial metabolite N,N’-bis(2,3-dihydroxybenzoyl)-O-L-seryl-L-serine (Item No. 31778) based on the formation of dehydroalanine residues in serine-containing microbial peptides.{59655} At the time N,N’-bis(2,3-dihydroxybenzoyl)-O-L-seryl-L-dehydroalanine was made available for purchase, specific metabolism data had not been published. Contact us if updated information on this molecule is now available.  

     

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    Cayman
    SKU:31779 - 100 µg

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  • N,N’-bis(2,3-Dihydroxybenzoyl)-O-L-seryl-L-dehydroalanine is a bis-catechol. It is a potential metabolite of the microbial metabolite N,N’-bis(2,3-dihydroxybenzoyl)-O-L-seryl-L-serine (Item No. 31778) based on the formation of dehydroalanine residues in serine-containing microbial peptides.{59655} At the time N,N’-bis(2,3-dihydroxybenzoyl)-O-L-seryl-L-dehydroalanine was made available for purchase, specific metabolism data had not been published. Contact us if updated information on this molecule is now available.  

     

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    Cayman
    SKU:31779 - 500 µg

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  • N,N’-bis(2,3-Dihydroxybenzoyl)-O-L-seryl-L-serine is a microbial metabolite and degradation product of the bacterial siderophore enterobactin that has been found in Streptomyces and has anticancer activity.{54582,54583,54584} It inhibits invasion of 26-L5 murine colon cancer cells in a Matrigel™ assay with an IC50 value of 2.7 µM.{54582}  

     

    Brand:
    Cayman
    SKU:31778 - 100 µg

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  • N,N’-bis(2,3-Dihydroxybenzoyl)-O-L-seryl-L-serine is a microbial metabolite and degradation product of the bacterial siderophore enterobactin that has been found in Streptomyces and has anticancer activity.{54582,54583,54584} It inhibits invasion of 26-L5 murine colon cancer cells in a Matrigel™ assay with an IC50 value of 2.7 µM.{54582}  

     

    Brand:
    Cayman
    SKU:31778 - 500 µg

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  • N,N’-Diacetyl-L-cystine (DiNAC) is a disulfide dimer of N-acetylcysteine with immunomodulatory properties. Its intact disulfide bridge has been shown to be important for its ability to modify contact sensitivity/delayed hypersensitivity reactions in mice.{29628,29626} At 3 µM/kg/day, DiNAC also demonstrates anti-atherosclerotic effects, improving endothelial function in Watanabe heritable hyperlipidemic rabbits.{29626,29629,29627}  

     

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    Cayman
    SKU:-

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  • N,N’-Diacetyl-L-cystine (DiNAC) is a disulfide dimer of N-acetylcysteine with immunomodulatory properties. Its intact disulfide bridge has been shown to be important for its ability to modify contact sensitivity/delayed hypersensitivity reactions in mice.{29628,29626} At 3 µM/kg/day, DiNAC also demonstrates anti-atherosclerotic effects, improving endothelial function in Watanabe heritable hyperlipidemic rabbits.{29626,29629,29627}  

     

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    Cayman
    SKU:-

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  • N,N’-Diacetyl-L-cystine (DiNAC) is a disulfide dimer of N-acetylcysteine with immunomodulatory properties. Its intact disulfide bridge has been shown to be important for its ability to modify contact sensitivity/delayed hypersensitivity reactions in mice.{29628,29626} At 3 µM/kg/day, DiNAC also demonstrates anti-atherosclerotic effects, improving endothelial function in Watanabe heritable hyperlipidemic rabbits.{29626,29629,29627}  

     

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    Cayman
    SKU:-

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  • Epoxyeicosatrienoic acids (EETs), lipid mediators synthesized from arachidonic acid by cytochrome P-450 epoxygenases, are converted by soluble epoxide hydrolase (sEH) to the corresponding dihydroxyeicosatrienoic acids (DHETs). N,N’ Dicyclohexylurea (DCU) is a selective sEH inhibitor with IC50 values of 160 and 90 nM for recombinant human and mouse sEH, respectively.{12627} At 10 µM, DCU blocks the hydrolysis of cis- and trans-EETs by rat red blood cells and porcine coronary endothelial cells as well as completely inhibits 14,(15)-EET-induced PPARα activation.{17909,12613,17908}  

     

    Brand:
    Cayman
    SKU:10004971 - 10 g

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  • Epoxyeicosatrienoic acids (EETs), lipid mediators synthesized from arachidonic acid by cytochrome P-450 epoxygenases, are converted by soluble epoxide hydrolase (sEH) to the corresponding dihydroxyeicosatrienoic acids (DHETs). N,N’ Dicyclohexylurea (DCU) is a selective sEH inhibitor with IC50 values of 160 and 90 nM for recombinant human and mouse sEH, respectively.{12627} At 10 µM, DCU blocks the hydrolysis of cis- and trans-EETs by rat red blood cells and porcine coronary endothelial cells as well as completely inhibits 14,(15)-EET-induced PPARα activation.{17909,12613,17908}  

     

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    Cayman
    SKU:10004971 - 25 g

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  • N,N’,N”-Triacetylchitotriose is a triose oligosaccharide derived from chitin, consisting of three N-acetylglucosamine units. It has been shown to scavenge reactive oxygen species and to protect DNA from oxidative damage.{32543,32542}  

     

    Brand:
    Cayman
    SKU:20759 -

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  • N,N’,N”-Triacetylchitotriose is a triose oligosaccharide derived from chitin, consisting of three N-acetylglucosamine units. It has been shown to scavenge reactive oxygen species and to protect DNA from oxidative damage.{32543,32542}  

     

    Brand:
    Cayman
    SKU:20759 -

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  • N,N’,N”-Triacetylchitotriose is a triose oligosaccharide derived from chitin, consisting of three N-acetylglucosamine units. It has been shown to scavenge reactive oxygen species and to protect DNA from oxidative damage.{32543,32542}  

     

    Brand:
    Cayman
    SKU:20759 -

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  • N,N’-bis-Cbz-β-Alethine is an active ester used in the synthesis of β-alethine, which induces cell differentiation and has potential anti-tumor applications.{34526,34527,34528} β-Alethine is synthesized by removing the carbobenzoxy (CBZ) groups with hydrogen bromide in glacial acetic acid.{34526,34527,34528}  

     

    Brand:
    Cayman
    SKU:20878 -

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  • N,N’-bis-Cbz-β-Alethine is an active ester used in the synthesis of β-alethine, which induces cell differentiation and has potential anti-tumor applications.{34526,34527,34528} β-Alethine is synthesized by removing the carbobenzoxy (CBZ) groups with hydrogen bromide in glacial acetic acid.{34526,34527,34528}  

     

    Brand:
    Cayman
    SKU:20878 -

    Out of stock

  • N,N’-bis-Cbz-β-Alethine is an active ester used in the synthesis of β-alethine, which induces cell differentiation and has potential anti-tumor applications.{34526,34527,34528} β-Alethine is synthesized by removing the carbobenzoxy (CBZ) groups with hydrogen bromide in glacial acetic acid.{34526,34527,34528}  

     

    Brand:
    Cayman
    SKU:20878 -

    Out of stock

  • N,N’-bis-Cbz-β-Alethine is an active ester used in the synthesis of β-alethine, which induces cell differentiation and has potential anti-tumor applications.{34526,34527,34528} β-Alethine is synthesized by removing the carbobenzoxy (CBZ) groups with hydrogen bromide in glacial acetic acid.{34526,34527,34528}  

     

    Brand:
    Cayman
    SKU:20878 -

    Out of stock

  • N,O-Diacetyltyramine is a fungal metabolite that has been found in P. endophytica and has diverse biological activities.{54018} It is active against a panel of 13 bacteria (MICs = 8-128 µg/ml), as well as a panel of nine fungi (MICs = 64-256 µg/ml). N,O-Diacetyltyramine is cytotoxic to MDA-MB-231, HeLa, MCF-7, and OAW42 cancer cells when used at concentrations ranging from 10 to 5,000 nM. It is larvicidal against A. aegypti, A. albimanus, and C. quinquefasciatus mosquitos (LC50s = 724.8, 403.1, and 506.7 ppm, respectively).{54019}  

     

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    Cayman
    SKU:28738 - 1 mg

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  • N1-Acetylspermidine is an acetyl derivative of spermidine (Item No. 14918) that acts as a substrate for polyamine oxidase (PAO).{26260} In peroxisomes, PAO oxidizes N1-acetylspermidine to 3-acetamidopropanal and putrescine, a positively charged polyamine that binds DNA and is involved in various cellular processes including cell division, differentiation, and membrane function.{26259,23742,23743,12989} N1-Acetylspermidine has been used to examine the interaction between DNA and polyamines during the cleavage of phosphodiester bonds at apurinic/apyrimidinic sites in DNA.{27034}  

     

    Brand:
    Cayman
    SKU:9001535 - 1 mg

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  • N1-Acetylspermidine is an acetyl derivative of spermidine (Item No. 14918) that acts as a substrate for polyamine oxidase (PAO).{26260} In peroxisomes, PAO oxidizes N1-acetylspermidine to 3-acetamidopropanal and putrescine, a positively charged polyamine that binds DNA and is involved in various cellular processes including cell division, differentiation, and membrane function.{26259,23742,23743,12989} N1-Acetylspermidine has been used to examine the interaction between DNA and polyamines during the cleavage of phosphodiester bonds at apurinic/apyrimidinic sites in DNA.{27034}  

     

    Brand:
    Cayman
    SKU:9001535 - 10 mg

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