Chemicals

Showing 28651–28800 of 41137 results

  • 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}  

     

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    SKU:9001535 - 5 mg

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  • N1-Acetylspermine is a monoacetylated derivative of spermine (Item No. 18041), an endogenous polyamine synthesized from spermidine (Item No. 14918), that displays lower Km and higher Vmax values than spermine, making it a better substrate of polyamine oxidase than the non-acetylated polyamine.{29261} Spermine is required for eukaryotic cell growth and protein synthesis and is involved in the modulation of calcium-dependent immune processes.{27553,29231} N1-Acetylspermine has been used to study the uptake of the anticancer polyamine analog bleomycin-A5 by the human carnitine transporter SLC22A16.{29262}  

     

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  • N1-Acetylspermine is a monoacetylated derivative of spermine (Item No. 18041), an endogenous polyamine synthesized from spermidine (Item No. 14918), that displays lower Km and higher Vmax values than spermine, making it a better substrate of polyamine oxidase than the non-acetylated polyamine.{29261} Spermine is required for eukaryotic cell growth and protein synthesis and is involved in the modulation of calcium-dependent immune processes.{27553,29231} N1-Acetylspermine has been used to study the uptake of the anticancer polyamine analog bleomycin-A5 by the human carnitine transporter SLC22A16.{29262}  

     

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  • N1-Methylguanosine (m1G) is a methylated purine nucleoside formed during the degradation of tRNA and a biological end product.{57306,57307} Levels of m1G are increased in the urine of patients with malignant tumors compared to those with benign or no tumors and have been used as biomarkers of cancer.{27865,57306}  

     

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    SKU:31737 - 1 mg

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  • N1-Methylguanosine (m1G) is a methylated purine nucleoside formed during the degradation of tRNA and a biological end product.{57306,57307} Levels of m1G are increased in the urine of patients with malignant tumors compared to those with benign or no tumors and have been used as biomarkers of cancer.{27865,57306}  

     

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    SKU:31737 - 10 mg

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  • N1-Methylguanosine (m1G) is a methylated purine nucleoside formed during the degradation of tRNA and a biological end product.{57306,57307} Levels of m1G are increased in the urine of patients with malignant tumors compared to those with benign or no tumors and have been used as biomarkers of cancer.{27865,57306}  

     

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    SKU:31737 - 25 mg

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  • N1-Methylguanosine (m1G) is a methylated purine nucleoside formed during the degradation of tRNA and a biological end product.{57306,57307} Levels of m1G are increased in the urine of patients with malignant tumors compared to those with benign or no tumors and have been used as biomarkers of cancer.{27865,57306}  

     

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    SKU:31737 - 5 mg

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  • N1,N12-Acetylspermine is a diacetylated derivative of spermine (Item No. 18041), an endogenous polyamine synthesized from spermidine (Item No. 14918), that displays lower Km and higher Vmax values than spermine, making it a better substrate of polyamine oxidase than the non-acetylated polyamine.{29261} Spermine is required for eukaryotic cell growth and protein synthesis and is involved in the modulation of calcium-dependent immune processes.{27553,29231} Upregulation of N1,N12-acetylspermine has been linked to the incidence of cancer, making this natural polyamine a potential biomarker for cancer detection.{28930}  

     

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  • N1,N12-Acetylspermine is a diacetylated derivative of spermine (Item No. 18041), an endogenous polyamine synthesized from spermidine (Item No. 14918), that displays lower Km and higher Vmax values than spermine, making it a better substrate of polyamine oxidase than the non-acetylated polyamine.{29261} Spermine is required for eukaryotic cell growth and protein synthesis and is involved in the modulation of calcium-dependent immune processes.{27553,29231} Upregulation of N1,N12-acetylspermine has been linked to the incidence of cancer, making this natural polyamine a potential biomarker for cancer detection.{28930}  

     

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  • N1,N12-Acetylspermine is a diacetylated derivative of spermine (Item No. 18041), an endogenous polyamine synthesized from spermidine (Item No. 14918), that displays lower Km and higher Vmax values than spermine, making it a better substrate of polyamine oxidase than the non-acetylated polyamine.{29261} Spermine is required for eukaryotic cell growth and protein synthesis and is involved in the modulation of calcium-dependent immune processes.{27553,29231} Upregulation of N1,N12-acetylspermine has been linked to the incidence of cancer, making this natural polyamine a potential biomarker for cancer detection.{28930}  

     

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  • N1,N12-Acetylspermine is a diacetylated derivative of spermine (Item No. 18041), an endogenous polyamine synthesized from spermidine (Item No. 14918), that displays lower Km and higher Vmax values than spermine, making it a better substrate of polyamine oxidase than the non-acetylated polyamine.{29261} Spermine is required for eukaryotic cell growth and protein synthesis and is involved in the modulation of calcium-dependent immune processes.{27553,29231} Upregulation of N1,N12-acetylspermine has been linked to the incidence of cancer, making this natural polyamine a potential biomarker for cancer detection.{28930}  

     

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  • N1,N8-Diacetylspermidine is a diacetylated derivative of spermidine (Item No. 14918), a natural polyamine.{38652,38651} N1,N8-Diacetylspermidine has been found in human urine and is elevated in the urine of patients with colorectal and urogenital malignancies. It is selectively elevated in those with malignant conditions over those with benign urogenital hyperplasias, making this polyamine a potential biomarker for cancer detection.  

     

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    SKU:21588 -

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  • N1,N8-Diacetylspermidine is a diacetylated derivative of spermidine (Item No. 14918), a natural polyamine.{38652,38651} N1,N8-Diacetylspermidine has been found in human urine and is elevated in the urine of patients with colorectal and urogenital malignancies. It is selectively elevated in those with malignant conditions over those with benign urogenital hyperplasias, making this polyamine a potential biomarker for cancer detection.  

     

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    SKU:21588 -

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  • N1,N8-Diacetylspermidine is a diacetylated derivative of spermidine (Item No. 14918), a natural polyamine.{38652,38651} N1,N8-Diacetylspermidine has been found in human urine and is elevated in the urine of patients with colorectal and urogenital malignancies. It is selectively elevated in those with malignant conditions over those with benign urogenital hyperplasias, making this polyamine a potential biomarker for cancer detection.  

     

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    SKU:21588 -

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  • N1,N8-Diacetylspermidine is a diacetylated derivative of spermidine (Item No. 14918), a natural polyamine.{38652,38651} N1,N8-Diacetylspermidine has been found in human urine and is elevated in the urine of patients with colorectal and urogenital malignancies. It is selectively elevated in those with malignant conditions over those with benign urogenital hyperplasias, making this polyamine a potential biomarker for cancer detection.  

     

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    SKU:21588 -

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  • N106 is an activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2A (SERCA2A) SUMOylation.{56159} It activates SUMO-activating enzyme E1, which increases SUMOylation and the activity of SERCA2A in isolated adult rat cardiomyocytes when used at concentrations ranging from 0.1 to 1 µM. N106 increases contractility in the same cells. In vivo, N106 (10 mg/kg) increases cardiac SERCA2A SUMOylation and contractility in a mouse model of pressure overload-induced heart failure.  

     

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    SKU:30952 - 1 mg

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  • N106 is an activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2A (SERCA2A) SUMOylation.{56159} It activates SUMO-activating enzyme E1, which increases SUMOylation and the activity of SERCA2A in isolated adult rat cardiomyocytes when used at concentrations ranging from 0.1 to 1 µM. N106 increases contractility in the same cells. In vivo, N106 (10 mg/kg) increases cardiac SERCA2A SUMOylation and contractility in a mouse model of pressure overload-induced heart failure.  

     

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    SKU:30952 - 10 mg

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  • N106 is an activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2A (SERCA2A) SUMOylation.{56159} It activates SUMO-activating enzyme E1, which increases SUMOylation and the activity of SERCA2A in isolated adult rat cardiomyocytes when used at concentrations ranging from 0.1 to 1 µM. N106 increases contractility in the same cells. In vivo, N106 (10 mg/kg) increases cardiac SERCA2A SUMOylation and contractility in a mouse model of pressure overload-induced heart failure.  

     

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    Cayman
    SKU:30952 - 25 mg

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  • N106 is an activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2A (SERCA2A) SUMOylation.{56159} It activates SUMO-activating enzyme E1, which increases SUMOylation and the activity of SERCA2A in isolated adult rat cardiomyocytes when used at concentrations ranging from 0.1 to 1 µM. N106 increases contractility in the same cells. In vivo, N106 (10 mg/kg) increases cardiac SERCA2A SUMOylation and contractility in a mouse model of pressure overload-induced heart failure.  

     

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    SKU:30952 - 5 mg

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  • N2-Isobutyryl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyguanosine is a building block that has been used in the synthesis of oligodeoxyribonucleotides.{54119,54118,54117}  

     

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    SKU:30472 - 100 mg

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  • N2-Isobutyryl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyguanosine is a building block that has been used in the synthesis of oligodeoxyribonucleotides.{54119,54118,54117}  

     

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    SKU:30472 - 250 mg

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  • N2-Isobutyryl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyguanosine is a building block that has been used in the synthesis of oligodeoxyribonucleotides.{54119,54118,54117}  

     

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    SKU:30472 - 50 mg

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  • N2-Isobutyryl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyguanosine is a building block that has been used in the synthesis of oligodeoxyribonucleotides.{54119,54118,54117}  

     

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    SKU:30472 - 500 mg

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  • N6-(Δ2-Isopentenyl)adenine is a naturally occurring cytokinin that regulates cell division, development, and nutrient processing in plants.{29070} It serves as a precursor to zeatin synthesis.{29068,29069}  

     

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  • N6-(Δ2-Isopentenyl)adenine is a naturally occurring cytokinin that regulates cell division, development, and nutrient processing in plants.{29070} It serves as a precursor to zeatin synthesis.{29068,29069}  

     

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  • N6-(Δ2-Isopentenyl)adenine is a naturally occurring cytokinin that regulates cell division, development, and nutrient processing in plants.{29070} It serves as a precursor to zeatin synthesis.{29068,29069}  

     

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  • N6-(Δ2-Isopentenyl)adenine is a naturally occurring cytokinin that regulates cell division, development, and nutrient processing in plants.{29070} It serves as a precursor to zeatin synthesis.{29068,29069}  

     

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  • N6-(Δ2-Isopentenyl)adenosine is a precursor in the biosynthesis of the plant hormone N6-(Δ2-isopentenyl)adenine (Item No. 17906).{17845} N6-(Δ2-isopentenyl)adenine may be converted to the cytokinin trans-zeatin (Item No. 13226) by cytochrome P450 mono-oxygenases.{17845} Cytokinins, including N6-(Δ2-isopentenyl)adenine and trans-zeatin, regulate diverse events in plant growth and development. N6-(Δ2-Isopentenyl)adenosine can also alter post-transcriptional processes in mammalian cells, altering proliferation and apoptosis.{32406,32407}  

     

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    SKU:20522 -

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  • N6-(Δ2-Isopentenyl)adenosine is a precursor in the biosynthesis of the plant hormone N6-(Δ2-isopentenyl)adenine (Item No. 17906).{17845} N6-(Δ2-isopentenyl)adenine may be converted to the cytokinin trans-zeatin (Item No. 13226) by cytochrome P450 mono-oxygenases.{17845} Cytokinins, including N6-(Δ2-isopentenyl)adenine and trans-zeatin, regulate diverse events in plant growth and development. N6-(Δ2-Isopentenyl)adenosine can also alter post-transcriptional processes in mammalian cells, altering proliferation and apoptosis.{32406,32407}  

     

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    SKU:20522 -

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  • N6-(Δ2-Isopentenyl)adenosine is a precursor in the biosynthesis of the plant hormone N6-(Δ2-isopentenyl)adenine (Item No. 17906).{17845} N6-(Δ2-isopentenyl)adenine may be converted to the cytokinin trans-zeatin (Item No. 13226) by cytochrome P450 mono-oxygenases.{17845} Cytokinins, including N6-(Δ2-isopentenyl)adenine and trans-zeatin, regulate diverse events in plant growth and development. N6-(Δ2-Isopentenyl)adenosine can also alter post-transcriptional processes in mammalian cells, altering proliferation and apoptosis.{32406,32407}  

     

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    Cayman
    SKU:20522 -

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  • N6-(Δ2-Isopentenyl)adenosine is a precursor in the biosynthesis of the plant hormone N6-(Δ2-isopentenyl)adenine (Item No. 17906).{17845} N6-(Δ2-isopentenyl)adenine may be converted to the cytokinin trans-zeatin (Item No. 13226) by cytochrome P450 mono-oxygenases.{17845} Cytokinins, including N6-(Δ2-isopentenyl)adenine and trans-zeatin, regulate diverse events in plant growth and development. N6-(Δ2-Isopentenyl)adenosine can also alter post-transcriptional processes in mammalian cells, altering proliferation and apoptosis.{32406,32407}  

     

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    SKU:20522 -

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  • N6-benzoyl-2′-Deoxyadenosine is a nucleoside building block.{49652,49653} It is amino-protected and has been used in the synthesis of various oligonucleotides.  

     

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    SKU:30262 - 1 g

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  • N6-benzoyl-2′-Deoxyadenosine is a nucleoside building block.{49652,49653} It is amino-protected and has been used in the synthesis of various oligonucleotides.  

     

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    SKU:30262 - 10 g

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  • N6-benzoyl-2′-Deoxyadenosine is a nucleoside building block.{49652,49653} It is amino-protected and has been used in the synthesis of various oligonucleotides.  

     

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    SKU:30262 - 25 g

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  • N6-benzoyl-2′-Deoxyadenosine is a nucleoside building block.{49652,49653} It is amino-protected and has been used in the synthesis of various oligonucleotides.  

     

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    SKU:30262 - 5 g

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  • N6-benzoyl-Cyclic AMP (6-Bnz-cAMP) is a cell permeable cAMP analog that selectively activates PKA over exchange proteins activated by cAMP (Epac1 and 2, also known as RAPGEF3 and 4).{26217} It binds the AI and AII subunits of PKA with pKi values of 4.0 and 3.8, respectively, whereas it binds Epac1 with a pKi value of 1.3.{28118} 6-Bnz-cAMP stimulates the phosphorylation of the PKA substrate CREB but does not activate the Epac target Rap1.{28118} It can act synergistically with Epac-selective activators, such as 8-pCPT-2’-O-Me-cAMP (Item No. 17143).{30350,28118}  

     

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  • N6-benzoyl-Cyclic AMP (6-Bnz-cAMP) is a cell permeable cAMP analog that selectively activates PKA over exchange proteins activated by cAMP (Epac1 and 2, also known as RAPGEF3 and 4).{26217} It binds the AI and AII subunits of PKA with pKi values of 4.0 and 3.8, respectively, whereas it binds Epac1 with a pKi value of 1.3.{28118} 6-Bnz-cAMP stimulates the phosphorylation of the PKA substrate CREB but does not activate the Epac target Rap1.{28118} It can act synergistically with Epac-selective activators, such as 8-pCPT-2’-O-Me-cAMP (Item No. 17143).{30350,28118}  

     

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  • N6-Benzyladenine (6-BAP) is a synthetic cytokinin that stimulates plant growth and regulates de novo bud development, leaf expansion, delay of senescence, and chloroplast formation in plants.{34424,34425} 6-BAP inhibits respiratory kinase in plants and increases post-harvest life of green vegetables.{34425,34423} 6-BAP also increases lipid and docosahexaenoic acid (DHA; Item No. 90310) production in Aurantiochytrium species.{34423} 6-BAP treatment of myeloid leukemia cells induces differentiation into granulocytes.{34422}  

     

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    SKU:21711 -

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  • N6-Benzyladenine (6-BAP) is a synthetic cytokinin that stimulates plant growth and regulates de novo bud development, leaf expansion, delay of senescence, and chloroplast formation in plants.{34424,34425} 6-BAP inhibits respiratory kinase in plants and increases post-harvest life of green vegetables.{34425,34423} 6-BAP also increases lipid and docosahexaenoic acid (DHA; Item No. 90310) production in Aurantiochytrium species.{34423} 6-BAP treatment of myeloid leukemia cells induces differentiation into granulocytes.{34422}  

     

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    SKU:21711 -

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  • N6-Benzyladenine (6-BAP) is a synthetic cytokinin that stimulates plant growth and regulates de novo bud development, leaf expansion, delay of senescence, and chloroplast formation in plants.{34424,34425} 6-BAP inhibits respiratory kinase in plants and increases post-harvest life of green vegetables.{34425,34423} 6-BAP also increases lipid and docosahexaenoic acid (DHA; Item No. 90310) production in Aurantiochytrium species.{34423} 6-BAP treatment of myeloid leukemia cells induces differentiation into granulocytes.{34422}  

     

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    SKU:21711 -

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  • N6-Benzyladenine (6-BAP) is a synthetic cytokinin that stimulates plant growth and regulates de novo bud development, leaf expansion, delay of senescence, and chloroplast formation in plants.{34424,34425} 6-BAP inhibits respiratory kinase in plants and increases post-harvest life of green vegetables.{34425,34423} 6-BAP also increases lipid and docosahexaenoic acid (DHA; Item No. 90310) production in Aurantiochytrium species.{34423} 6-BAP treatment of myeloid leukemia cells induces differentiation into granulocytes.{34422}  

     

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    SKU:21711 -

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  • N6-Cyclohexyladenosine is an adenosine receptor agonist.{48560} It selectively binds to adenosine A1 receptors in rat cortical membranes (IC50 = 2.3 nM) over A2 receptors in rat striatal membranes (IC50 = 870 nM). N6-Cyclohexyladenosine decreases heart rate and increases coronary flow in a perfused working rat heart model ex vivo (EC25s = 5 and 860 nM, respectively). In vivo, it decreases heart rate and blood pressure in normotensive rats (EC25s = 2.4 and 4.2 μg/kg, respectively).{48560} N6-Cyclohexyladenosine (100 μM) induces sleep in rats when administered via basal forebrain infusion.{52007} N6-Cyclohexyladenosine also decreases locomotor activity in mice (ED50 = 60 μg/kg, i.p.).{52008}  

     

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    SKU:28427 - 100 mg

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  • N6-Cyclohexyladenosine is an adenosine receptor agonist.{48560} It selectively binds to adenosine A1 receptors in rat cortical membranes (IC50 = 2.3 nM) over A2 receptors in rat striatal membranes (IC50 = 870 nM). N6-Cyclohexyladenosine decreases heart rate and increases coronary flow in a perfused working rat heart model ex vivo (EC25s = 5 and 860 nM, respectively). In vivo, it decreases heart rate and blood pressure in normotensive rats (EC25s = 2.4 and 4.2 μg/kg, respectively).{48560} N6-Cyclohexyladenosine (100 μM) induces sleep in rats when administered via basal forebrain infusion.{52007} N6-Cyclohexyladenosine also decreases locomotor activity in mice (ED50 = 60 μg/kg, i.p.).{52008}  

     

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    SKU:28427 - 25 mg

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  • N6-Cyclohexyladenosine is an adenosine receptor agonist.{48560} It selectively binds to adenosine A1 receptors in rat cortical membranes (IC50 = 2.3 nM) over A2 receptors in rat striatal membranes (IC50 = 870 nM). N6-Cyclohexyladenosine decreases heart rate and increases coronary flow in a perfused working rat heart model ex vivo (EC25s = 5 and 860 nM, respectively). In vivo, it decreases heart rate and blood pressure in normotensive rats (EC25s = 2.4 and 4.2 μg/kg, respectively).{48560} N6-Cyclohexyladenosine (100 μM) induces sleep in rats when administered via basal forebrain infusion.{52007} N6-Cyclohexyladenosine also decreases locomotor activity in mice (ED50 = 60 μg/kg, i.p.).{52008}  

     

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    SKU:28427 - 50 mg

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  • N6-Cyclopentyladenosine is a selective agonist at adenosine 1 receptors (A1Rs) (Kis = 2.3, 790, and 43 nM for A1R, A2R, and A3R receptors, respectively, in transfected CHO cells).{34118,27925} When microinjected into the rat brainstem, it increases blood pressure and heart rate.{34115} It is effective for pain in normal and nerve-injured rats and shows anticonvulsant activity in a rat model of generalized seizures.{34116,34117}  

     

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    SKU:21448 -

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  • N6-Cyclopentyladenosine is a selective agonist at adenosine 1 receptors (A1Rs) (Kis = 2.3, 790, and 43 nM for A1R, A2R, and A3R receptors, respectively, in transfected CHO cells).{34118,27925} When microinjected into the rat brainstem, it increases blood pressure and heart rate.{34115} It is effective for pain in normal and nerve-injured rats and shows anticonvulsant activity in a rat model of generalized seizures.{34116,34117}  

     

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    SKU:21448 -

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  • N6-Cyclopentyladenosine is a selective agonist at adenosine 1 receptors (A1Rs) (Kis = 2.3, 790, and 43 nM for A1R, A2R, and A3R receptors, respectively, in transfected CHO cells).{34118,27925} When microinjected into the rat brainstem, it increases blood pressure and heart rate.{34115} It is effective for pain in normal and nerve-injured rats and shows anticonvulsant activity in a rat model of generalized seizures.{34116,34117}  

     

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    SKU:21448 -

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  • N6-Ethyladenosine is an adenosine A1 and A3 receptor agonist.{48610} It binds selectively to rat adenosine A1 and human adenosine A3 receptors over rat adenosine A2A and A3 receptors (Kis = 4.9, 4.7, 8,900 and 1,050 nM, respectively, for the recombinant receptors in CHO cells). N6-Ethyladenosine completely inhibits forskolin-induced cAMP accumulation in CHO cells expressing the human recombinant adenosine A3 receptor when used at a concentration of 10 µM.  

     

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    SKU:28428 - 1 mg

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  • N6-Ethyladenosine is an adenosine A1 and A3 receptor agonist.{48610} It binds selectively to rat adenosine A1 and human adenosine A3 receptors over rat adenosine A2A and A3 receptors (Kis = 4.9, 4.7, 8,900 and 1,050 nM, respectively, for the recombinant receptors in CHO cells). N6-Ethyladenosine completely inhibits forskolin-induced cAMP accumulation in CHO cells expressing the human recombinant adenosine A3 receptor when used at a concentration of 10 µM.  

     

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    SKU:28428 - 10 mg

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  • N6-Ethyladenosine is an adenosine A1 and A3 receptor agonist.{48610} It binds selectively to rat adenosine A1 and human adenosine A3 receptors over rat adenosine A2A and A3 receptors (Kis = 4.9, 4.7, 8,900 and 1,050 nM, respectively, for the recombinant receptors in CHO cells). N6-Ethyladenosine completely inhibits forskolin-induced cAMP accumulation in CHO cells expressing the human recombinant adenosine A3 receptor when used at a concentration of 10 µM.  

     

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    SKU:28428 - 5 mg

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  • N6-Methyladenine is a modified purine that is commonly found in genomes of prokaryotes, protists, and plants.{29447,29365} It is less common in higher eukaryotes and extremely rare in mammals.{29447,29364} Like methylation of other DNA residues, N6-methyladenine represents an epigenetic modification that can affect diverse DNA functions, including replication, repair, and expression.{29447,29364}  

     

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  • N6-Methyladenine is a modified purine that is commonly found in genomes of prokaryotes, protists, and plants.{29447,29365} It is less common in higher eukaryotes and extremely rare in mammals.{29447,29364} Like methylation of other DNA residues, N6-methyladenine represents an epigenetic modification that can affect diverse DNA functions, including replication, repair, and expression.{29447,29364}  

     

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  • N6-Methyladenine is a modified purine that is commonly found in genomes of prokaryotes, protists, and plants.{29447,29365} It is less common in higher eukaryotes and extremely rare in mammals.{29447,29364} Like methylation of other DNA residues, N6-methyladenine represents an epigenetic modification that can affect diverse DNA functions, including replication, repair, and expression.{29447,29364}  

     

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  • N6-Methyladenine is a modified purine that is commonly found in genomes of prokaryotes, protists, and plants.{29447,29365} It is less common in higher eukaryotes and extremely rare in mammals.{29447,29364} Like methylation of other DNA residues, N6-methyladenine represents an epigenetic modification that can affect diverse DNA functions, including replication, repair, and expression.{29447,29364}  

     

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  • N6-Methyladenosine is an adenosine analog.{48666} It inhibits epinephrine-induced contraction of isolated guinea pig ileum and thoracic aorta when used at a concentration of 10 μM. N6-Methyladenosine (1 mg/kg, i.v.) decreases arterial blood pressure and renal blood flow and increases peripheral resistance in anesthetized dogs.{48667} It also inhibits tumor growth in the C3H/ST and C3HB/ST mouse models of spontaneous mammary adenocarcinomas.{48668} N6-Methyladenosine is also the most prevelant mRNA modification in eukaryotes and has roles in cell viability and development.{35631}  

     

    Brand:
    Cayman
    SKU:28833 - 1 g

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  • N6-Methyladenosine is an adenosine analog.{48666} It inhibits epinephrine-induced contraction of isolated guinea pig ileum and thoracic aorta when used at a concentration of 10 μM. N6-Methyladenosine (1 mg/kg, i.v.) decreases arterial blood pressure and renal blood flow and increases peripheral resistance in anesthetized dogs.{48667} It also inhibits tumor growth in the C3H/ST and C3HB/ST mouse models of spontaneous mammary adenocarcinomas.{48668} N6-Methyladenosine is also the most prevelant mRNA modification in eukaryotes and has roles in cell viability and development.{35631}  

     

    Brand:
    Cayman
    SKU:28833 - 250 mg

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  • N6-Methyladenosine is an adenosine analog.{48666} It inhibits epinephrine-induced contraction of isolated guinea pig ileum and thoracic aorta when used at a concentration of 10 μM. N6-Methyladenosine (1 mg/kg, i.v.) decreases arterial blood pressure and renal blood flow and increases peripheral resistance in anesthetized dogs.{48667} It also inhibits tumor growth in the C3H/ST and C3HB/ST mouse models of spontaneous mammary adenocarcinomas.{48668} N6-Methyladenosine is also the most prevelant mRNA modification in eukaryotes and has roles in cell viability and development.{35631}  

     

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    Cayman
    SKU:28833 - 500 mg

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  • N6-Methyladenosine 5′-monophosphate is an activator of glycogen phosphorylase b (Ka = 22 µM).{36175} It is also a non-competitive inhibitor of rat adenylate kinase II (Ki = 4.2 mM).{36174} N6-Methyladenosine 5’-monophosphate (sodium salt) has been used for immunoprecipitation of N6-methyladenosine.{36173}  

     

    Brand:
    Cayman
    SKU:23382 - 10 mg

    Available on backorder

  • N6-Methyladenosine 5′-monophosphate is an activator of glycogen phosphorylase b (Ka = 22 µM).{36175} It is also a non-competitive inhibitor of rat adenylate kinase II (Ki = 4.2 mM).{36174} N6-Methyladenosine 5’-monophosphate (sodium salt) has been used for immunoprecipitation of N6-methyladenosine.{36173}  

     

    Brand:
    Cayman
    SKU:23382 - 25 mg

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  • N6-Methyladenosine 5′-monophosphate is an activator of glycogen phosphorylase b (Ka = 22 µM).{36175} It is also a non-competitive inhibitor of rat adenylate kinase II (Ki = 4.2 mM).{36174} N6-Methyladenosine 5’-monophosphate (sodium salt) has been used for immunoprecipitation of N6-methyladenosine.{36173}  

     

    Brand:
    Cayman
    SKU:23382 - 5 mg

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  • N6022 is a tight-binding, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR; IC50 = 8 nM; Ki = 2.5 nM).{33360} It is reported to bind in the GSNO substrate binding pocket like a competitive inhibitor, although in kinetic assays it behaves with a mixed uncompetitive mode of inhibition toward the GSNO substrate and a mixed competitive mode of inhibition toward the formaldehyde adduct, S-hydroxymethylglutathione.{33360}  

     

    Brand:
    Cayman
    SKU:21269 -

    Out of stock

  • N6022 is a tight-binding, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR; IC50 = 8 nM; Ki = 2.5 nM).{33360} It is reported to bind in the GSNO substrate binding pocket like a competitive inhibitor, although in kinetic assays it behaves with a mixed uncompetitive mode of inhibition toward the GSNO substrate and a mixed competitive mode of inhibition toward the formaldehyde adduct, S-hydroxymethylglutathione.{33360}  

     

    Brand:
    Cayman
    SKU:21269 -

    Out of stock

  • N6022 is a tight-binding, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR; IC50 = 8 nM; Ki = 2.5 nM).{33360} It is reported to bind in the GSNO substrate binding pocket like a competitive inhibitor, although in kinetic assays it behaves with a mixed uncompetitive mode of inhibition toward the GSNO substrate and a mixed competitive mode of inhibition toward the formaldehyde adduct, S-hydroxymethylglutathione.{33360}  

     

    Brand:
    Cayman
    SKU:21269 -

    Out of stock

  • N6022 is a tight-binding, specific, and fully reversible inhibitor of S-nitrosoglutathione reductase (GSNOR; IC50 = 8 nM; Ki = 2.5 nM).{33360} It is reported to bind in the GSNO substrate binding pocket like a competitive inhibitor, although in kinetic assays it behaves with a mixed uncompetitive mode of inhibition toward the GSNO substrate and a mixed competitive mode of inhibition toward the formaldehyde adduct, S-hydroxymethylglutathione.{33360}  

     

    Brand:
    Cayman
    SKU:21269 -

    Out of stock

  • NAB 2 is an inhibitor of α-synuclein-induced toxicity.{46118} It prevents α-synuclein-induced defects in Rsp5-dependent endocytosis and vacuolar delivery of Mup1, Golgi-to-vacuole trafficking of Sna3, and degradation of Bap2 in wild-type yeast cells. NAB 2 also prevents formation of α-synuclein foci in wild-type yeast cells, an effect that is prevented by the rsp5G747E point mutation.  

     

    Brand:
    Cayman
    SKU:26145 - 1 mg

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  • NAB 2 is an inhibitor of α-synuclein-induced toxicity.{46118} It prevents α-synuclein-induced defects in Rsp5-dependent endocytosis and vacuolar delivery of Mup1, Golgi-to-vacuole trafficking of Sna3, and degradation of Bap2 in wild-type yeast cells. NAB 2 also prevents formation of α-synuclein foci in wild-type yeast cells, an effect that is prevented by the rsp5G747E point mutation.  

     

    Brand:
    Cayman
    SKU:26145 - 10 mg

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  • NAB 2 is an inhibitor of α-synuclein-induced toxicity.{46118} It prevents α-synuclein-induced defects in Rsp5-dependent endocytosis and vacuolar delivery of Mup1, Golgi-to-vacuole trafficking of Sna3, and degradation of Bap2 in wild-type yeast cells. NAB 2 also prevents formation of α-synuclein foci in wild-type yeast cells, an effect that is prevented by the rsp5G747E point mutation.  

     

    Brand:
    Cayman
    SKU:26145 - 5 mg

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  • Nabumetone is a non-steroidal anti-inflammatory drug (NSAID) and a prodrug form of 6-methoxy naphthalene acetic acid (Item No. 70620).{32442} Nabumetone (5-45 mg/kg) reduces carrageenan-induced edema in rats, as well as UV-induced erythema in guinea pigs (ED50 = 11 mg/kg).{32441} It reduces phenyl-p-quinone-induced writhing in mice (ED50 = 152 mg/kg). Nabumetone (50, 100, and 200 mg/kg) reduces endotoxin-induced pyresis in rabbits.  

     

    Brand:
    Cayman
    SKU:20251 -

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  • Nabumetone is a non-steroidal anti-inflammatory drug (NSAID) and a prodrug form of 6-methoxy naphthalene acetic acid (Item No. 70620).{32442} Nabumetone (5-45 mg/kg) reduces carrageenan-induced edema in rats, as well as UV-induced erythema in guinea pigs (ED50 = 11 mg/kg).{32441} It reduces phenyl-p-quinone-induced writhing in mice (ED50 = 152 mg/kg). Nabumetone (50, 100, and 200 mg/kg) reduces endotoxin-induced pyresis in rabbits.  

     

    Brand:
    Cayman
    SKU:20251 -

    Available on backorder

  • Nabumetone is a non-steroidal anti-inflammatory drug (NSAID) and a prodrug form of 6-methoxy naphthalene acetic acid (Item No. 70620).{32442} Nabumetone (5-45 mg/kg) reduces carrageenan-induced edema in rats, as well as UV-induced erythema in guinea pigs (ED50 = 11 mg/kg).{32441} It reduces phenyl-p-quinone-induced writhing in mice (ED50 = 152 mg/kg). Nabumetone (50, 100, and 200 mg/kg) reduces endotoxin-induced pyresis in rabbits.  

     

    Brand:
    Cayman
    SKU:20251 -

    Available on backorder

  • Nabumetone is a non-steroidal anti-inflammatory drug (NSAID) and a prodrug form of 6-methoxy naphthalene acetic acid (Item No. 70620).{32442} Nabumetone (5-45 mg/kg) reduces carrageenan-induced edema in rats, as well as UV-induced erythema in guinea pigs (ED50 = 11 mg/kg).{32441} It reduces phenyl-p-quinone-induced writhing in mice (ED50 = 152 mg/kg). Nabumetone (50, 100, and 200 mg/kg) reduces endotoxin-induced pyresis in rabbits.  

     

    Brand:
    Cayman
    SKU:20251 -

    Available on backorder

  • Nabumetone-d3 is intended for use as an internal standard for the quantification of nabumetone (Item No. 20251) by GC- or LC-MS. Nabumetone is a non-steroidal anti-inflammatory drug (NSAID) and a prodrug form of 6-methoxy naphthalene acetic acid (Item No. 70620).{32442} Nabumetone (5-45 mg/kg) reduces carrageenan-induced edema in rats, as well as UV-induced erythema in guinea pigs (ED50 = 11 mg/kg).{32441} It reduces phenyl-p-quinone-induced writhing in mice (ED50 = 152 mg/kg). Nabumetone (50, 100, and 200 mg/kg) reduces endotoxin-induced pyresis in rabbits.  

     

    Brand:
    Cayman
    SKU:30721 - 1 mg

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  • NAD+, known more formally as nicotinamide adenine dinucleotide, is a signaling molecule as well as a cofactor or substrate for many enzymes.{20368} It acts as an oxidizing agent, accepting electrons from other molecules while being converted to its reduced form, NADH (Item No. 16078).{20368} NAD+ is also essential for the activity of several enzymes, including poly(ADP)-ribose polymerases and cADP-ribose synthases.{20368} For example, it is used by some sirtuins to mediate protein deacetylation, producing O-acetyl-ADP-ribose and nicotinamide as well as the deacetylated protein.{16292}  

     

    Brand:
    Cayman
    SKU:-
  • NAD+, known more formally as nicotinamide adenine dinucleotide, is a signaling molecule as well as a cofactor or substrate for many enzymes.{20368} It acts as an oxidizing agent, accepting electrons from other molecules while being converted to its reduced form, NADH (Item No. 16078).{20368} NAD+ is also essential for the activity of several enzymes, including poly(ADP)-ribose polymerases and cADP-ribose synthases.{20368} For example, it is used by some sirtuins to mediate protein deacetylation, producing O-acetyl-ADP-ribose and nicotinamide as well as the deacetylated protein.{16292}  

     

    Brand:
    Cayman
    SKU:-
  • NAD+, known more formally as nicotinamide adenine dinucleotide, is a signaling molecule as well as a cofactor or substrate for many enzymes.{20368} It acts as an oxidizing agent, accepting electrons from other molecules while being converted to its reduced form, NADH (Item No. 16078).{20368} NAD+ is also essential for the activity of several enzymes, including poly(ADP)-ribose polymerases and cADP-ribose synthases.{20368} For example, it is used by some sirtuins to mediate protein deacetylation, producing O-acetyl-ADP-ribose and nicotinamide as well as the deacetylated protein.{16292}  

     

    Brand:
    Cayman
    SKU:-
  • NADH is the reduced form of nicotinamide adenine dinucleotide (NAD) that can donate electrons as part of a reducing reaction. In that process, NADH becomes oxidized to produce NAD+ (Item No. 16077). A variety of enzymes use NADH plus H+ to reduce substrates, generating NAD+ as well as the reduced product.{24341,9247,24936} For example, NADH:ubiquinone oxidoreductase accepts two electrons from NADH and passes them to ubiquinone (coenzyme Q) as part of the mitochondrial electron transport chain.{24936}  

     

    Brand:
    Cayman
    SKU:-
  • NADH is the reduced form of nicotinamide adenine dinucleotide (NAD) that can donate electrons as part of a reducing reaction. In that process, NADH becomes oxidized to produce NAD+ (Item No. 16077). A variety of enzymes use NADH plus H+ to reduce substrates, generating NAD+ as well as the reduced product.{24341,9247,24936} For example, NADH:ubiquinone oxidoreductase accepts two electrons from NADH and passes them to ubiquinone (coenzyme Q) as part of the mitochondrial electron transport chain.{24936}  

     

    Brand:
    Cayman
    SKU:-
  • NADH is the reduced form of nicotinamide adenine dinucleotide (NAD) that can donate electrons as part of a reducing reaction. In that process, NADH becomes oxidized to produce NAD+ (Item No. 16077). A variety of enzymes use NADH plus H+ to reduce substrates, generating NAD+ as well as the reduced product.{24341,9247,24936} For example, NADH:ubiquinone oxidoreductase accepts two electrons from NADH and passes them to ubiquinone (coenzyme Q) as part of the mitochondrial electron transport chain.{24936}  

     

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    Cayman
    SKU:-
  • Nadifloxacin is a fluoroquinolone antibiotic that is used topically. It is effective against the Gram-positive bacteria S. aureus and P. acnes, as well as Gram-negative bacteria.{27493,32024,32025}  

     

    Brand:
    Cayman
    SKU:20252 -

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  • Nadifloxacin is a fluoroquinolone antibiotic that is used topically. It is effective against the Gram-positive bacteria S. aureus and P. acnes, as well as Gram-negative bacteria.{27493,32024,32025}  

     

    Brand:
    Cayman
    SKU:20252 -

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  • Nadifloxacin is a fluoroquinolone antibiotic that is used topically. It is effective against the Gram-positive bacteria S. aureus and P. acnes, as well as Gram-negative bacteria.{27493,32024,32025}  

     

    Brand:
    Cayman
    SKU:20252 -

    Available on backorder

  • Nadifloxacin is a fluoroquinolone antibiotic that is used topically. It is effective against the Gram-positive bacteria S. aureus and P. acnes, as well as Gram-negative bacteria.{27493,32024,32025}  

     

    Brand:
    Cayman
    SKU:20252 -

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  • NADP+ is the oxidized form of the electron donor nicotinamide adenine dinucleotide phosphate (NADPH, Item No. 9000743). It serves as a cofactor in various biological reactions.{26206,26203} In addition, the balance between these reduced and oxidized forms plays key roles in diverse cellular functions, including cell survival, the maintenance of redox status, and intracellular signaling.{26203,26205} For example, binding of NADP+ to β-subunits of Kv channels activates ion transport, whereas NADPH stabilizes channel inactivation.{26202} NADP+ is biosynthesized from NAD+ (Item No. 16077) by NAD kinase, with ATP as the phosphoryl donor.{26204}  

     

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    Cayman
    SKU:10004675 - 1 g

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  • NADP+ is the oxidized form of the electron donor nicotinamide adenine dinucleotide phosphate (NADPH, Item No. 9000743). It serves as a cofactor in various biological reactions.{26206,26203} In addition, the balance between these reduced and oxidized forms plays key roles in diverse cellular functions, including cell survival, the maintenance of redox status, and intracellular signaling.{26203,26205} For example, binding of NADP+ to β-subunits of Kv channels activates ion transport, whereas NADPH stabilizes channel inactivation.{26202} NADP+ is biosynthesized from NAD+ (Item No. 16077) by NAD kinase, with ATP as the phosphoryl donor.{26204}  

     

    Brand:
    Cayman
    SKU:10004675 - 100 mg

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  • NADP+ is the oxidized form of the electron donor nicotinamide adenine dinucleotide phosphate (NADPH, Item No. 9000743). It serves as a cofactor in various biological reactions.{26206,26203} In addition, the balance between these reduced and oxidized forms plays key roles in diverse cellular functions, including cell survival, the maintenance of redox status, and intracellular signaling.{26203,26205} For example, binding of NADP+ to β-subunits of Kv channels activates ion transport, whereas NADPH stabilizes channel inactivation.{26202} NADP+ is biosynthesized from NAD+ (Item No. 16077) by NAD kinase, with ATP as the phosphoryl donor.{26204}  

     

    Brand:
    Cayman
    SKU:10004675 - 250 mg

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  • NADP+ is the oxidized form of the electron donor nicotinamide adenine dinucleotide phosphate (NADPH, Item No. 9000743). It serves as a cofactor in various biological reactions.{26206,26203} In addition, the balance between these reduced and oxidized forms plays key roles in diverse cellular functions, including cell survival, the maintenance of redox status, and intracellular signaling.{26203,26205} For example, binding of NADP+ to β-subunits of Kv channels activates ion transport, whereas NADPH stabilizes channel inactivation.{26202} NADP+ is biosynthesized from NAD+ (Item No. 16077) by NAD kinase, with ATP as the phosphoryl donor.{26204}  

     

    Brand:
    Cayman
    SKU:10004675 - 50 mg

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  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals it is predominantly produced by the pentose phosphate pathway, but it is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:20945 -

    Out of stock

  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals it is predominantly produced by the pentose phosphate pathway, but it is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:20945 -

    Out of stock

  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals it is predominantly produced by the pentose phosphate pathway, but it is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:20945 -

    Out of stock

  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals it is predominantly produced by the pentose phosphate pathway, but it is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:20945 -

    Out of stock

  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals is it predominantly produced by the pentose phosphate pathway, but is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:9000743 - 100 mg

    Available on backorder

  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals is it predominantly produced by the pentose phosphate pathway, but is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:9000743 - 25 mg

    Available on backorder

  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals is it predominantly produced by the pentose phosphate pathway, but is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:9000743 - 250 mg

    Available on backorder

  • NADPH is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate (NADP+) and acts as an electron donor in various biological reactions. In plants, NADPH is produced by ferredoxin-NADP+ reductase in the last step of the electron chain during photosynthesis. In animals is it predominantly produced by the pentose phosphate pathway, but is also generated by key mitochondrial enzymes. NADPH provides the reducing equivalents for biosynthetic reactions and the oxidation-reduction involved in protecting against the toxicity of reactive oxygen species.{17018,2511,17024} It is also used for the synthesis of lipids and cholesterol and during the process of fatty acid chain elongation.{5994}  

     

    Brand:
    Cayman
    SKU:9000743 - 50 mg

    Available on backorder

  • Nafamostat is a serine protease inhibitor that is capable of inhibiting trypsin (a digestive system protease; Ki = 15 nM), tryptase (a mast cell protease; Ki = 95.3 pM), and additional proteases in the coagulation cascade including thrombin (Ki = 0.84 μM).{23663} In a mouse model of allergic asthma, a dose of 300 mg/kg nafamostat mesylate has been shown to inhibit serine proteolytic activity, to decrease circulating levels of eosinophils and lymphocytes in bronchoalveolar lavage fluid, and to reduce interleukin-13 and eotaxin production associated with antigen-induced airway eosinophilia and goblet cell hyperplasia.{23662}  

     

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    Cayman
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  • Nafamostat is a serine protease inhibitor that is capable of inhibiting trypsin (a digestive system protease; Ki = 15 nM), tryptase (a mast cell protease; Ki = 95.3 pM), and additional proteases in the coagulation cascade including thrombin (Ki = 0.84 μM).{23663} In a mouse model of allergic asthma, a dose of 300 mg/kg nafamostat mesylate has been shown to inhibit serine proteolytic activity, to decrease circulating levels of eosinophils and lymphocytes in bronchoalveolar lavage fluid, and to reduce interleukin-13 and eotaxin production associated with antigen-induced airway eosinophilia and goblet cell hyperplasia.{23662}  

     

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    Cayman
    SKU:-
  • Nafamostat is a serine protease inhibitor that is capable of inhibiting trypsin (a digestive system protease; Ki = 15 nM), tryptase (a mast cell protease; Ki = 95.3 pM), and additional proteases in the coagulation cascade including thrombin (Ki = 0.84 μM).{23663} In a mouse model of allergic asthma, a dose of 300 mg/kg nafamostat mesylate has been shown to inhibit serine proteolytic activity, to decrease circulating levels of eosinophils and lymphocytes in bronchoalveolar lavage fluid, and to reduce interleukin-13 and eotaxin production associated with antigen-induced airway eosinophilia and goblet cell hyperplasia.{23662}  

     

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    Cayman
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  • Nafarelin is an agonist of gonadotropin-releasing hormone (GNRH).{40488,40489,40490} It is a long-acting agent that, after an initial increase in sex hormone levels, decreases the level of circulating gonadotropins and sex hormones. In vivo, nafarelin (0.5-2.0 μg/kg, s.c.) reduces plasma levels of luteinizing hormone and testosterone (Item Nos. 15645 | ISO60154) as well as testicular volume, sperm count, sperm motility, and duration of ejaculation in male dogs.{40488} Nafarelin (32 μg/animal per day) inhibits estrus in female beagle dogs.{40489} It also reduces the volume of endometrial tissue in a rat model of endometriosis.{40490} Formulations containing nafarelin have been used in the treatment of endometriosis and central precocious puberty.  

     

    Brand:
    Cayman
    SKU:24070 - 1 mg

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  • Nafarelin is an agonist of gonadotropin-releasing hormone (GNRH).{40488,40489,40490} It is a long-acting agent that, after an initial increase in sex hormone levels, decreases the level of circulating gonadotropins and sex hormones. In vivo, nafarelin (0.5-2.0 μg/kg, s.c.) reduces plasma levels of luteinizing hormone and testosterone (Item Nos. 15645 | ISO60154) as well as testicular volume, sperm count, sperm motility, and duration of ejaculation in male dogs.{40488} Nafarelin (32 μg/animal per day) inhibits estrus in female beagle dogs.{40489} It also reduces the volume of endometrial tissue in a rat model of endometriosis.{40490} Formulations containing nafarelin have been used in the treatment of endometriosis and central precocious puberty.  

     

    Brand:
    Cayman
    SKU:24070 - 10 mg

    Available on backorder

  • Nafarelin is an agonist of gonadotropin-releasing hormone (GNRH).{40488,40489,40490} It is a long-acting agent that, after an initial increase in sex hormone levels, decreases the level of circulating gonadotropins and sex hormones. In vivo, nafarelin (0.5-2.0 μg/kg, s.c.) reduces plasma levels of luteinizing hormone and testosterone (Item Nos. 15645 | ISO60154) as well as testicular volume, sperm count, sperm motility, and duration of ejaculation in male dogs.{40488} Nafarelin (32 μg/animal per day) inhibits estrus in female beagle dogs.{40489} It also reduces the volume of endometrial tissue in a rat model of endometriosis.{40490} Formulations containing nafarelin have been used in the treatment of endometriosis and central precocious puberty.  

     

    Brand:
    Cayman
    SKU:24070 - 5 mg

    Available on backorder

  • Nafarelin is an agonist of gonadotropin-releasing hormone (GNRH).{40488,40489,40490} It is a long-acting agent that, after an initial increase in sex hormone levels, decreases the level of circulating gonadotropins and sex hormones. In vivo, nafarelin (0.5-2.0 μg/kg, s.c.) reduces plasma levels of luteinizing hormone and testosterone (Item Nos. 15645 | ISO60154) as well as testicular volume, sperm count, sperm motility, and duration of ejaculation in male dogs.{40488} Nafarelin (32 μg/animal per day) inhibits estrus in female beagle dogs.{40489} It also reduces the volume of endometrial tissue in a rat model of endometriosis.{40490} Formulations containing nafarelin have been used in the treatment of endometriosis and central precocious puberty.  

     

    Brand:
    Cayman
    SKU:24070 - 500 µg

    Available on backorder

  • Nafcillin is a semisynthetic β-lactam antibiotic that shows resistance to staphylococcal penicillinase.{32140} Nafcillin is particularly effective against methicillin-sensitive strains of S. aureus, as shown in animal models and clinical trials.{32974,32975}  

     

    Brand:
    Cayman
    SKU:21008 -

    Out of stock

  • Nafcillin is a semisynthetic β-lactam antibiotic that shows resistance to staphylococcal penicillinase.{32140} Nafcillin is particularly effective against methicillin-sensitive strains of S. aureus, as shown in animal models and clinical trials.{32974,32975}  

     

    Brand:
    Cayman
    SKU:21008 -

    Out of stock

  • Nafcillin is a semisynthetic β-lactam antibiotic that shows resistance to staphylococcal penicillinase.{32140} Nafcillin is particularly effective against methicillin-sensitive strains of S. aureus, as shown in animal models and clinical trials.{32974,32975}  

     

    Brand:
    Cayman
    SKU:21008 -

    Out of stock

  • Nafcillin is a semisynthetic β-lactam antibiotic that shows resistance to staphylococcal penicillinase.{32140} Nafcillin is particularly effective against methicillin-sensitive strains of S. aureus, as shown in animal models and clinical trials.{32974,32975}  

     

    Brand:
    Cayman
    SKU:21008 -

    Out of stock

  • Naftifine is an allylamine compound that blocks ergosterol biosynthesis in fungi by inhibiting squalene epoxidase (Ki = 1.1 µM for C. albicans epoxidase).{17902}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Naftifine is an allylamine compound that blocks ergosterol biosynthesis in fungi by inhibiting squalene epoxidase (Ki = 1.1 µM for C. albicans epoxidase).{17902}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Naftifine is an allylamine compound that blocks ergosterol biosynthesis in fungi by inhibiting squalene epoxidase (Ki = 1.1 µM for C. albicans epoxidase).{17902}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Naftifine is an allylamine compound that blocks ergosterol biosynthesis in fungi by inhibiting squalene epoxidase (Ki = 1.1 µM for C. albicans epoxidase).{17902}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Naftifine-d3 is intended for use as an internal standard for the quantification of naftifine (Item No. 19234) by GC- or LC-MS. Naftifine is an allylamine compound that blocks ergosterol biosynthesis in fungi by inhibiting squalene epoxidase (Ki = 1.1 µM for C. albicans epoxidase).{17902}  

     

    Brand:
    Cayman
    SKU:29413 - 1 mg

    Available on backorder

  • Naftopidil is an α1-adrenergic receptor antagonist that competitively inhibits α-adrenoceptor-mediated contractions induced by noradrenaline with pA2 values of 6.73-8.15 in various blood vessels from dog, rabbit, guinea pig, and rat.{33266} It binds to the cloned human α1-adrenergic receptors with Ki values of 3.7, 20, and 1.2 nM for α1A, α1B and α1D, respectively.{33264} Clinical formulations of naftopidil are used in the treatment of benign prostatic hyperplasia in Japan.{33264} Naftopidil also exhibits antiproliferative activity, inhibiting the growth of androgen-sensitive LNcaP cells and androgen-insensitive PC-3 cancer cell lines with IC50 values of 22.2 and 33.2 µM, respectively.{33265}  

     

    Brand:
    Cayman
    SKU:21122 -

    Out of stock

  • Naftopidil is an α1-adrenergic receptor antagonist that competitively inhibits α-adrenoceptor-mediated contractions induced by noradrenaline with pA2 values of 6.73-8.15 in various blood vessels from dog, rabbit, guinea pig, and rat.{33266} It binds to the cloned human α1-adrenergic receptors with Ki values of 3.7, 20, and 1.2 nM for α1A, α1B and α1D, respectively.{33264} Clinical formulations of naftopidil are used in the treatment of benign prostatic hyperplasia in Japan.{33264} Naftopidil also exhibits antiproliferative activity, inhibiting the growth of androgen-sensitive LNcaP cells and androgen-insensitive PC-3 cancer cell lines with IC50 values of 22.2 and 33.2 µM, respectively.{33265}  

     

    Brand:
    Cayman
    SKU:21122 -

    Out of stock

  • Naftopidil is an α1-adrenergic receptor antagonist that competitively inhibits α-adrenoceptor-mediated contractions induced by noradrenaline with pA2 values of 6.73-8.15 in various blood vessels from dog, rabbit, guinea pig, and rat.{33266} It binds to the cloned human α1-adrenergic receptors with Ki values of 3.7, 20, and 1.2 nM for α1A, α1B and α1D, respectively.{33264} Clinical formulations of naftopidil are used in the treatment of benign prostatic hyperplasia in Japan.{33264} Naftopidil also exhibits antiproliferative activity, inhibiting the growth of androgen-sensitive LNcaP cells and androgen-insensitive PC-3 cancer cell lines with IC50 values of 22.2 and 33.2 µM, respectively.{33265}  

     

    Brand:
    Cayman
    SKU:21122 -

    Out of stock

  • Naftopidil is an α1-adrenergic receptor antagonist that competitively inhibits α-adrenoceptor-mediated contractions induced by noradrenaline with pA2 values of 6.73-8.15 in various blood vessels from dog, rabbit, guinea pig, and rat.{33266} It binds to the cloned human α1-adrenergic receptors with Ki values of 3.7, 20, and 1.2 nM for α1A, α1B and α1D, respectively.{33264} Clinical formulations of naftopidil are used in the treatment of benign prostatic hyperplasia in Japan.{33264} Naftopidil also exhibits antiproliferative activity, inhibiting the growth of androgen-sensitive LNcaP cells and androgen-insensitive PC-3 cancer cell lines with IC50 values of 22.2 and 33.2 µM, respectively.{33265}  

     

    Brand:
    Cayman
    SKU:21122 -

    Out of stock

  • Nalanthalide is a diterpenoid pyrone fungal metabolite that has been found in Nalanthamala and has potassium channel inhibitory and antiviral activities.{53575} It inhibits binding of the potassium channel inhibitor charybdotoxin (Item No. 24115) to Jurkat cell membranes (IC50 = 3 µM) and inhibits rubidium efflux from CHO cells expressing the voltage-gated potassium (Kv) channel Kv1.3 (IC50 = 3.9 µM). Nalanthalide depolarizes T cells in vitro with an EC50 value of 500 nM. It also inhibits HIV-1 integrase activity with IC50 values of 10 and 25 µM in coupled and strand transfer assays, respectively.{37200}  

     

    Brand:
    Cayman
    SKU:29724 - 1 mg

    Available on backorder

  • Naldemedine is a peripherally acting opioid receptor antagonist (IC50s = 1.15, 1.11, and 1.5 nM for recombinant human μ-, δ-, and κ-opioid receptors, respectively).{48812,48813} It inhibits opioid-induced emesis and vomiting in ferrets and opioid-induced constipation in rats (ED50 = 0.03 mg/kg for both) without affecting the analgesic effect of morphine in the tail-flick test in rats.{48812} Naldemedine induces the opioid withdrawal symptoms of diarrhea and teeth chattering, but not jumping, in morphine-dependent rats when administered at doses of 1 and 3 mg/kg, respectively.{48813} Formulations containing naldemedine have been used in the treatment of opioid-induced constipation.  

     

    Brand:
    Cayman
    SKU:29570 - 500 µg

    Available on backorder

  • Naled is an organophosphate insecticide and acaricide that inhibits acetylcholinesterase (AChE) and butyrylcholinesterase (BChE).{43652} It reduces the number of A. sollicitans mosquitos by 97% after one hour when aerially applied at a concentration of 0.1 pounds per acre.{43653} Naled (125 ppm AI) induces 100 and 64% mortality of T. telarius adults and immature mites, respectively, in an immediate contact toxicity test but does not induce mortality in mite eggs.{43654} It is toxic to rats with an LD50 value of 250 mg/kg.{41952} Formulations containing naled have been used in the control of mosquitoes in public areas and of crop-damaging insects in agriculture.  

     

    Brand:
    Cayman
    SKU:25783 - 100 mg

    Available on backorder

  • Nalfurafine is a κ-opioid receptor (KOR) agonist (EC50 = 0.05 nM for human receptors expressed in CHO cell membranes).{49051} It is selective for κ-opioid over μ- and δ-opioid receptors (EC50s = 0.72 and 74.1 nM, respectively). Nalfurafine (≥30 μg/kg) reduces scratching behavior induced by chloroquine (CQ; Item No. 14194) in mice, as well as locomotor activity when administered at a dose of 100 μg/kg.{49053} In rats, nalfurafine (≥0.01 mg/kg) reduces intracranial self-stimulation, lactic acid-induced stretching behavior, and scratching behavior induced by intradermal administration of serotonin (5-HT; Item No. 14332).{49054} Nalfurafine is also an orexin 1 receptor (OX1R) antagonist (Ki = 250 nM).{49052}  

     

    Brand:
    Cayman
    SKU:23186 - 1 mg

    Available on backorder

  • Nalfurafine is a κ-opioid receptor (KOR) agonist (EC50 = 0.05 nM for human receptors expressed in CHO cell membranes).{49051} It is selective for κ-opioid over μ- and δ-opioid receptors (EC50s = 0.72 and 74.1 nM, respectively). Nalfurafine (≥30 μg/kg) reduces scratching behavior induced by chloroquine (CQ; Item No. 14194) in mice, as well as locomotor activity when administered at a dose of 100 μg/kg.{49053} In rats, nalfurafine (≥0.01 mg/kg) reduces intracranial self-stimulation, lactic acid-induced stretching behavior, and scratching behavior induced by intradermal administration of serotonin (5-HT; Item No. 14332).{49054} Nalfurafine is also an orexin 1 receptor (OX1R) antagonist (Ki = 250 nM).{49052}  

     

    Brand:
    Cayman
    SKU:23186 - 10 mg

    Available on backorder

  • Nalfurafine is a κ-opioid receptor (KOR) agonist (EC50 = 0.05 nM for human receptors expressed in CHO cell membranes).{49051} It is selective for κ-opioid over μ- and δ-opioid receptors (EC50s = 0.72 and 74.1 nM, respectively). Nalfurafine (≥30 μg/kg) reduces scratching behavior induced by chloroquine (CQ; Item No. 14194) in mice, as well as locomotor activity when administered at a dose of 100 μg/kg.{49053} In rats, nalfurafine (≥0.01 mg/kg) reduces intracranial self-stimulation, lactic acid-induced stretching behavior, and scratching behavior induced by intradermal administration of serotonin (5-HT; Item No. 14332).{49054} Nalfurafine is also an orexin 1 receptor (OX1R) antagonist (Ki = 250 nM).{49052}  

     

    Brand:
    Cayman
    SKU:23186 - 5 mg

    Available on backorder

  • Nalidixic acid was the first quinolone-based antibiotic.{41042} It inhibits DNA gyrase and topoisomerase IV activity in Gram-negative bacteria with originally reported minimal bacteriostatic concentrations of 0.5-50.0 µg/ml.{41041,41042} Formulations containing nalidixic acid were used for the treatment of urinary tract infections.{41043} However, derivatives of nalidixic acid, comprising second, third, and fourth generation quinolones, have improved antibacterial actions and fewer adverse effects, so it is no longer used clinically.  

     

    Brand:
    Cayman
    SKU:19807 -

    Available on backorder

  • Nalidixic acid was the first quinolone-based antibiotic.{41042} It inhibits DNA gyrase and topoisomerase IV activity in Gram-negative bacteria with originally reported minimal bacteriostatic concentrations of 0.5-50.0 µg/ml.{41041,41042} Formulations containing nalidixic acid were used for the treatment of urinary tract infections.{41043} However, derivatives of nalidixic acid, comprising second, third, and fourth generation quinolones, have improved antibacterial actions and fewer adverse effects, so it is no longer used clinically.  

     

    Brand:
    Cayman
    SKU:19807 -

    Available on backorder

  • Nalidixic acid was the first quinolone-based antibiotic.{41042} It inhibits DNA gyrase and topoisomerase IV activity in Gram-negative bacteria with originally reported minimal bacteriostatic concentrations of 0.5-50.0 µg/ml.{41041,41042} Formulations containing nalidixic acid were used for the treatment of urinary tract infections.{41043} However, derivatives of nalidixic acid, comprising second, third, and fourth generation quinolones, have improved antibacterial actions and fewer adverse effects, so it is no longer used clinically.  

     

    Brand:
    Cayman
    SKU:19807 -

    Available on backorder

  • Nalidixic acid was the first quinolone-based antibiotic.{41042} It inhibits DNA gyrase and topoisomerase IV activity in Gram-negative bacteria with originally reported minimal bacteriostatic concentrations of 0.5-50.0 µg/ml.{41041,41042} Formulations containing nalidixic acid were used for the treatment of urinary tract infections.{41043} However, derivatives of nalidixic acid, comprising second, third, and fourth generation quinolones, have improved antibacterial actions and fewer adverse effects, so it is no longer used clinically.  

     

    Brand:
    Cayman
    SKU:19807 -

    Available on backorder

  • Naloxegol is a peripherally acting antagonist of the μ-opioid receptor (Ki = 7.42 nM; pA2 = 7.95).{39588} It is selective for the μ-opioid receptor over the δ-opioid receptor (Ki = 866 nM). Naloxegol also acts as a partial agonist of κ-opioid receptors in vitro (EC50 = 47 nM for [35S]GTPγS binding) but lacks activity ex vivo at concentrations up to 10 μM. In vivo, naloxegol reverses morphine-induced decreases in gastrointestinal motility and analgesia in a hot-plate assay in rats (ED50s = 23.1 and 55.4 mg/kg, respectively), demonstrating a two-fold separation for peripheral versus CNS effects. Naloxegol also exhibits a brain uptake rate comparable to atenolol, a low-permeation standard with no brain uptake, in a rat brain perfusion model.  

     

    Brand:
    Cayman
    SKU:23731 - 10 mg

    Available on backorder

  • Naloxegol is a peripherally acting antagonist of the μ-opioid receptor (Ki = 7.42 nM; pA2 = 7.95).{39588} It is selective for the μ-opioid receptor over the δ-opioid receptor (Ki = 866 nM). Naloxegol also acts as a partial agonist of κ-opioid receptors in vitro (EC50 = 47 nM for [35S]GTPγS binding) but lacks activity ex vivo at concentrations up to 10 μM. In vivo, naloxegol reverses morphine-induced decreases in gastrointestinal motility and analgesia in a hot-plate assay in rats (ED50s = 23.1 and 55.4 mg/kg, respectively), demonstrating a two-fold separation for peripheral versus CNS effects. Naloxegol also exhibits a brain uptake rate comparable to atenolol, a low-permeation standard with no brain uptake, in a rat brain perfusion model.  

     

    Brand:
    Cayman
    SKU:23731 - 25 mg

    Available on backorder

  • Naloxegol is a peripherally acting antagonist of the μ-opioid receptor (Ki = 7.42 nM; pA2 = 7.95).{39588} It is selective for the μ-opioid receptor over the δ-opioid receptor (Ki = 866 nM). Naloxegol also acts as a partial agonist of κ-opioid receptors in vitro (EC50 = 47 nM for [35S]GTPγS binding) but lacks activity ex vivo at concentrations up to 10 μM. In vivo, naloxegol reverses morphine-induced decreases in gastrointestinal motility and analgesia in a hot-plate assay in rats (ED50s = 23.1 and 55.4 mg/kg, respectively), demonstrating a two-fold separation for peripheral versus CNS effects. Naloxegol also exhibits a brain uptake rate comparable to atenolol, a low-permeation standard with no brain uptake, in a rat brain perfusion model.  

     

    Brand:
    Cayman
    SKU:23731 - 5 mg

    Available on backorder

  • Naloxegol is a peripherally acting antagonist of the μ-opioid receptor (Ki = 7.42 nM; pA2 = 7.95).{39588} It is selective for the μ-opioid receptor over the δ-opioid receptor (Ki = 866 nM). Naloxegol also acts as a partial agonist of κ-opioid receptors in vitro (EC50 = 47 nM for [35S]GTPγS binding) but lacks activity ex vivo at concentrations up to 10 μM. In vivo, naloxegol reverses morphine-induced decreases in gastrointestinal motility and analgesia in a hot-plate assay in rats (ED50s = 23.1 and 55.4 mg/kg, respectively), demonstrating a two-fold separation for peripheral versus CNS effects. Naloxegol also exhibits a brain uptake rate comparable to atenolol, a low-permeation standard with no brain uptake, in a rat brain perfusion model.  

     

    Brand:
    Cayman
    SKU:23731 - 50 mg

    Available on backorder

  • Naloxone (hydrochloride) (Item No. 15594) is an analytical reference standard categorized as an opioid antagonist.{25494} Formulations containing naloxone have been used as antidotes for opioid overdose and the prevention of overdose.{25491,25493} They have also been used in combination with buprenorphine (Item Nos. ISO60178 | 14025) in the treatment of opiate addiction and in pain management.{25495,25492} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • Naloxone (hydrochloride) (Item No. 15594) is an analytical reference standard categorized as an opioid antagonist.{25494} Formulations containing naloxone have been used as antidotes for opioid overdose and the prevention of overdose.{25491,25493} They have also been used in combination with buprenorphine (Item Nos. ISO60178 | 14025) in the treatment of opiate addiction and in pain management.{25495,25492} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • Naloxone (hydrochloride) (Item No. 15594) is an analytical reference standard categorized as an opioid antagonist.{25494} Formulations containing naloxone have been used as antidotes for opioid overdose and the prevention of overdose.{25491,25493} They have also been used in combination with buprenorphine (Item Nos. ISO60178 | 14025) in the treatment of opiate addiction and in pain management.{25495,25492} This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:-
  • Naltrindole is a potent antagonist of the human δ-opioid receptor (Ki = 0.02-0.3 nM), with much lower affinities for κ- and µ-opioid receptors (Kis = 10-66 and 6-64 nM, respectively).{9926,25533} Naltrindole is commonly used to investigate the role of the δ-opioid receptor in signaling responses to test compounds.{23792,23757,23935}  

     

    Brand:
    Cayman
    SKU:9000705 - 1 mg

    Available on backorder

  • Naltrindole is a potent antagonist of the human δ-opioid receptor (Ki = 0.02-0.3 nM), with much lower affinities for κ- and µ-opioid receptors (Kis = 10-66 and 6-64 nM, respectively).{9926,25533} Naltrindole is commonly used to investigate the role of the δ-opioid receptor in signaling responses to test compounds.{23792,23757,23935}  

     

    Brand:
    Cayman
    SKU:9000705 - 10 mg

    Available on backorder

  • Naltrindole is a potent antagonist of the human δ-opioid receptor (Ki = 0.02-0.3 nM), with much lower affinities for κ- and µ-opioid receptors (Kis = 10-66 and 6-64 nM, respectively).{9926,25533} Naltrindole is commonly used to investigate the role of the δ-opioid receptor in signaling responses to test compounds.{23792,23757,23935}  

     

    Brand:
    Cayman
    SKU:9000705 - 5 mg

    Available on backorder

  • NAMIE (Item No. 22631) is an analytical reference standard that is structurally similar to known synthetic cannabinoids. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:22631 -

    Out of stock

  • NAMIE (Item No. 22631) is an analytical reference standard that is structurally similar to known synthetic cannabinoids. This product is intended for research and forensic applications.  

     

    Brand:
    Cayman
    SKU:22631 -

    Out of stock

  • Nampt-IN-1 is a potent inhibitor of nicotinamide phosphoribosyltransferase (Nampt; IC50 = 3.1 nM).{36930} It is selective for Nampt over a panel of greater than 100 human kinases at 1 μM. Nampt-IN-1 inhibits NAD+ formation in and proliferation of HCT116 cells (IC50s = 1.8 and 8.9 nM, respectively). It inhibits cell growth in a panel of cancer cell lines (IC50s = + formation in an A2780 ovarian carcinoma mouse xenograft model (ED50 = 2 mg/kg).  

     

    Brand:
    Cayman
    SKU:26066 - 1 mg

    Available on backorder

  • Nampt-IN-1 is a potent inhibitor of nicotinamide phosphoribosyltransferase (Nampt; IC50 = 3.1 nM).{36930} It is selective for Nampt over a panel of greater than 100 human kinases at 1 μM. Nampt-IN-1 inhibits NAD+ formation in and proliferation of HCT116 cells (IC50s = 1.8 and 8.9 nM, respectively). It inhibits cell growth in a panel of cancer cell lines (IC50s = + formation in an A2780 ovarian carcinoma mouse xenograft model (ED50 = 2 mg/kg).  

     

    Brand:
    Cayman
    SKU:26066 - 10 mg

    Available on backorder

  • Nampt-IN-1 is a potent inhibitor of nicotinamide phosphoribosyltransferase (Nampt; IC50 = 3.1 nM).{36930} It is selective for Nampt over a panel of greater than 100 human kinases at 1 μM. Nampt-IN-1 inhibits NAD+ formation in and proliferation of HCT116 cells (IC50s = 1.8 and 8.9 nM, respectively). It inhibits cell growth in a panel of cancer cell lines (IC50s = + formation in an A2780 ovarian carcinoma mouse xenograft model (ED50 = 2 mg/kg).  

     

    Brand:
    Cayman
    SKU:26066 - 25 mg

    Available on backorder

  • Nampt-IN-1 is a potent inhibitor of nicotinamide phosphoribosyltransferase (Nampt; IC50 = 3.1 nM).{36930} It is selective for Nampt over a panel of greater than 100 human kinases at 1 μM. Nampt-IN-1 inhibits NAD+ formation in and proliferation of HCT116 cells (IC50s = 1.8 and 8.9 nM, respectively). It inhibits cell growth in a panel of cancer cell lines (IC50s = + formation in an A2780 ovarian carcinoma mouse xenograft model (ED50 = 2 mg/kg).  

     

    Brand:
    Cayman
    SKU:26066 - 5 mg

    Available on backorder

  • NAN-190 is a mixed antagonist and partial agonist of the serotonin (5-HT) receptor subtype 5-HT1A.{45661} It inhibits radioligand binding to 5-HT1A sites in rat hippocampal membranes (Ki = 2 nM). NAN-190 decreases 5-carboxamidotryptamine-mediated inhibition of forskolin-induced adenylyl cyclase activity in guinea pig hippocampal membranes in a concentration-dependent manner, indicating partial agonist activity. NAN-190 also antagonizes α1-adrenergic receptors (α1-ARs; pA2s = 9.47, 9.02, and 9.99 in isolated rat tail artery, rabbit aorta, and rat aorta, respectively).{45662} In vivo, NAN-190 (1-300 μg/kg) decreases blood pressure, without modifying heart rate, in anesthetized rats. It inhibits phenylephrine-induced pressor responses in pithed rats. NAN-190 (5 mg/kg, i.p.) potentiates the circadian response to light in dark-adapted and entrained hamsters.{45663}  

     

    Brand:
    Cayman
    SKU:29314 - 25 mg

    Available on backorder

  • NAN-190 is a mixed antagonist and partial agonist of the serotonin (5-HT) receptor subtype 5-HT1A.{45661} It inhibits radioligand binding to 5-HT1A sites in rat hippocampal membranes (Ki = 2 nM). NAN-190 decreases 5-carboxamidotryptamine-mediated inhibition of forskolin-induced adenylyl cyclase activity in guinea pig hippocampal membranes in a concentration-dependent manner, indicating partial agonist activity. NAN-190 also antagonizes α1-adrenergic receptors (α1-ARs; pA2s = 9.47, 9.02, and 9.99 in isolated rat tail artery, rabbit aorta, and rat aorta, respectively).{45662} In vivo, NAN-190 (1-300 μg/kg) decreases blood pressure, without modifying heart rate, in anesthetized rats. It inhibits phenylephrine-induced pressor responses in pithed rats. NAN-190 (5 mg/kg, i.p.) potentiates the circadian response to light in dark-adapted and entrained hamsters.{45663}  

     

    Brand:
    Cayman
    SKU:29314 - 50 mg

    Available on backorder

  • Nanaomycin A is a quinone bacterial metabolite originally isolated from Streptomyces that has antimicrobial activity.{45188} It inhibits the growth of a variety of bacteria (MICs = P. falciparum (IC80 = 0.033 µM).{45188,57310} Nanaomycin A is a selective DNA methyltransferase 3B (DNMT3B) inhibitor that inhibits proliferation of HCT116, A549, and HL-60 cancer cells (IC50s = 0.4, 4.1, and 0.8 µM, respectively).{57311} Nanaomycin A promotes the differentiation of human induced pluripotent stem (iPS) cells into hepatoblasts at the definitive endoderm cell-to-hepatoblast stage, but not the iPS cell-to-definitive endoderm cell stage, when used at a concentration of 1 µM.{57312}  

     

    Brand:
    Cayman
    SKU:9001479 - 5 mg

    Available on backorder

  • Nanchangmycin is a polyether ionophore antibiotic produced by S. nanchangensis NS3226 that has insecticidal and in vitro antibacterial properties.{34684},{34685} Nanchangmycin exhibits antiviral properties against Zika virus (ZIKV) by blocking viral entry in vitro in a spectrum of cell types, including U2OS, human microvascular endothelial cells, and placental Jeg3 cells (IC50s = 100, 400, and 970 nM, respectively).{34686} Nanchangmycin also blocks ZIKV entry into primary cells, including extravillous trophoblasts, human primary uterine microvascular endothelial cells, human umbilical vein endothelial cells, and murine primary midbrain neuron-glia cultures.{34686} Efficacy of nanchangmycin extends to other viruses where it blocks entry into U2OS cells by West Nile, dengue, Sindbis, and chikungunya viruses.{34686}  

     

    Brand:
    Cayman
    SKU:21679 -

    Out of stock

  • Nanchangmycin is a polyether ionophore antibiotic produced by S. nanchangensis NS3226 that has insecticidal and in vitro antibacterial properties.{34684},{34685} Nanchangmycin exhibits antiviral properties against Zika virus (ZIKV) by blocking viral entry in vitro in a spectrum of cell types, including U2OS, human microvascular endothelial cells, and placental Jeg3 cells (IC50s = 100, 400, and 970 nM, respectively).{34686} Nanchangmycin also blocks ZIKV entry into primary cells, including extravillous trophoblasts, human primary uterine microvascular endothelial cells, human umbilical vein endothelial cells, and murine primary midbrain neuron-glia cultures.{34686} Efficacy of nanchangmycin extends to other viruses where it blocks entry into U2OS cells by West Nile, dengue, Sindbis, and chikungunya viruses.{34686}  

     

    Brand:
    Cayman
    SKU:21679 -

    Out of stock

  • Nanchangmycin is a polyether ionophore antibiotic produced by S. nanchangensis NS3226 that has insecticidal and in vitro antibacterial properties.{34684},{34685} Nanchangmycin exhibits antiviral properties against Zika virus (ZIKV) by blocking viral entry in vitro in a spectrum of cell types, including U2OS, human microvascular endothelial cells, and placental Jeg3 cells (IC50s = 100, 400, and 970 nM, respectively).{34686} Nanchangmycin also blocks ZIKV entry into primary cells, including extravillous trophoblasts, human primary uterine microvascular endothelial cells, human umbilical vein endothelial cells, and murine primary midbrain neuron-glia cultures.{34686} Efficacy of nanchangmycin extends to other viruses where it blocks entry into U2OS cells by West Nile, dengue, Sindbis, and chikungunya viruses.{34686}  

     

    Brand:
    Cayman
    SKU:21679 -

    Out of stock

  • Nanchangmycin is a polyether ionophore antibiotic produced by S. nanchangensis NS3226 that has insecticidal and in vitro antibacterial properties.{34684},{34685} Nanchangmycin exhibits antiviral properties against Zika virus (ZIKV) by blocking viral entry in vitro in a spectrum of cell types, including U2OS, human microvascular endothelial cells, and placental Jeg3 cells (IC50s = 100, 400, and 970 nM, respectively).{34686} Nanchangmycin also blocks ZIKV entry into primary cells, including extravillous trophoblasts, human primary uterine microvascular endothelial cells, human umbilical vein endothelial cells, and murine primary midbrain neuron-glia cultures.{34686} Efficacy of nanchangmycin extends to other viruses where it blocks entry into U2OS cells by West Nile, dengue, Sindbis, and chikungunya viruses.{34686}  

     

    Brand:
    Cayman
    SKU:21679 -

    Out of stock

  • NAP 226-90 is a metabolite of rivastigmine (Item No. 14270) that is formed by hydrolysis.{46885}  

     

    Brand:
    Cayman
    SKU:30124 - 1 g

    Available on backorder

  • NAP 226-90 is a metabolite of rivastigmine (Item No. 14270) that is formed by hydrolysis.{46885}  

     

    Brand:
    Cayman
    SKU:30124 - 10 g

    Available on backorder

  • NAP 226-90 is a metabolite of rivastigmine (Item No. 14270) that is formed by hydrolysis.{46885}  

     

    Brand:
    Cayman
    SKU:30124 - 25 g

    Available on backorder