Chemicals

Showing 7201–7350 of 41137 results

  • 7-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine is a building block.{61033} It has been used in the synthesis of PI3K inhibitors.  

     

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    SKU:30944 - 1 mg

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  • 7-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine is a building block.{61033} It has been used in the synthesis of PI3K inhibitors.  

     

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    Cayman
    SKU:30944 - 10 mg

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  • 7-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine is a building block.{61033} It has been used in the synthesis of PI3K inhibitors.  

     

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    Cayman
    SKU:30944 - 25 mg

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  • 7-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine is a building block.{61033} It has been used in the synthesis of PI3K inhibitors.  

     

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    Cayman
    SKU:30944 - 5 mg

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  • 7-Methoxycoumarin is a coumarin that has been found in S. oblongifolia and has diverse biological activities.{57033,57034,57035} It reduces the release of prostaglandin E2 (PGE2; Item No. 14010) and leukotriene C4 (LTC4; Item No. 20210) induced by A23187 (Item No. 110160) in isolated mouse peritoneal macrophages.{57033} 7-Methyoxycoumarin is active against S. aureus, S. epidermidis, B. subtilis, S. lutea, and V. cholera (MICs = 0.5, 0.75, 0.75, 0.75, and 0.5 mg/ml, respectively).{57034} In vivo, 7-methoxycoumarin (3.5 and 7 mg/kg) reduces formalin-induced paw licking and biting responses in mice.{57035}  

     

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    Cayman
    SKU:30857 - 10 g

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  • 7-Methoxycoumarin is a coumarin that has been found in S. oblongifolia and has diverse biological activities.{57033,57034,57035} It reduces the release of prostaglandin E2 (PGE2; Item No. 14010) and leukotriene C4 (LTC4; Item No. 20210) induced by A23187 (Item No. 110160) in isolated mouse peritoneal macrophages.{57033} 7-Methyoxycoumarin is active against S. aureus, S. epidermidis, B. subtilis, S. lutea, and V. cholera (MICs = 0.5, 0.75, 0.75, 0.75, and 0.5 mg/ml, respectively).{57034} In vivo, 7-methoxycoumarin (3.5 and 7 mg/kg) reduces formalin-induced paw licking and biting responses in mice.{57035}  

     

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    Cayman
    SKU:30857 - 25 g

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  • 7-Methoxycoumarin is a coumarin that has been found in S. oblongifolia and has diverse biological activities.{57033,57034,57035} It reduces the release of prostaglandin E2 (PGE2; Item No. 14010) and leukotriene C4 (LTC4; Item No. 20210) induced by A23187 (Item No. 110160) in isolated mouse peritoneal macrophages.{57033} 7-Methyoxycoumarin is active against S. aureus, S. epidermidis, B. subtilis, S. lutea, and V. cholera (MICs = 0.5, 0.75, 0.75, 0.75, and 0.5 mg/ml, respectively).{57034} In vivo, 7-methoxycoumarin (3.5 and 7 mg/kg) reduces formalin-induced paw licking and biting responses in mice.{57035}  

     

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    Cayman
    SKU:30857 - 5 g

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  • 7-methyl-6-Thioguanosine is a chromophoric substrate that is used to quantify inorganic phosphate (Pi). In the presence of purine nucleoside phosphorylase, it reacts with Pi to produce 7-methyl-6-thioguanine and ribose 1-phosphate, with the increase in 7-methyl-6-thioguanine followed by continuous spectrophotometry at an absorbance of 355-360 nm.{26928} 7-methyl-6-Thioguanosine is also used to measure changes in Pi levels in coupled enzyme systems, including assays of the activities of protein phosphatases, phosphorylase kinases, GTPases, and ATPases.{26928,26932,26930,26931}  

     

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  • 7-methyl-6-Thioguanosine is a chromophoric substrate that is used to quantify inorganic phosphate (Pi). In the presence of purine nucleoside phosphorylase, it reacts with Pi to produce 7-methyl-6-thioguanine and ribose 1-phosphate, with the increase in 7-methyl-6-thioguanine followed by continuous spectrophotometry at an absorbance of 355-360 nm.{26928} 7-methyl-6-Thioguanosine is also used to measure changes in Pi levels in coupled enzyme systems, including assays of the activities of protein phosphatases, phosphorylase kinases, GTPases, and ATPases.{26928,26932,26930,26931}  

     

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    Cayman
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  • 7-methyl-6-Thioguanosine is a chromophoric substrate that is used to quantify inorganic phosphate (Pi). In the presence of purine nucleoside phosphorylase, it reacts with Pi to produce 7-methyl-6-thioguanine and ribose 1-phosphate, with the increase in 7-methyl-6-thioguanine followed by continuous spectrophotometry at an absorbance of 355-360 nm.{26928} 7-methyl-6-Thioguanosine is also used to measure changes in Pi levels in coupled enzyme systems, including assays of the activities of protein phosphatases, phosphorylase kinases, GTPases, and ATPases.{26928,26932,26930,26931}  

     

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  • 7-Methylguanine is a metabolite of the natural purine base whose N9 position is available for chemical modifications.{29474} This genotoxic adduct can be generated by DNA methylation and has been used as a probe of protein-DNA interactions and for DNA sequencing methods.{29476} It is also considered to be a carcinogenic biomarker for cigarette smoking that is detectable in urine.{29475}  

     

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  • 7-Methylguanine is a metabolite of the natural purine base whose N9 position is available for chemical modifications.{29474} This genotoxic adduct can be generated by DNA methylation and has been used as a probe of protein-DNA interactions and for DNA sequencing methods.{29476} It is also considered to be a carcinogenic biomarker for cigarette smoking that is detectable in urine.{29475}  

     

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  • 7-Methylguanine is a metabolite of the natural purine base whose N9 position is available for chemical modifications.{29474} This genotoxic adduct can be generated by DNA methylation and has been used as a probe of protein-DNA interactions and for DNA sequencing methods.{29476} It is also considered to be a carcinogenic biomarker for cigarette smoking that is detectable in urine.{29475}  

     

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  • 7-Methylguanine is a metabolite of the natural purine base whose N9 position is available for chemical modifications.{29474} This genotoxic adduct can be generated by DNA methylation and has been used as a probe of protein-DNA interactions and for DNA sequencing methods.{29476} It is also considered to be a carcinogenic biomarker for cigarette smoking that is detectable in urine.{29475}  

     

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  • 7-Methylguanosine is a purine base modified by the addition of a methyl group and closely resembles the 5’ terminal cap structure present on eukaryotic mRNA.{25956} It cannot be rephosphorylated and reused for de novo synthesis, and so is excreted by cells and can be detected in serum and urine. It has been used as a biomarker for some types of cancer.{17048}  

     

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  • 7-Methylguanosine is a purine base modified by the addition of a methyl group and closely resembles the 5’ terminal cap structure present on eukaryotic mRNA.{25956} It cannot be rephosphorylated and reused for de novo synthesis, and so is excreted by cells and can be detected in serum and urine. It has been used as a biomarker for some types of cancer.{17048}  

     

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  • 7-Methylguanosine is a purine base modified by the addition of a methyl group and closely resembles the 5’ terminal cap structure present on eukaryotic mRNA.{25956} It cannot be rephosphorylated and reused for de novo synthesis, and so is excreted by cells and can be detected in serum and urine. It has been used as a biomarker for some types of cancer.{17048}  

     

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    Cayman
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  • 7-Methylguanosine is a purine base modified by the addition of a methyl group and closely resembles the 5’ terminal cap structure present on eukaryotic mRNA.{25956} It cannot be rephosphorylated and reused for de novo synthesis, and so is excreted by cells and can be detected in serum and urine. It has been used as a biomarker for some types of cancer.{17048}  

     

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  • 7-Methyluric acid is a methylated purine and uric acid (Item No. 16219) derivative. It is a metabolite of caffeine (Item No. 14118) that can be detected in urine.{33335,31341} 7-Methyluric acid can also be detected in uric acid stones.{33336}  

     

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    Cayman
    SKU:21067 -

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  • 7-Methyluric acid is a methylated purine and uric acid (Item No. 16219) derivative. It is a metabolite of caffeine (Item No. 14118) that can be detected in urine.{33335,31341} 7-Methyluric acid can also be detected in uric acid stones.{33336}  

     

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    Cayman
    SKU:21067 -

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  • 7-Methyluric acid is a methylated purine and uric acid (Item No. 16219) derivative. It is a metabolite of caffeine (Item No. 14118) that can be detected in urine.{33335,31341} 7-Methyluric acid can also be detected in uric acid stones.{33336}  

     

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    Cayman
    SKU:21067 -

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  • 7-Nitroindazole is a non-selective inhibitor of NOS isoforms in vitro. However, it shows good anti-nociceptive effects in vivo without affecting blood pressure via inhibition of eNOS.{1220} The IC50 values for inhibition of rat nNOS, bovine eNOS, and rat iNOS are 0.71, 0.78, and 5.8 µM, respectively.{1339}  

     

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    Cayman
    SKU:81340 - 100 mg

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  • 7-Nitroindazole is a non-selective inhibitor of NOS isoforms in vitro. However, it shows good anti-nociceptive effects in vivo without affecting blood pressure via inhibition of eNOS.{1220} The IC50 values for inhibition of rat nNOS, bovine eNOS, and rat iNOS are 0.71, 0.78, and 5.8 µM, respectively.{1339}  

     

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    Cayman
    SKU:81340 - 250 mg

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  • 7-Nitroindazole is a non-selective inhibitor of NOS isoforms in vitro. However, it shows good anti-nociceptive effects in vivo without affecting blood pressure via inhibition of eNOS.{1220} The IC50 values for inhibition of rat nNOS, bovine eNOS, and rat iNOS are 0.71, 0.78, and 5.8 µM, respectively.{1339}  

     

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    Cayman
    SKU:81340 - 50 mg

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  • 7-Nitroindazole is a non-selective inhibitor of NOS isoforms in vitro. However, it shows good anti-nociceptive effects in vivo without affecting blood pressure via inhibition of eNOS.{1220} The IC50 values for inhibition of rat nNOS, bovine eNOS, and rat iNOS are 0.71, 0.78, and 5.8 µM, respectively.{1339}  

     

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    Cayman
    SKU:81340 - 500 mg

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  • 7-oxo Staurosporine is an antibiotic originally isolated from S. platensis with diverse biological activites.{41405,41406,41407,41409} It inhibits PKC, PKA, phosphorylase kinase, EGFR, and c-Src in vitro (IC50s = 9, 26, 5, 200, and 800 nM, respectively).{41406} 7-oxo Staurosporine induces cell cycle arrest in the G2/M phase in human leukemia K562 cells with a minimal effective dose (MED) of 30 ng/ml.{41405} It is cytotoxic to P388 mouse leukemia cells that are resistant and susceptible to doxorubicin (Item No. 15007; IC50s = 27 and 45 nM, respectively).{41407} 7-oxo Staurosporine inhibits growth of the mycelial, but not yeast form of C. albicans, C. krusei, C. tropicalis, and C. lusitaniae (MICs = 3.1-25 μg/ml).{41408} It increases sphingomyelin synthesis in CHO-K1 cells when used at a concentration of 50 nM.{41409}  

     

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    Cayman
    SKU:23346 - 1 mg

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  • 7-oxo Staurosporine is an antibiotic originally isolated from S. platensis with diverse biological activites.{41405,41406,41407,41409} It inhibits PKC, PKA, phosphorylase kinase, EGFR, and c-Src in vitro (IC50s = 9, 26, 5, 200, and 800 nM, respectively).{41406} 7-oxo Staurosporine induces cell cycle arrest in the G2/M phase in human leukemia K562 cells with a minimal effective dose (MED) of 30 ng/ml.{41405} It is cytotoxic to P388 mouse leukemia cells that are resistant and susceptible to doxorubicin (Item No. 15007; IC50s = 27 and 45 nM, respectively).{41407} 7-oxo Staurosporine inhibits growth of the mycelial, but not yeast form of C. albicans, C. krusei, C. tropicalis, and C. lusitaniae (MICs = 3.1-25 μg/ml).{41408} It increases sphingomyelin synthesis in CHO-K1 cells when used at a concentration of 50 nM.{41409}  

     

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    Cayman
    SKU:23346 - 5 mg

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  • tert-butyl p-Toluate is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    Cayman
    SKU:10007136 - 100 mg

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  • tert-butyl p-Toluate is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    Cayman
    SKU:10007136 - 250 mg

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  • tert-butyl p-Toluate is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    SKU:10007136 - 50 mg

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  • tert-butyl p-Toluate is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    Cayman
    SKU:10007136 - 500 mg

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  • 7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.{58173,58171} It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adducts in vivo, and it has been commonly used to induce tumor formation in various rodent models.{58171,58172,58173} DMBA increases proliferation and migration of, and induces epithelial-to-mesenchymal transition (EMT) in, MCF-10A breast cancer cells when used at a concentration of 5 µM.{58174} It also has immunosuppressant activity, inhibiting proliferation of isolated mouse splenic B- and T cells stimulated ex vivo with LPS or concanavalin A (Item No. 14951), respectively, when administered at doses of 50 and 100 mg/kg.{58175} Intragastric administration of DMBA (20 mg/animal) induces formation of mammary gland tumors in rats.{58176} DMBA (50 µg/animal), in combination with phorbol 12-myristate 13-acetate (TPA; Item No. 10008014), initiates papilloma formation in a rat two-stage model of skin carcinogenesis.{58177}  

     

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    Cayman
    SKU:30383 - 1 g

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  • 7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.{58173,58171} It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adducts in vivo, and it has been commonly used to induce tumor formation in various rodent models.{58171,58172,58173} DMBA increases proliferation and migration of, and induces epithelial-to-mesenchymal transition (EMT) in, MCF-10A breast cancer cells when used at a concentration of 5 µM.{58174} It also has immunosuppressant activity, inhibiting proliferation of isolated mouse splenic B- and T cells stimulated ex vivo with LPS or concanavalin A (Item No. 14951), respectively, when administered at doses of 50 and 100 mg/kg.{58175} Intragastric administration of DMBA (20 mg/animal) induces formation of mammary gland tumors in rats.{58176} DMBA (50 µg/animal), in combination with phorbol 12-myristate 13-acetate (TPA; Item No. 10008014), initiates papilloma formation in a rat two-stage model of skin carcinogenesis.{58177}  

     

    Brand:
    Cayman
    SKU:30383 - 100 mg

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  • 7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.{58173,58171} It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adducts in vivo, and it has been commonly used to induce tumor formation in various rodent models.{58171,58172,58173} DMBA increases proliferation and migration of, and induces epithelial-to-mesenchymal transition (EMT) in, MCF-10A breast cancer cells when used at a concentration of 5 µM.{58174} It also has immunosuppressant activity, inhibiting proliferation of isolated mouse splenic B- and T cells stimulated ex vivo with LPS or concanavalin A (Item No. 14951), respectively, when administered at doses of 50 and 100 mg/kg.{58175} Intragastric administration of DMBA (20 mg/animal) induces formation of mammary gland tumors in rats.{58176} DMBA (50 µg/animal), in combination with phorbol 12-myristate 13-acetate (TPA; Item No. 10008014), initiates papilloma formation in a rat two-stage model of skin carcinogenesis.{58177}  

     

    Brand:
    Cayman
    SKU:30383 - 250 mg

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  • 7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.{58173,58171} It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adducts in vivo, and it has been commonly used to induce tumor formation in various rodent models.{58171,58172,58173} DMBA increases proliferation and migration of, and induces epithelial-to-mesenchymal transition (EMT) in, MCF-10A breast cancer cells when used at a concentration of 5 µM.{58174} It also has immunosuppressant activity, inhibiting proliferation of isolated mouse splenic B- and T cells stimulated ex vivo with LPS or concanavalin A (Item No. 14951), respectively, when administered at doses of 50 and 100 mg/kg.{58175} Intragastric administration of DMBA (20 mg/animal) induces formation of mammary gland tumors in rats.{58176} DMBA (50 µg/animal), in combination with phorbol 12-myristate 13-acetate (TPA; Item No. 10008014), initiates papilloma formation in a rat two-stage model of skin carcinogenesis.{58177}  

     

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    SKU:30383 - 500 mg

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  • 7,3’,4’-Trihydroxyflavone is a flavonoid that has been found in A. julibrissin bark and has diverse biological activities.{52324,52325,52326,52327} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) and peroxynitrite radicals in cell-free assays (IC50s = 2.2 and 5.78 µM, respectively), as well as reduces total reactive oxygen species in rat kidney homogenates (IC50 = 3.9 µM).{52324} 7,3’,4’-Trihydroxyflavone inhibits COX-1 (IC50 = 36.7 µM).{52325} It is active against M. tuberculosis (MIC = 50 µg/ml).{52326} It decreases mRNA expression of the osteoclastic marker genes encoding the calcitonin receptor, cathepsin K1 V-ATPase V0 subunit d2 (Atp6v0d2), and dendritic cell specific transmembrane protein (Dcstamp) in and inhibits RANKL-induced osteoclastic differentiation of mouse bone marrow-derived macrophages (BMDMs).{52327}  

     

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    SKU:29880 - 100 mg

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  • 7,3’,4’-Trihydroxyflavone is a flavonoid that has been found in A. julibrissin bark and has diverse biological activities.{52324,52325,52326,52327} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) and peroxynitrite radicals in cell-free assays (IC50s = 2.2 and 5.78 µM, respectively), as well as reduces total reactive oxygen species in rat kidney homogenates (IC50 = 3.9 µM).{52324} 7,3’,4’-Trihydroxyflavone inhibits COX-1 (IC50 = 36.7 µM).{52325} It is active against M. tuberculosis (MIC = 50 µg/ml).{52326} It decreases mRNA expression of the osteoclastic marker genes encoding the calcitonin receptor, cathepsin K1 V-ATPase V0 subunit d2 (Atp6v0d2), and dendritic cell specific transmembrane protein (Dcstamp) in and inhibits RANKL-induced osteoclastic differentiation of mouse bone marrow-derived macrophages (BMDMs).{52327}  

     

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    SKU:29880 - 25 mg

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  • 7,3’,4’-Trihydroxyflavone is a flavonoid that has been found in A. julibrissin bark and has diverse biological activities.{52324,52325,52326,52327} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) and peroxynitrite radicals in cell-free assays (IC50s = 2.2 and 5.78 µM, respectively), as well as reduces total reactive oxygen species in rat kidney homogenates (IC50 = 3.9 µM).{52324} 7,3’,4’-Trihydroxyflavone inhibits COX-1 (IC50 = 36.7 µM).{52325} It is active against M. tuberculosis (MIC = 50 µg/ml).{52326} It decreases mRNA expression of the osteoclastic marker genes encoding the calcitonin receptor, cathepsin K1 V-ATPase V0 subunit d2 (Atp6v0d2), and dendritic cell specific transmembrane protein (Dcstamp) in and inhibits RANKL-induced osteoclastic differentiation of mouse bone marrow-derived macrophages (BMDMs).{52327}  

     

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    SKU:29880 - 50 mg

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  • BH2 is a precursor of BH4 synthesis. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 µM.{1268}  

     

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    SKU:81882 - 10 mg

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  • BH2 is a precursor of BH4 synthesis. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 µM.{1268}  

     

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    SKU:81882 - 100 mg

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  • BH2 is a precursor of BH4 synthesis. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 µM.{1268}  

     

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    SKU:81882 - 5 mg

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  • BH2 is a precursor of BH4 synthesis. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 µM.{1268}  

     

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    SKU:81882 - 50 mg

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  • 7,8-Dihydroneopterin is a pteridine with antioxidant activities.{47629} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in a cell-free assay when used at concentrations ranging from 20 to 100 µM. 7,8-Dihydroneopterin (2-10 µM) inhibits copper ion-induced oxidation of LDL in a cell-free assay and decreases thiobarbituric acid reactive substances (TBARS) produced by THP-1 cells cultured with LDL.{47630,47631} It inhibits necrosis induced by oxidized LDL (oxLDL) in U937, but not THP-1, cells when used at a concentration of 200 µM.{47632}  

     

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    Cayman
    SKU:27606 - 10 mg

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  • 7,8-Dihydroneopterin is a pteridine with antioxidant activities.{47629} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in a cell-free assay when used at concentrations ranging from 20 to 100 µM. 7,8-Dihydroneopterin (2-10 µM) inhibits copper ion-induced oxidation of LDL in a cell-free assay and decreases thiobarbituric acid reactive substances (TBARS) produced by THP-1 cells cultured with LDL.{47630,47631} It inhibits necrosis induced by oxidized LDL (oxLDL) in U937, but not THP-1, cells when used at a concentration of 200 µM.{47632}  

     

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    Cayman
    SKU:27606 - 25 mg

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  • 7,8-Dihydroneopterin is a pteridine with antioxidant activities.{47629} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in a cell-free assay when used at concentrations ranging from 20 to 100 µM. 7,8-Dihydroneopterin (2-10 µM) inhibits copper ion-induced oxidation of LDL in a cell-free assay and decreases thiobarbituric acid reactive substances (TBARS) produced by THP-1 cells cultured with LDL.{47630,47631} It inhibits necrosis induced by oxidized LDL (oxLDL) in U937, but not THP-1, cells when used at a concentration of 200 µM.{47632}  

     

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    Cayman
    SKU:27606 - 5 mg

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  • 7,8-Dihydroxyflavone (7,8-DHF) is a monophenolic flavone with diverse effects. It acts as an agonist of the neurotrophic tyrosine kinase receptor TrkB (Kd = 320 nM), protecting neurons that express TrkB from apoptosis.{27651} 7,8-DHF is neuroprotective in an animal model of Parkinson’s disease.{27651} It supports emotional learning in mice and reverses memory deficits in a mouse model of Alzheimer’s disease.{27655,27653} It also improves motor function and extends survival in an animal model of Huntington’s disease.{27650} 7,8-DHF inhibits the cytochrome P450 aromatase (IC50 = 10 µM) and, in this way, alters estrogen metabolism.{27652} It also has antioxidant action that increases intracellular glutathione synthesis and scavenges reactive oxygen species.{27654}  

     

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    Cayman
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  • 7,8-Dihydroxyflavone (7,8-DHF) is a monophenolic flavone with diverse effects. It acts as an agonist of the neurotrophic tyrosine kinase receptor TrkB (Kd = 320 nM), protecting neurons that express TrkB from apoptosis.{27651} 7,8-DHF is neuroprotective in an animal model of Parkinson’s disease.{27651} It supports emotional learning in mice and reverses memory deficits in a mouse model of Alzheimer’s disease.{27655,27653} It also improves motor function and extends survival in an animal model of Huntington’s disease.{27650} 7,8-DHF inhibits the cytochrome P450 aromatase (IC50 = 10 µM) and, in this way, alters estrogen metabolism.{27652} It also has antioxidant action that increases intracellular glutathione synthesis and scavenges reactive oxygen species.{27654}  

     

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    Cayman
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  • 7,8-Dihydroxyflavone (7,8-DHF) is a monophenolic flavone with diverse effects. It acts as an agonist of the neurotrophic tyrosine kinase receptor TrkB (Kd = 320 nM), protecting neurons that express TrkB from apoptosis.{27651} 7,8-DHF is neuroprotective in an animal model of Parkinson’s disease.{27651} It supports emotional learning in mice and reverses memory deficits in a mouse model of Alzheimer’s disease.{27655,27653} It also improves motor function and extends survival in an animal model of Huntington’s disease.{27650} 7,8-DHF inhibits the cytochrome P450 aromatase (IC50 = 10 µM) and, in this way, alters estrogen metabolism.{27652} It also has antioxidant action that increases intracellular glutathione synthesis and scavenges reactive oxygen species.{27654}  

     

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    Cayman
    SKU:-

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  • 7,8-Dihydroxyflavone (7,8-DHF) is a monophenolic flavone with diverse effects. It acts as an agonist of the neurotrophic tyrosine kinase receptor TrkB (Kd = 320 nM), protecting neurons that express TrkB from apoptosis.{27651} 7,8-DHF is neuroprotective in an animal model of Parkinson’s disease.{27651} It supports emotional learning in mice and reverses memory deficits in a mouse model of Alzheimer’s disease.{27655,27653} It also improves motor function and extends survival in an animal model of Huntington’s disease.{27650} 7,8-DHF inhibits the cytochrome P450 aromatase (IC50 = 10 µM) and, in this way, alters estrogen metabolism.{27652} It also has antioxidant action that increases intracellular glutathione synthesis and scavenges reactive oxygen species.{27654}  

     

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    Cayman
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  • 7,8,9,10-Tetrahydrobenzo[a]pyren-7-ol is a benzopyrene derivative that is activated by hepatic cytosol into electrophilic sulfuric acid esters, which are capable of forming covalent DNA adducts and inducing mutations.{26509,26510}  

     

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    Cayman
    SKU:-
  • 7,8,9,10-Tetrahydrobenzo[a]pyren-7-ol is a benzopyrene derivative that is activated by hepatic cytosol into electrophilic sulfuric acid esters, which are capable of forming covalent DNA adducts and inducing mutations.{26509,26510}  

     

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    Cayman
    SKU:-
  • 7,8,9,10-Tetrahydrobenzo[a]pyren-7-ol is a benzopyrene derivative that is activated by hepatic cytosol into electrophilic sulfuric acid esters, which are capable of forming covalent DNA adducts and inducing mutations.{26509,26510}  

     

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    SKU:-
  • 7′-methoxy NABUTIE (Item No. 22630) is an analytical reference standard categorized as a synthetic cannabinoid.{23277} This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:22630 -

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  • 7′-methoxy NABUTIE (Item No. 22630) is an analytical reference standard categorized as a synthetic cannabinoid.{23277} This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:22630 -

    Out of stock

  • Novel oxylipins, referred to as docosanoids, have been derived from C22 polyunsaturated fatty acids 7(S),17(S)-dihydroxy-8(E),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic acid (7(S),17(S)-hydroxy DPA) is a DPA-derived analog of the 17(S)-dihydroxy series of docosanoids known as protectins. Protectin D1, a DHA-derived dihydroxy fatty acid, exhibits potent anti-inflammatory activities.{14974,14973,14972} Potentially, 7(S),17(S)-hydroxy DPA demonstrates similar properties; however, its biological activity has yet to be determined.  

     

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    Cayman
    SKU:10546 - 100 µg

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  • Novel oxylipins, referred to as docosanoids, have been derived from C22 polyunsaturated fatty acids 7(S),17(S)-dihydroxy-8(E),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic acid (7(S),17(S)-hydroxy DPA) is a DPA-derived analog of the 17(S)-dihydroxy series of docosanoids known as protectins. Protectin D1, a DHA-derived dihydroxy fatty acid, exhibits potent anti-inflammatory activities.{14974,14973,14972} Potentially, 7(S),17(S)-hydroxy DPA demonstrates similar properties; however, its biological activity has yet to be determined.  

     

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    Cayman
    SKU:10546 - 25 µg

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  • Novel oxylipins, referred to as docosanoids, have been derived from C22 polyunsaturated fatty acids 7(S),17(S)-dihydroxy-8(E),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic acid (7(S),17(S)-hydroxy DPA) is a DPA-derived analog of the 17(S)-dihydroxy series of docosanoids known as protectins. Protectin D1, a DHA-derived dihydroxy fatty acid, exhibits potent anti-inflammatory activities.{14974,14973,14972} Potentially, 7(S),17(S)-hydroxy DPA demonstrates similar properties; however, its biological activity has yet to be determined.  

     

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    Cayman
    SKU:10546 - 50 µg

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  • 7(Z)-Pentacosene is an unsaturated cuticular hydrocarbon that acts as a contact sex pheromone in fruit flies. In different species and genotypes of Drosophila, it can be found on both males and females.{16828,17569,17568} Pentacosene may stimulate copulation either by itself at high concentrations{16279} or when combined with other alkenes. Interestingly, the absolute level of pentacosene increases in Drosophila females immediately after copulation.{17568,16828}  

     

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    Cayman
    SKU:9000530 - 1 mg

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  • 7(Z)-Pentacosene is an unsaturated cuticular hydrocarbon that acts as a contact sex pheromone in fruit flies. In different species and genotypes of Drosophila, it can be found on both males and females.{16828,17569,17568} Pentacosene may stimulate copulation either by itself at high concentrations{16279} or when combined with other alkenes. Interestingly, the absolute level of pentacosene increases in Drosophila females immediately after copulation.{17568,16828}  

     

    Brand:
    Cayman
    SKU:9000530 - 10 mg

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  • 7(Z)-Pentacosene is an unsaturated cuticular hydrocarbon that acts as a contact sex pheromone in fruit flies. In different species and genotypes of Drosophila, it can be found on both males and females.{16828,17569,17568} Pentacosene may stimulate copulation either by itself at high concentrations{16279} or when combined with other alkenes. Interestingly, the absolute level of pentacosene increases in Drosophila females immediately after copulation.{17568,16828}  

     

    Brand:
    Cayman
    SKU:9000530 - 5 mg

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  • 7(Z)-Pentacosene is an unsaturated cuticular hydrocarbon that acts as a contact sex pheromone in fruit flies. In different species and genotypes of Drosophila, it can be found on both males and females.{16828,17569,17568} Pentacosene may stimulate copulation either by itself at high concentrations{16279} or when combined with other alkenes. Interestingly, the absolute level of pentacosene increases in Drosophila females immediately after copulation.{17568,16828}  

     

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    Cayman
    SKU:9000530 - 50 mg

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  • 7(Z)-Tricosene is an unsaturated cuticular hydrocarbon that acts as a pheromone in some insects, including Drosophila. While it is present in both sexes of some Drosophila species, it is abundant in males, but not females, of D. melanogaster and D. sechellia.{16894} In these species, 7(Z)-tricosene prevents or reduces male courtship behavior{16914} and increases female sexual receptivity.{16915} It is absent from virgin D. melanogaster females, but is transferred from males to females during mating.{16916} In addition, mating induces the synthesis of 7(Z)-tricosene by D. melanogaster females, so that it acts as an anti-aphrodisiac in mated females.{16916} 7(Z)-Tricosene is also a minor component of labial gland secretion and cuticle of Bombus spp.{16895,16896}  

     

    Brand:
    Cayman
    SKU:9000313 - 1 mg

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  • 7(Z)-Tricosene is an unsaturated cuticular hydrocarbon that acts as a pheromone in some insects, including Drosophila. While it is present in both sexes of some Drosophila species, it is abundant in males, but not females, of D. melanogaster and D. sechellia.{16894} In these species, 7(Z)-tricosene prevents or reduces male courtship behavior{16914} and increases female sexual receptivity.{16915} It is absent from virgin D. melanogaster females, but is transferred from males to females during mating.{16916} In addition, mating induces the synthesis of 7(Z)-tricosene by D. melanogaster females, so that it acts as an anti-aphrodisiac in mated females.{16916} 7(Z)-Tricosene is also a minor component of labial gland secretion and cuticle of Bombus spp.{16895,16896}  

     

    Brand:
    Cayman
    SKU:9000313 - 10 mg

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  • 7(Z)-Tricosene is an unsaturated cuticular hydrocarbon that acts as a pheromone in some insects, including Drosophila. While it is present in both sexes of some Drosophila species, it is abundant in males, but not females, of D. melanogaster and D. sechellia.{16894} In these species, 7(Z)-tricosene prevents or reduces male courtship behavior{16914} and increases female sexual receptivity.{16915} It is absent from virgin D. melanogaster females, but is transferred from males to females during mating.{16916} In addition, mating induces the synthesis of 7(Z)-tricosene by D. melanogaster females, so that it acts as an anti-aphrodisiac in mated females.{16916} 7(Z)-Tricosene is also a minor component of labial gland secretion and cuticle of Bombus spp.{16895,16896}  

     

    Brand:
    Cayman
    SKU:9000313 - 5 mg

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  • 7(Z)-Tricosene is an unsaturated cuticular hydrocarbon that acts as a pheromone in some insects, including Drosophila. While it is present in both sexes of some Drosophila species, it is abundant in males, but not females, of D. melanogaster and D. sechellia.{16894} In these species, 7(Z)-tricosene prevents or reduces male courtship behavior{16914} and increases female sexual receptivity.{16915} It is absent from virgin D. melanogaster females, but is transferred from males to females during mating.{16916} In addition, mating induces the synthesis of 7(Z)-tricosene by D. melanogaster females, so that it acts as an anti-aphrodisiac in mated females.{16916} 7(Z)-Tricosene is also a minor component of labial gland secretion and cuticle of Bombus spp.{16895,16896}  

     

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    Cayman
    SKU:9000313 - 50 mg

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  • 4(Z),7(Z),10(Z),13(Z),16(Z)-N-(2-hydroxyethyl)-Docosapentaenamide is a long-chain ω-3 fatty acid with a hydroxyethylamide group attached at the alpha chain.  

     

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    Cayman
    SKU:-
  • 4(Z),7(Z),10(Z),13(Z),16(Z)-N-(2-hydroxyethyl)-Docosapentaenamide is a long-chain ω-3 fatty acid with a hydroxyethylamide group attached at the alpha chain.  

     

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    Cayman
    SKU:-
  • 4(Z),7(Z),10(Z),13(Z),16(Z)-N-(2-hydroxyethyl)-Docosapentaenamide is a long-chain ω-3 fatty acid with a hydroxyethylamide group attached at the alpha chain.  

     

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    Cayman
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  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile cuticular hydrocarbon pheromones. 7(Z),11(Z)-Heptacosadiene is the predominant female-specific courtship pheromone of the fruit fly D. melanogaster. At amounts above 100 ng, 7(Z),11(Z)-heptacosadiene elicits wing vibrations in male D. melanogaster flies in a dose-dependent manner.{16279}  

     

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    Cayman
    SKU:10012567 - 1 mg

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  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile cuticular hydrocarbon pheromones. 7(Z),11(Z)-Heptacosadiene is the predominant female-specific courtship pheromone of the fruit fly D. melanogaster. At amounts above 100 ng, 7(Z),11(Z)-heptacosadiene elicits wing vibrations in male D. melanogaster flies in a dose-dependent manner.{16279}  

     

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    Cayman
    SKU:10012567 - 10 mg

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  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile cuticular hydrocarbon pheromones. 7(Z),11(Z)-Heptacosadiene is the predominant female-specific courtship pheromone of the fruit fly D. melanogaster. At amounts above 100 ng, 7(Z),11(Z)-heptacosadiene elicits wing vibrations in male D. melanogaster flies in a dose-dependent manner.{16279}  

     

    Brand:
    Cayman
    SKU:10012567 - 5 mg

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  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile cuticular hydrocarbon pheromones. 7(Z),11(Z)-Heptacosadiene is the predominant female-specific courtship pheromone of the fruit fly D. melanogaster. At amounts above 100 ng, 7(Z),11(Z)-heptacosadiene elicits wing vibrations in male D. melanogaster flies in a dose-dependent manner.{16279}  

     

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    Cayman
    SKU:10012567 - 50 mg

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  • Unsaturated cuticular hydrocarbons serve as pheromones in insects. In D. melanogaster, these hydrocarbons are sexually dimorphic in both their occurrence and their effects. 7(Z),11(Z)-Nonacosadiene is a cuticular pheromone in female fruit flies that stimulates male courtship behavior.{16828} The biosynthesis of this C29 diene appears to be mediated by an elongase with female-based expression.{16827}  

     

    Brand:
    Cayman
    SKU:9000314 - 1 mg

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  • Unsaturated cuticular hydrocarbons serve as pheromones in insects. In D. melanogaster, these hydrocarbons are sexually dimorphic in both their occurrence and their effects. 7(Z),11(Z)-Nonacosadiene is a cuticular pheromone in female fruit flies that stimulates male courtship behavior.{16828} The biosynthesis of this C29 diene appears to be mediated by an elongase with female-based expression.{16827}  

     

    Brand:
    Cayman
    SKU:9000314 - 10 mg

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  • Unsaturated cuticular hydrocarbons serve as pheromones in insects. In D. melanogaster, these hydrocarbons are sexually dimorphic in both their occurrence and their effects. 7(Z),11(Z)-Nonacosadiene is a cuticular pheromone in female fruit flies that stimulates male courtship behavior.{16828} The biosynthesis of this C29 diene appears to be mediated by an elongase with female-based expression.{16827}  

     

    Brand:
    Cayman
    SKU:9000314 - 5 mg

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  • Unsaturated cuticular hydrocarbons serve as pheromones in insects. In D. melanogaster, these hydrocarbons are sexually dimorphic in both their occurrence and their effects. 7(Z),11(Z)-Nonacosadiene is a cuticular pheromone in female fruit flies that stimulates male courtship behavior.{16828} The biosynthesis of this C29 diene appears to be mediated by an elongase with female-based expression.{16827}  

     

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    Cayman
    SKU:9000314 - 50 mg

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  • Unsaturated, long-chain hydrocarbons are found on the cuticles of insects and can act as pheromones. In mature Drosophila melanogaster, certain cuticular hydrocarbons are sexually dimorphic: males synthesize 23- and 25-C monoenes and females produce 27- and 29-C dienes. Each of these lipids plays specific roles in regulating male sexual behavior, with dienes stimulating courtship.{16828} 7(Z),11(Z)-Pentacosadiene is a 25-C hydrocarbon that is found in low abundance on cuticles of mature Drosophila females.{17569} Depletion of a female-specific elongase (eloF), which leads to an increase in 7(Z),11(Z)-pentacosadiene along with a parallel decrease in 7,11-nonacosadiene, significantly reduces copulation in Drosophila.{16827} This raises the possibility that 7(Z),11(Z)-pentacosadiene may act as an anti-aphrodisiac.  

     

    Brand:
    Cayman
    SKU:9000531 - 1 mg

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  • Unsaturated, long-chain hydrocarbons are found on the cuticles of insects and can act as pheromones. In mature Drosophila melanogaster, certain cuticular hydrocarbons are sexually dimorphic: males synthesize 23- and 25-C monoenes and females produce 27- and 29-C dienes. Each of these lipids plays specific roles in regulating male sexual behavior, with dienes stimulating courtship.{16828} 7(Z),11(Z)-Pentacosadiene is a 25-C hydrocarbon that is found in low abundance on cuticles of mature Drosophila females.{17569} Depletion of a female-specific elongase (eloF), which leads to an increase in 7(Z),11(Z)-pentacosadiene along with a parallel decrease in 7,11-nonacosadiene, significantly reduces copulation in Drosophila.{16827} This raises the possibility that 7(Z),11(Z)-pentacosadiene may act as an anti-aphrodisiac.  

     

    Brand:
    Cayman
    SKU:9000531 - 10 mg

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  • Unsaturated, long-chain hydrocarbons are found on the cuticles of insects and can act as pheromones. In mature Drosophila melanogaster, certain cuticular hydrocarbons are sexually dimorphic: males synthesize 23- and 25-C monoenes and females produce 27- and 29-C dienes. Each of these lipids plays specific roles in regulating male sexual behavior, with dienes stimulating courtship.{16828} 7(Z),11(Z)-Pentacosadiene is a 25-C hydrocarbon that is found in low abundance on cuticles of mature Drosophila females.{17569} Depletion of a female-specific elongase (eloF), which leads to an increase in 7(Z),11(Z)-pentacosadiene along with a parallel decrease in 7,11-nonacosadiene, significantly reduces copulation in Drosophila.{16827} This raises the possibility that 7(Z),11(Z)-pentacosadiene may act as an anti-aphrodisiac.  

     

    Brand:
    Cayman
    SKU:9000531 - 5 mg

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  • Unsaturated, long-chain hydrocarbons are found on the cuticles of insects and can act as pheromones. In mature Drosophila melanogaster, certain cuticular hydrocarbons are sexually dimorphic: males synthesize 23- and 25-C monoenes and females produce 27- and 29-C dienes. Each of these lipids plays specific roles in regulating male sexual behavior, with dienes stimulating courtship.{16828} 7(Z),11(Z)-Pentacosadiene is a 25-C hydrocarbon that is found in low abundance on cuticles of mature Drosophila females.{17569} Depletion of a female-specific elongase (eloF), which leads to an increase in 7(Z),11(Z)-pentacosadiene along with a parallel decrease in 7,11-nonacosadiene, significantly reduces copulation in Drosophila.{16827} This raises the possibility that 7(Z),11(Z)-pentacosadiene may act as an anti-aphrodisiac.  

     

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    Cayman
    SKU:9000531 - 50 mg

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  • 740 Y-P is a peptide activator of phosphatidylinositol 3-kinase (PI3K).{37145} It binds to the p85 N- and C-terminal SH2 domains of PI3K but not to GST or the N-terminal domain of phospholipase C (PLC) in an affinity purification assay. 740 Y-P is cell-permeable and stimulates mitogenesis in serum-starved C2 cells at a concentration of 50 μg/ml. This effect is abolished by treatment with 10 μM wortmannin (Item No. 10010591), a PI3K inhibitor, indicating 740 Y-P is interacting specifically with PI3K in cells. 740 Y-P also reverses inhibition of PI3K by schisandrin B in U251 and U87 melanoma cells, inducing expression of phosphorylated mammalian target of rapamycin (p-mTOR) and matrix metalloproteinase-9 (MMP-9).{37146}  

     

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    Cayman
    SKU:22598 -

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  • 740 Y-P is a peptide activator of phosphatidylinositol 3-kinase (PI3K).{37145} It binds to the p85 N- and C-terminal SH2 domains of PI3K but not to GST or the N-terminal domain of phospholipase C (PLC) in an affinity purification assay. 740 Y-P is cell-permeable and stimulates mitogenesis in serum-starved C2 cells at a concentration of 50 μg/ml. This effect is abolished by treatment with 10 μM wortmannin (Item No. 10010591), a PI3K inhibitor, indicating 740 Y-P is interacting specifically with PI3K in cells. 740 Y-P also reverses inhibition of PI3K by schisandrin B in U251 and U87 melanoma cells, inducing expression of phosphorylated mammalian target of rapamycin (p-mTOR) and matrix metalloproteinase-9 (MMP-9).{37146}  

     

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    Cayman
    SKU:22598 -

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  • 7ACC2 is a carboxycoumarin inhibitor of monocarboxylate transporter 1 (MCT1) with an IC50 value of 10 nM for lactate uptake, an MCT1-dependent process, in SiHa human cervix carcinoma cells.{36195} It inhibits proliferation of SiHa cells in the presence of lactate in a dose-dependent manner but lacks cytotoxicity in the presence of glucose. 7ACC2 also inhibits the mitochondrial pyruvate carrier (MPC) in a concentration- and time-dependent manner in isolated tumor cell mitochondria.{46097} In vivo, 7ACC2 (3 mg/kg) increases intratumor lactate accumulation and decreases tumor size in an SiHa mouse xenograft model.  

     

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    Cayman
    SKU:23445 - 1 mg

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  • 7ACC2 is a carboxycoumarin inhibitor of monocarboxylate transporter 1 (MCT1) with an IC50 value of 10 nM for lactate uptake, an MCT1-dependent process, in SiHa human cervix carcinoma cells.{36195} It inhibits proliferation of SiHa cells in the presence of lactate in a dose-dependent manner but lacks cytotoxicity in the presence of glucose. 7ACC2 also inhibits the mitochondrial pyruvate carrier (MPC) in a concentration- and time-dependent manner in isolated tumor cell mitochondria.{46097} In vivo, 7ACC2 (3 mg/kg) increases intratumor lactate accumulation and decreases tumor size in an SiHa mouse xenograft model.  

     

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    Cayman
    SKU:23445 - 10 mg

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  • 7ACC2 is a carboxycoumarin inhibitor of monocarboxylate transporter 1 (MCT1) with an IC50 value of 10 nM for lactate uptake, an MCT1-dependent process, in SiHa human cervix carcinoma cells.{36195} It inhibits proliferation of SiHa cells in the presence of lactate in a dose-dependent manner but lacks cytotoxicity in the presence of glucose. 7ACC2 also inhibits the mitochondrial pyruvate carrier (MPC) in a concentration- and time-dependent manner in isolated tumor cell mitochondria.{46097} In vivo, 7ACC2 (3 mg/kg) increases intratumor lactate accumulation and decreases tumor size in an SiHa mouse xenograft model.  

     

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    Cayman
    SKU:23445 - 25 mg

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  • 7ACC2 is a carboxycoumarin inhibitor of monocarboxylate transporter 1 (MCT1) with an IC50 value of 10 nM for lactate uptake, an MCT1-dependent process, in SiHa human cervix carcinoma cells.{36195} It inhibits proliferation of SiHa cells in the presence of lactate in a dose-dependent manner but lacks cytotoxicity in the presence of glucose. 7ACC2 also inhibits the mitochondrial pyruvate carrier (MPC) in a concentration- and time-dependent manner in isolated tumor cell mitochondria.{46097} In vivo, 7ACC2 (3 mg/kg) increases intratumor lactate accumulation and decreases tumor size in an SiHa mouse xenograft model.  

     

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    Cayman
    SKU:23445 - 5 mg

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  • 7BIO is a derivative of indirubin (Item No. 14155) that triggers a rapid cell death process that is distinct from apoptosis and devoid of cytochrome c release or caspase activation.{31285} Furthermore, in contrast to other indirubin derivatives, 7BIO has only marginal activity against the classic indirubin targets, cyclin-dependent kinases and GSK3.{31285,22470} Instead, 7BIO inhibits FLT3 (IC50 = 0.34 µM) and the dual-specificity tyrosine phosphorylation-regulated kinases, DYRK1A and DYRK2 (IC50s = 1.9 and 1.3 µM, respectively).{31285,31284} It also inhibits Aurora B and C kinases with IC50 values of 4.6 and 0.7 µM, respectively.{31285,31283}  

     

    Brand:
    Cayman
    SKU:19619 -

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  • 7BIO is a derivative of indirubin (Item No. 14155) that triggers a rapid cell death process that is distinct from apoptosis and devoid of cytochrome c release or caspase activation.{31285} Furthermore, in contrast to other indirubin derivatives, 7BIO has only marginal activity against the classic indirubin targets, cyclin-dependent kinases and GSK3.{31285,22470} Instead, 7BIO inhibits FLT3 (IC50 = 0.34 µM) and the dual-specificity tyrosine phosphorylation-regulated kinases, DYRK1A and DYRK2 (IC50s = 1.9 and 1.3 µM, respectively).{31285,31284} It also inhibits Aurora B and C kinases with IC50 values of 4.6 and 0.7 µM, respectively.{31285,31283}  

     

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    Cayman
    SKU:19619 -

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  • 7Z,10Z,13Z,16Z-Docosatetraenoic acid is a naturally occurring polyunsaturated fatty acid (PUFA) formed through a 2-carbon chain elongation of arachidonic acid. It is present in the adrenal glands, brain, testis, and kidney.{1288} Although there is trace metabolism of adrenic acid in the forebrain, the renal medulla is the only tissue which readily metabolizes the acid through cyclooxygenase activity.{1288,2047} The primary metabolite of 7Z,10Z,13Z,16Z-docosatetraenoic acid in the rabbit kidney is 1a,1b-dihomo prostaglandin E2.{1288}  

     

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    Cayman
    SKU:90300 - 10 mg

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  • 7Z,10Z,13Z,16Z-Docosatetraenoic acid is a naturally occurring polyunsaturated fatty acid (PUFA) formed through a 2-carbon chain elongation of arachidonic acid. It is present in the adrenal glands, brain, testis, and kidney.{1288} Although there is trace metabolism of adrenic acid in the forebrain, the renal medulla is the only tissue which readily metabolizes the acid through cyclooxygenase activity.{1288,2047} The primary metabolite of 7Z,10Z,13Z,16Z-docosatetraenoic acid in the rabbit kidney is 1a,1b-dihomo prostaglandin E2.{1288}  

     

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    Cayman
    SKU:90300 - 100 mg

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  • 7Z,10Z,13Z,16Z-Docosatetraenoic acid is a naturally occurring polyunsaturated fatty acid (PUFA) formed through a 2-carbon chain elongation of arachidonic acid. It is present in the adrenal glands, brain, testis, and kidney.{1288} Although there is trace metabolism of adrenic acid in the forebrain, the renal medulla is the only tissue which readily metabolizes the acid through cyclooxygenase activity.{1288,2047} The primary metabolite of 7Z,10Z,13Z,16Z-docosatetraenoic acid in the rabbit kidney is 1a,1b-dihomo prostaglandin E2.{1288}  

     

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    Cayman
    SKU:90300 - 25 mg

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  • 7Z,10Z,13Z,16Z-Docosatetraenoic acid is a naturally occurring polyunsaturated fatty acid (PUFA) formed through a 2-carbon chain elongation of arachidonic acid. It is present in the adrenal glands, brain, testis, and kidney.{1288} Although there is trace metabolism of adrenic acid in the forebrain, the renal medulla is the only tissue which readily metabolizes the acid through cyclooxygenase activity.{1288,2047} The primary metabolite of 7Z,10Z,13Z,16Z-docosatetraenoic acid in the rabbit kidney is 1a,1b-dihomo prostaglandin E2.{1288}  

     

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    Cayman
    SKU:90300 - 50 mg

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  • 7α-hydroxy Cholesterol is an oxysterol and a precursor in the biosynthesis of the bile acids cholic acid (CA; Item No. 20250) and chenodeoxycholic acid (CDCA; Item No. 10011286).{42274,48225} It is formed via the oxidation of cholesterol (Item No. 9003100) by cholesterol 7α-hydroxylase/CYP7A1 in rat liver microsomes.{42274} 7α-hydroxy Cholesterol (40 µM) increases levels of the adhesion molecules ICAM-1, VCAM-1, and E-selectin in human umbilical vein endothelial cells (HUVECs).{60007} It increases secretion of chemokine (C-C motif) ligand 2 (CCL2) and matrix metalloproteinase-9 (MMP-9) in serum-deprived THP-1 cells when used at a concentration of 5 µg/ml.{42273} 7α-hydroxy Cholesterol has been found in macrophages isolated from atherosclerotic lesions in rabbits fed a high-cholesterol diet.{60008}  

     

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    SKU:20098 -

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  • 7α-hydroxy Cholesterol is an oxysterol and a precursor in the biosynthesis of the bile acids cholic acid (CA; Item No. 20250) and chenodeoxycholic acid (CDCA; Item No. 10011286).{42274,48225} It is formed via the oxidation of cholesterol (Item No. 9003100) by cholesterol 7α-hydroxylase/CYP7A1 in rat liver microsomes.{42274} 7α-hydroxy Cholesterol (40 µM) increases levels of the adhesion molecules ICAM-1, VCAM-1, and E-selectin in human umbilical vein endothelial cells (HUVECs).{60007} It increases secretion of chemokine (C-C motif) ligand 2 (CCL2) and matrix metalloproteinase-9 (MMP-9) in serum-deprived THP-1 cells when used at a concentration of 5 µg/ml.{42273} 7α-hydroxy Cholesterol has been found in macrophages isolated from atherosclerotic lesions in rabbits fed a high-cholesterol diet.{60008}  

     

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    SKU:20098 -

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  • 7α-hydroxy Cholesterol is an oxysterol and a precursor in the biosynthesis of the bile acids cholic acid (CA; Item No. 20250) and chenodeoxycholic acid (CDCA; Item No. 10011286).{42274,48225} It is formed via the oxidation of cholesterol (Item No. 9003100) by cholesterol 7α-hydroxylase/CYP7A1 in rat liver microsomes.{42274} 7α-hydroxy Cholesterol (40 µM) increases levels of the adhesion molecules ICAM-1, VCAM-1, and E-selectin in human umbilical vein endothelial cells (HUVECs).{60007} It increases secretion of chemokine (C-C motif) ligand 2 (CCL2) and matrix metalloproteinase-9 (MMP-9) in serum-deprived THP-1 cells when used at a concentration of 5 µg/ml.{42273} 7α-hydroxy Cholesterol has been found in macrophages isolated from atherosclerotic lesions in rabbits fed a high-cholesterol diet.{60008}  

     

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    Cayman
    SKU:20098 -

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  • 7α-hydroxy Cholesterol is an oxysterol and a precursor in the biosynthesis of the bile acids cholic acid (CA; Item No. 20250) and chenodeoxycholic acid (CDCA; Item No. 10011286).{42274,48225} It is formed via the oxidation of cholesterol (Item No. 9003100) by cholesterol 7α-hydroxylase/CYP7A1 in rat liver microsomes.{42274} 7α-hydroxy Cholesterol (40 µM) increases levels of the adhesion molecules ICAM-1, VCAM-1, and E-selectin in human umbilical vein endothelial cells (HUVECs).{60007} It increases secretion of chemokine (C-C motif) ligand 2 (CCL2) and matrix metalloproteinase-9 (MMP-9) in serum-deprived THP-1 cells when used at a concentration of 5 µg/ml.{42273} 7α-hydroxy Cholesterol has been found in macrophages isolated from atherosclerotic lesions in rabbits fed a high-cholesterol diet.{60008}  

     

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    Cayman
    SKU:20098 -

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  • 7α-hydroxy Cholesterol-d7 is intended for use as an internal standard for the quantification of 7α-hydroxy cholesterol (Item No. 20098) by GC- or LC-MS. 7α-hydroxy Cholesterol is an oxysterol and a precursor in the biosynthesis of the bile acids cholic acid (CA; Item No. 20250) and chenodeoxycholic acid (CDCA; Item No. 10011286).{42274,48225} It is formed via the oxidation of cholesterol (Item No. 9003100) by cholesterol 7α-hydroxylase/CYP7A1 in rat liver microsomes.{42274} 7α-hydroxy Cholesterol (40 µM) increases levels of the adhesion molecules ICAM-1, VCAM-1, and E-selectin in human umbilical vein endothelial cells (HUVECs).{60007} It increases secretion of chemokine (C-C motif) ligand 2 (CCL2) and matrix metalloproteinase-9 (MMP-9) in serum-deprived THP-1 cells when used at a concentration of 5 µg/ml.{42273} 7α-hydroxy Cholesterol has been found in macrophages isolated from atherosclerotic lesions in rabbits fed a high-cholesterol diet.{60008}  

     

    Brand:
    Cayman
    SKU:25547 - 1 mg

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  • 7α-hydroxy-4-Cholesten-3-one is a metabolite of 7α-hydroxy cholesterol and an intermediate in the biosynthesis of bile acids.{37690} Plasma levels of 7α-hydroxy-4-cholesten-3-one positively correlate with the rate of bile acid synthesis in humans and are increased in patients following ileal resection.{37691}  

     

    Brand:
    Cayman
    SKU:25442 - 1 mg

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  • GPR183 (also known as Epstein-Barr virus-induced gene 2) is an orphan G protein-coupled receptor (GPCR) that is highly expressed in spleen and is required for humoral immune responses, including B cell migration and T cell-dependent antibody production.{19918,19919} 7α,25-dihydroxy Cholesterol (7α,25-DHC) is a potent agonist of GPR183 that induces specific activation of the receptor with an EC50 value of 50 nM (Kd = 450 pM).{19918,19919} At concentrations below 3 μM, it does not show any appreciable binding activity when tested against eight different nuclear hormone receptors including LXR and thirty-one different G protein-coupled receptors in a panel of reporter gene assays.{19919} 7α,25-DHC can act as a potent chemokine, affecting migration of immune cells expressing GPR183 both in vitro (EC50 = 500 pM) and in vivo.{19918,19919}  

     

    Brand:
    Cayman
    SKU:11032 - 1 mg

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  • GPR183 (also known as Epstein-Barr virus-induced gene 2) is an orphan G protein-coupled receptor (GPCR) that is highly expressed in spleen and is required for humoral immune responses, including B cell migration and T cell-dependent antibody production.{19918,19919} 7α,25-dihydroxy Cholesterol (7α,25-DHC) is a potent agonist of GPR183 that induces specific activation of the receptor with an EC50 value of 50 nM (Kd = 450 pM).{19918,19919} At concentrations below 3 μM, it does not show any appreciable binding activity when tested against eight different nuclear hormone receptors including LXR and thirty-one different G protein-coupled receptors in a panel of reporter gene assays.{19919} 7α,25-DHC can act as a potent chemokine, affecting migration of immune cells expressing GPR183 both in vitro (EC50 = 500 pM) and in vivo.{19918,19919}  

     

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    Cayman
    SKU:11032 - 10 mg

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  • GPR183 (also known as Epstein-Barr virus-induced gene 2) is an orphan G protein-coupled receptor (GPCR) that is highly expressed in spleen and is required for humoral immune responses, including B cell migration and T cell-dependent antibody production.{19918,19919} 7α,25-dihydroxy Cholesterol (7α,25-DHC) is a potent agonist of GPR183 that induces specific activation of the receptor with an EC50 value of 50 nM (Kd = 450 pM).{19918,19919} At concentrations below 3 μM, it does not show any appreciable binding activity when tested against eight different nuclear hormone receptors including LXR and thirty-one different G protein-coupled receptors in a panel of reporter gene assays.{19919} 7α,25-DHC can act as a potent chemokine, affecting migration of immune cells expressing GPR183 both in vitro (EC50 = 500 pM) and in vivo.{19918,19919}  

     

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    Cayman
    SKU:11032 - 5 mg

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  • 7β-hydroxy Cholesterol is an oxysterol formed by enzymatic and non-enzymatic oxidation of cholesterol.{36765} It is the primary oxysterol found in LDL and induces apoptosis and cell death of human umbilical vein endothelial cells (HUVECs) in vitro in a concentration-dependent manner. Increased plasma levels of 7β-hydroxy cholesterol positively correlate with mortality in coronary heart disease in human males.{36766}  

     

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    Cayman
    SKU:20099 -

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  • 7β-hydroxy Cholesterol is an oxysterol formed by enzymatic and non-enzymatic oxidation of cholesterol.{36765} It is the primary oxysterol found in LDL and induces apoptosis and cell death of human umbilical vein endothelial cells (HUVECs) in vitro in a concentration-dependent manner. Increased plasma levels of 7β-hydroxy cholesterol positively correlate with mortality in coronary heart disease in human males.{36766}  

     

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    Cayman
    SKU:20099 -

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  • 7β-hydroxy Cholesterol-d7 is intended for use as an internal standard for the quantification of 7β-hydroxy cholesterol by GC- or LC-MS. 7β-hydroxy Cholesterol is an oxysterol formed by enzymatic and non-enzymatic oxidation of cholesterol.{36765} It is the primary oxysterol found in LDL and induces apoptosis and cell death of human umbilical vein endothelial cells (HUVECs) in vitro in a concentration-dependent manner. Increased plasma levels of 7β-hydroxy cholesterol positively correlate with mortality in coronary heart disease in human males.{36766}  

     

    Brand:
    Cayman
    SKU:25548 - 1 mg

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  • 7β-hydroxy Cholesterol-d7 is intended for use as an internal standard for the quantification of 7β-hydroxy cholesterol by GC- or LC-MS. 7β-hydroxy Cholesterol is an oxysterol formed by enzymatic and non-enzymatic oxidation of cholesterol.{36765} It is the primary oxysterol found in LDL and induces apoptosis and cell death of human umbilical vein endothelial cells (HUVECs) in vitro in a concentration-dependent manner. Increased plasma levels of 7β-hydroxy cholesterol positively correlate with mortality in coronary heart disease in human males.{36766}  

     

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    Cayman
    SKU:25548 - 500 µg

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  • 7β,27-dihydroxy Cholesterol is an oxysterol and agonist of retinoic acid receptor-related orphan receptor γ (RORγ) and RORγt.{33003} It activates RORγ- or RORγt-dependent signaling with EC50 values of 691 and 1,045 nM, respectively, in reporter assays using HEK293T cells expressing the recombinant human receptors. 7β,27-dihydroxy Cholesterol is selective for RORγ and RORγt over a panel of eight additional nuclear receptors at 30 µM. It increases IL-17A production in Th17-polarized isolated human naïve CD4+ T cells when used at a concentration of 300 nM. 7β,27-dihydroxy Cholesterol (60 mg/kg) increases IL-17A production in isolated mouse γδ T cells stimulated with 12-myristate 13-acetate (PMA; Item No. 10008014) and ionomycin (Item Nos. 10004974 | 11932).  

     

    Brand:
    Cayman
    SKU:20102 -

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  • 7β,27-dihydroxy Cholesterol is an oxysterol and agonist of retinoic acid receptor-related orphan receptor γ (RORγ) and RORγt.{33003} It activates RORγ- or RORγt-dependent signaling with EC50 values of 691 and 1,045 nM, respectively, in reporter assays using HEK293T cells expressing the recombinant human receptors. 7β,27-dihydroxy Cholesterol is selective for RORγ and RORγt over a panel of eight additional nuclear receptors at 30 µM. It increases IL-17A production in Th17-polarized isolated human naïve CD4+ T cells when used at a concentration of 300 nM. 7β,27-dihydroxy Cholesterol (60 mg/kg) increases IL-17A production in isolated mouse γδ T cells stimulated with 12-myristate 13-acetate (PMA; Item No. 10008014) and ionomycin (Item Nos. 10004974 | 11932).  

     

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    Cayman
    SKU:20102 -

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  • 8-(3-Chlorostyryl)caffeine (CSC) is an adenosine A2 receptor antagonist (Ki = 54 nM).{53268} It is selective for adenosine A2 over A1 receptors (Ki = 28 µM). CSC reverses locomotor depression induced by the adenosine A2A agonist APEC in mice (ED50 = 16 µg/kg, i.p.). It increases locomotion in mice when administered at a dose of 5 mg/kg. CSC (5 mg/kg) reverses the shortening of the rotational motor response and increases in striatal adenosine A2 receptor levels induced by L-DOPA (Item No. 13248) in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{53269} It also inhibits monoamine oxidase B (MAO-B; Ki = 100 nM) and reduces MAO-B activity in brain mitochondrial preparations from wild-type and A2A-/- mice.{53270}  

     

    Brand:
    Cayman
    SKU:29704 - 10 mg

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  • 8-(3-Chlorostyryl)caffeine (CSC) is an adenosine A2 receptor antagonist (Ki = 54 nM).{53268} It is selective for adenosine A2 over A1 receptors (Ki = 28 µM). CSC reverses locomotor depression induced by the adenosine A2A agonist APEC in mice (ED50 = 16 µg/kg, i.p.). It increases locomotion in mice when administered at a dose of 5 mg/kg. CSC (5 mg/kg) reverses the shortening of the rotational motor response and increases in striatal adenosine A2 receptor levels induced by L-DOPA (Item No. 13248) in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{53269} It also inhibits monoamine oxidase B (MAO-B; Ki = 100 nM) and reduces MAO-B activity in brain mitochondrial preparations from wild-type and A2A-/- mice.{53270}  

     

    Brand:
    Cayman
    SKU:29704 - 25 mg

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  • 8-(3-Chlorostyryl)caffeine (CSC) is an adenosine A2 receptor antagonist (Ki = 54 nM).{53268} It is selective for adenosine A2 over A1 receptors (Ki = 28 µM). CSC reverses locomotor depression induced by the adenosine A2A agonist APEC in mice (ED50 = 16 µg/kg, i.p.). It increases locomotion in mice when administered at a dose of 5 mg/kg. CSC (5 mg/kg) reverses the shortening of the rotational motor response and increases in striatal adenosine A2 receptor levels induced by L-DOPA (Item No. 13248) in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{53269} It also inhibits monoamine oxidase B (MAO-B; Ki = 100 nM) and reduces MAO-B activity in brain mitochondrial preparations from wild-type and A2A-/- mice.{53270}  

     

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    Cayman
    SKU:29704 - 50 mg

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  • 8-Aminoclonazolam (Item No. 27247) is an analytical reference standard categorized as a benzodiazepine metabolite.{40539} It is a metabolite of clonazolam. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:27247 - 1 mg

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  • 8-Aminoclonazolam (Item No. 27247) is an analytical reference standard categorized as a benzodiazepine metabolite.{40539} It is a metabolite of clonazolam. This product is intended for research and forensic applications.  

     

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    Cayman
    SKU:27247 - 5 mg

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  • 8-Aminopyrene-1,3,6-trisulfonic acid (APTS) is an anionic fluorescent dye with excitation/emission spectra of 425/503 nm, respectively.{37198} It forms a ground state complex with viologen-type quenchers, inducing a red-shift in the absorbance spectrum from 425 to 464 nm. APTS is pH insensitive, with the emission maximum remaining constant over the pH range of 4-10. It can be used in solution or immobilized through attachment of an aldehyde functionalized monomer by reductive amination without significantly changing fluorescence intensity. APTS has been used as a reporter for glucose sensing and for the detection of other saccharides.{37198,37199}  

     

    Brand:
    Cayman
    SKU:23098 - 1 mg

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  • 8-Aminopyrene-1,3,6-trisulfonic acid (APTS) is an anionic fluorescent dye with excitation/emission spectra of 425/503 nm, respectively.{37198} It forms a ground state complex with viologen-type quenchers, inducing a red-shift in the absorbance spectrum from 425 to 464 nm. APTS is pH insensitive, with the emission maximum remaining constant over the pH range of 4-10. It can be used in solution or immobilized through attachment of an aldehyde functionalized monomer by reductive amination without significantly changing fluorescence intensity. APTS has been used as a reporter for glucose sensing and for the detection of other saccharides.{37198,37199}  

     

    Brand:
    Cayman
    SKU:23098 - 10 mg

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  • 8-Aminopyrene-1,3,6-trisulfonic acid (APTS) is an anionic fluorescent dye with excitation/emission spectra of 425/503 nm, respectively.{37198} It forms a ground state complex with viologen-type quenchers, inducing a red-shift in the absorbance spectrum from 425 to 464 nm. APTS is pH insensitive, with the emission maximum remaining constant over the pH range of 4-10. It can be used in solution or immobilized through attachment of an aldehyde functionalized monomer by reductive amination without significantly changing fluorescence intensity. APTS has been used as a reporter for glucose sensing and for the detection of other saccharides.{37198,37199}  

     

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    Cayman
    SKU:23098 - 5 mg

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  • 8-bromo-Cyclic AMP is a brominated derivative of cAMP that remains long-acting due to its resistance to degradation by cAMP phosphodiesterase.{26217,26218} It can activate cAMP-dependent protein kinase, inhibiting growth, decreasing proliferation, increasing differentiation, and inducing apoptosis of cancer cells.{26218}  

     

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    Cayman
    SKU:-

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  • 8-bromo-Cyclic AMP is a brominated derivative of cAMP that remains long-acting due to its resistance to degradation by cAMP phosphodiesterase.{26217,26218} It can activate cAMP-dependent protein kinase, inhibiting growth, decreasing proliferation, increasing differentiation, and inducing apoptosis of cancer cells.{26218}  

     

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    Cayman
    SKU:-

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  • 8-bromo-Cyclic AMP is a brominated derivative of cAMP that remains long-acting due to its resistance to degradation by cAMP phosphodiesterase.{26217,26218} It can activate cAMP-dependent protein kinase, inhibiting growth, decreasing proliferation, increasing differentiation, and inducing apoptosis of cancer cells.{26218}  

     

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    Cayman
    SKU:-

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  • 8-bromo-Cyclic AMP is a brominated derivative of cAMP that remains long-acting due to its resistance to degradation by cAMP phosphodiesterase.{26217,26218} It can activate cAMP-dependent protein kinase, inhibiting growth, decreasing proliferation, increasing differentiation, and inducing apoptosis of cancer cells.{26218}  

     

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    Cayman
    SKU:-

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  • 8-bromo-Cyclic AMP (8-bromo-cAMP) is a cell-permeable analog of cAMP that activates cyclic-AMP-dependent protein kinase with a Ka value of 0.05 μM.{22886} It activates cyclic-GMP-dependent protein kinase with 100-fold reduced potency (Ka = 5.8 μM).{22886} 8-bromo-cAMP is more stable to hydrolysis and has increased membrane permeability compared to unmodified cAMP.{22886}  

     

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    Cayman
    SKU:-
  • 8-bromo-Cyclic AMP (8-bromo-cAMP) is a cell-permeable analog of cAMP that activates cyclic-AMP-dependent protein kinase with a Ka value of 0.05 μM.{22886} It activates cyclic-GMP-dependent protein kinase with 100-fold reduced potency (Ka = 5.8 μM).{22886} 8-bromo-cAMP is more stable to hydrolysis and has increased membrane permeability compared to unmodified cAMP.{22886}  

     

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    Cayman
    SKU:-
  • 8-bromo-Cyclic AMP (8-bromo-cAMP) is a cell-permeable analog of cAMP that activates cyclic-AMP-dependent protein kinase with a Ka value of 0.05 μM.{22886} It activates cyclic-GMP-dependent protein kinase with 100-fold reduced potency (Ka = 5.8 μM).{22886} 8-bromo-cAMP is more stable to hydrolysis and has increased membrane permeability compared to unmodified cAMP.{22886}  

     

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    Cayman
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  • 8-bromo-Cyclic GMP (8-bromo-cGMP) is a cell-permeable analog of cGMP that exhibits greater resistance to hydrolysis by phosphodiesterases than its parent compound. It preferentially activates cGMP-dependent protein kinase.{25938} At 1 µM-0.1 mM, 8-bromo-cGMP can inhibit acetylcholine-induced increases in intracellular calcium concentrations.{25937}  

     

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    Cayman
    SKU:-
  • 8-bromo-Cyclic GMP (8-bromo-cGMP) is a cell-permeable analog of cGMP that exhibits greater resistance to hydrolysis by phosphodiesterases than its parent compound. It preferentially activates cGMP-dependent protein kinase.{25938} At 1 µM-0.1 mM, 8-bromo-cGMP can inhibit acetylcholine-induced increases in intracellular calcium concentrations.{25937}  

     

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    Cayman
    SKU:-
  • 8-bromo-Cyclic GMP (8-bromo-cGMP) is a cell-permeable analog of cGMP that exhibits greater resistance to hydrolysis by phosphodiesterases than its parent compound. It preferentially activates cGMP-dependent protein kinase.{25938} At 1 µM-0.1 mM, 8-bromo-cGMP can inhibit acetylcholine-induced increases in intracellular calcium concentrations.{25937}  

     

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    Cayman
    SKU:-
  • 8-bromo-Cyclic GMP (8-bromo-cGMP) is a cell-permeable analog of cGMP that exhibits greater resistance to hydrolysis by phosphodiesterases than its parent compound. It preferentially activates cGMP-dependent protein kinase.{25938} At 1 µM-0.1 mM, 8-bromo-cGMP can inhibit acetylcholine-induced increases in intracellular calcium concentrations.{25937}  

     

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  • 8-Bromoguanosine is a brominated derivative of guanosine. Purine nucleobases with bromine at position eight are known to preferentially adopt the syn conformation as nucleosides and, thus, can be used to reduce the conformational heterogeneity of RNA to potentially enhance its function.{29473} It is reported to activate lymphocytes through an intracellular mechanism to exert immunostimulatory effects.{29472,29471}  

     

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    Cayman
    SKU:-

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  • 8-Bromoguanosine is a brominated derivative of guanosine. Purine nucleobases with bromine at position eight are known to preferentially adopt the syn conformation as nucleosides and, thus, can be used to reduce the conformational heterogeneity of RNA to potentially enhance its function.{29473} It is reported to activate lymphocytes through an intracellular mechanism to exert immunostimulatory effects.{29472,29471}  

     

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    Cayman
    SKU:-

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  • 8-Bromoguanosine is a brominated derivative of guanosine. Purine nucleobases with bromine at position eight are known to preferentially adopt the syn conformation as nucleosides and, thus, can be used to reduce the conformational heterogeneity of RNA to potentially enhance its function.{29473} It is reported to activate lymphocytes through an intracellular mechanism to exert immunostimulatory effects.{29472,29471}  

     

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    Cayman
    SKU:-

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  • 8-Bromoguanosine is a brominated derivative of guanosine. Purine nucleobases with bromine at position eight are known to preferentially adopt the syn conformation as nucleosides and, thus, can be used to reduce the conformational heterogeneity of RNA to potentially enhance its function.{29473} It is reported to activate lymphocytes through an intracellular mechanism to exert immunostimulatory effects.{29472,29471}  

     

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    Cayman
    SKU:-

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  • 8-Bromoisoquinoline is a synthetic intermediate useful for pharmaceutical synthesis.  

     

    Brand:
    Cayman
    SKU:10007082 - 1 g

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  • 8-Bromoisoquinoline is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    Cayman
    SKU:10007082 - 5 g

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  • 8-Bromoisoquinoline is a synthetic intermediate useful for pharmaceutical synthesis.  

     

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    Cayman
    SKU:10007082 - 500 mg

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  • 8-CPT-Cyclic AMP is a lipophilic activator of the cyclic-AMP- and cyclic-GMP-dependent protein kinases, PKA and PKG (Ka = 0.05 and 0.11 μM, respectively).{22886} 8-CPT-cAMP inhibits cyclic GMP-specific phosphodiesterase (PDE VA), cyclic GMP-inhibited phosphodiesterase (PDE III), and cyclic AMP-specific phosphodiesterase (PDE IV) with IC50 values of 0.9, 24, and 25 μM, respectively.{22887} It has been used in studies to analyze the signal transduction pathways initiated by cyclic-AMP- and cyclic-GMP-dependent protein kinases.  

     

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    Cayman
    SKU:12011 - 10 mg

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  • 8-CPT-Cyclic AMP is a lipophilic activator of the cyclic-AMP- and cyclic-GMP-dependent protein kinases, PKA and PKG (Ka = 0.05 and 0.11 μM, respectively).{22886} 8-CPT-cAMP inhibits cyclic GMP-specific phosphodiesterase (PDE VA), cyclic GMP-inhibited phosphodiesterase (PDE III), and cyclic AMP-specific phosphodiesterase (PDE IV) with IC50 values of 0.9, 24, and 25 μM, respectively.{22887} It has been used in studies to analyze the signal transduction pathways initiated by cyclic-AMP- and cyclic-GMP-dependent protein kinases.  

     

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    Cayman
    SKU:12011 - 25 mg

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  • 8-CPT-Cyclic AMP is a lipophilic activator of the cyclic-AMP- and cyclic-GMP-dependent protein kinases, PKA and PKG (Ka = 0.05 and 0.11 μM, respectively).{22886} 8-CPT-cAMP inhibits cyclic GMP-specific phosphodiesterase (PDE VA), cyclic GMP-inhibited phosphodiesterase (PDE III), and cyclic AMP-specific phosphodiesterase (PDE IV) with IC50 values of 0.9, 24, and 25 μM, respectively.{22887} It has been used in studies to analyze the signal transduction pathways initiated by cyclic-AMP- and cyclic-GMP-dependent protein kinases.  

     

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    Cayman
    SKU:12011 - 50 mg

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  • 8-Cyclopentyl-1,3-dimethylxanthine (CPT) is an adenosine A1 receptor antagonist (Ki = 10.9 nM).{48947} It is selective for adenosine A1 over A2 receptors (Ki = 1,440 nM). CPT inhibits hypoxia-induced depression of evoked synaptic potentials in rat hippocampal slices in a concentration-dependent manner.{48948} It increases secondary after-discharge duration in electrically induced seizures in rats when administered at doses of 2.5 mg/kg or higher.{48949} CPT increases the response rate under a fixed-interval schedule of stimulus-shock termination in squirrel monkeys (ED50 = 2.5 μmol/kg), indicating psychomotor stimulant effects.{48950}  

     

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    Cayman
    SKU:29870 - 100 mg

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  • 8-Cyclopentyl-1,3-dimethylxanthine (CPT) is an adenosine A1 receptor antagonist (Ki = 10.9 nM).{48947} It is selective for adenosine A1 over A2 receptors (Ki = 1,440 nM). CPT inhibits hypoxia-induced depression of evoked synaptic potentials in rat hippocampal slices in a concentration-dependent manner.{48948} It increases secondary after-discharge duration in electrically induced seizures in rats when administered at doses of 2.5 mg/kg or higher.{48949} CPT increases the response rate under a fixed-interval schedule of stimulus-shock termination in squirrel monkeys (ED50 = 2.5 μmol/kg), indicating psychomotor stimulant effects.{48950}  

     

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    Cayman
    SKU:29870 - 250 mg

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  • 8-Cyclopentyl-1,3-dimethylxanthine (CPT) is an adenosine A1 receptor antagonist (Ki = 10.9 nM).{48947} It is selective for adenosine A1 over A2 receptors (Ki = 1,440 nM). CPT inhibits hypoxia-induced depression of evoked synaptic potentials in rat hippocampal slices in a concentration-dependent manner.{48948} It increases secondary after-discharge duration in electrically induced seizures in rats when administered at doses of 2.5 mg/kg or higher.{48949} CPT increases the response rate under a fixed-interval schedule of stimulus-shock termination in squirrel monkeys (ED50 = 2.5 μmol/kg), indicating psychomotor stimulant effects.{48950}  

     

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    Cayman
    SKU:29870 - 50 mg

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  • 8-dehydro Cholesterol (8-DHC) is an isomer of the cholesterol precursor 7-DHC (Item No. 14612).{36903,36904,35287} It accumulates in tissues and plasma in patients with Smith-Lemli-Opitz syndrome (SLOS), a disorder characterized by a mutation in DHCR7, the gene encoding 3β-hydroxysterol-Δ7-reductase, and decreased cholesterol levels in bodily tissues and fluids, as well as microcephaly, intellectual disability, and distinctive dysmorphic features. 8-DHC levels are increased in serum in a rat model of SLOS induced by the DHCR7 inhibitor AY 9944 (Item No. 14611).{36903}  

     

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    Cayman
    SKU:25970 - 1 mg

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  • 8-dehydro Cholesterol (8-DHC) is an isomer of the cholesterol precursor 7-DHC (Item No. 14612).{36903,36904,35287} It accumulates in tissues and plasma in patients with Smith-Lemli-Opitz syndrome (SLOS), a disorder characterized by a mutation in DHCR7, the gene encoding 3β-hydroxysterol-Δ7-reductase, and decreased cholesterol levels in bodily tissues and fluids, as well as microcephaly, intellectual disability, and distinctive dysmorphic features. 8-DHC levels are increased in serum in a rat model of SLOS induced by the DHCR7 inhibitor AY 9944 (Item No. 14611).{36903}  

     

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    Cayman
    SKU:25970 - 10 mg

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  • 8-dehydro Cholesterol (8-DHC) is an isomer of the cholesterol precursor 7-DHC (Item No. 14612).{36903,36904,35287} It accumulates in tissues and plasma in patients with Smith-Lemli-Opitz syndrome (SLOS), a disorder characterized by a mutation in DHCR7, the gene encoding 3β-hydroxysterol-Δ7-reductase, and decreased cholesterol levels in bodily tissues and fluids, as well as microcephaly, intellectual disability, and distinctive dysmorphic features. 8-DHC levels are increased in serum in a rat model of SLOS induced by the DHCR7 inhibitor AY 9944 (Item No. 14611).{36903}  

     

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    Cayman
    SKU:25970 - 5 mg

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  • 8-Gingerol is a natural chemical found in the rhizomes of ginger (Z. officinale). It contains the same aromatic region and polar link but has a longer hydrophobic tail than the more abundant 6-gingerol (Item No. 11707). Like 6-gingerol, 8-gingerol activates the transient receptor potential vanilloid receptor 1 (TRPV1; EC50 = 5.0 µM), inhibits COX-2, and inhibits the growth of H. pylori in vitro.{32701,25924} 8-Gingerol also augments wound healing, suppresses IL-2-induced proliferation of T lymphocytes, and potentiates β-agonist-induced relaxation of airway smooth muscle.{32699,32700,32704} Oral 8-gingerol is expected to be readily absorbed and rapidly metabolized by glucuronidation and sulfation, with minimal to modest effects on cytochrome P450 isoforms.{32702,32703}  

     

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    Cayman
    SKU:11841 - 1 mg

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  • 8-Gingerol is a natural chemical found in the rhizomes of ginger (Z. officinale). It contains the same aromatic region and polar link but has a longer hydrophobic tail than the more abundant 6-gingerol (Item No. 11707). Like 6-gingerol, 8-gingerol activates the transient receptor potential vanilloid receptor 1 (TRPV1; EC50 = 5.0 µM), inhibits COX-2, and inhibits the growth of H. pylori in vitro.{32701,25924} 8-Gingerol also augments wound healing, suppresses IL-2-induced proliferation of T lymphocytes, and potentiates β-agonist-induced relaxation of airway smooth muscle.{32699,32700,32704} Oral 8-gingerol is expected to be readily absorbed and rapidly metabolized by glucuronidation and sulfation, with minimal to modest effects on cytochrome P450 isoforms.{32702,32703}  

     

    Brand:
    Cayman
    SKU:11841 - 10 mg

    Available on backorder

  • 8-Gingerol is a natural chemical found in the rhizomes of ginger (Z. officinale). It contains the same aromatic region and polar link but has a longer hydrophobic tail than the more abundant 6-gingerol (Item No. 11707). Like 6-gingerol, 8-gingerol activates the transient receptor potential vanilloid receptor 1 (TRPV1; EC50 = 5.0 µM), inhibits COX-2, and inhibits the growth of H. pylori in vitro.{32701,25924} 8-Gingerol also augments wound healing, suppresses IL-2-induced proliferation of T lymphocytes, and potentiates β-agonist-induced relaxation of airway smooth muscle.{32699,32700,32704} Oral 8-gingerol is expected to be readily absorbed and rapidly metabolized by glucuronidation and sulfation, with minimal to modest effects on cytochrome P450 isoforms.{32702,32703}  

     

    Brand:
    Cayman
    SKU:11841 - 25 mg

    Available on backorder

  • 8-Gingerol is a natural chemical found in the rhizomes of ginger (Z. officinale). It contains the same aromatic region and polar link but has a longer hydrophobic tail than the more abundant 6-gingerol (Item No. 11707). Like 6-gingerol, 8-gingerol activates the transient receptor potential vanilloid receptor 1 (TRPV1; EC50 = 5.0 µM), inhibits COX-2, and inhibits the growth of H. pylori in vitro.{32701,25924} 8-Gingerol also augments wound healing, suppresses IL-2-induced proliferation of T lymphocytes, and potentiates β-agonist-induced relaxation of airway smooth muscle.{32699,32700,32704} Oral 8-gingerol is expected to be readily absorbed and rapidly metabolized by glucuronidation and sulfation, with minimal to modest effects on cytochrome P450 isoforms.{32702,32703}  

     

    Brand:
    Cayman
    SKU:11841 - 5 mg

    Available on backorder

  • 8-Hydroxy DPAT (8-OH-DPAT) is an agonist of serotonin (5-HT) receptor subtype 5-HT1A (EC50 = 12 nM in rat hippocampal membranes).{40744} It mimics the effect of serotonin (Item No. 14332) on reducing excitatory post-synaptic potentials (EPSPs) in the entorhinal cortex layers II and III when used at concentrations of 10 and 50 µM.{40748} In rhesus monkeys, it enhances the behavioral effects of Δ9-tetrahydrocannabinol (Δ9-THC; Item Nos. 12068 | ISO60157) in a discriminant stimulus-shock test when administered at a dose of 0.178 mg/kg.{40743} In mice, 8-OH-DPAT reduces the number of attack bites when administered directly to the dorsal raphe nucleus in a baclofen-induced model of aggressiveness and impairs contextual fear when administered prior to training at a dose of 0.5 mg/kg.{40747,40746} It also reduces the incidence of apnea and improves respiratory regularity in a methyl-CpG-binding protein 2-deficient mouse model of Rett syndrome when administered at a dose of 50 µg/kg.{40742} In a rat model of diabetes, 8-OH-DPAT enhances bradycardia in response to vagal electrical stimulation.{40745}  

     

    Brand:
    Cayman
    SKU:22608 -

    Out of stock

  • 8-Hydroxy DPAT (8-OH-DPAT) is an agonist of serotonin (5-HT) receptor subtype 5-HT1A (EC50 = 12 nM in rat hippocampal membranes).{40744} It mimics the effect of serotonin (Item No. 14332) on reducing excitatory post-synaptic potentials (EPSPs) in the entorhinal cortex layers II and III when used at concentrations of 10 and 50 µM.{40748} In rhesus monkeys, it enhances the behavioral effects of Δ9-tetrahydrocannabinol (Δ9-THC; Item Nos. 12068 | ISO60157) in a discriminant stimulus-shock test when administered at a dose of 0.178 mg/kg.{40743} In mice, 8-OH-DPAT reduces the number of attack bites when administered directly to the dorsal raphe nucleus in a baclofen-induced model of aggressiveness and impairs contextual fear when administered prior to training at a dose of 0.5 mg/kg.{40747,40746} It also reduces the incidence of apnea and improves respiratory regularity in a methyl-CpG-binding protein 2-deficient mouse model of Rett syndrome when administered at a dose of 50 µg/kg.{40742} In a rat model of diabetes, 8-OH-DPAT enhances bradycardia in response to vagal electrical stimulation.{40745}  

     

    Brand:
    Cayman
    SKU:22608 -

    Out of stock

  • 8-Hydroxy DPAT (8-OH-DPAT) is an agonist of serotonin (5-HT) receptor subtype 5-HT1A (EC50 = 12 nM in rat hippocampal membranes).{40744} It mimics the effect of serotonin (Item No. 14332) on reducing excitatory post-synaptic potentials (EPSPs) in the entorhinal cortex layers II and III when used at concentrations of 10 and 50 µM.{40748} In rhesus monkeys, it enhances the behavioral effects of Δ9-tetrahydrocannabinol (Δ9-THC; Item Nos. 12068 | ISO60157) in a discriminant stimulus-shock test when administered at a dose of 0.178 mg/kg.{40743} In mice, 8-OH-DPAT reduces the number of attack bites when administered directly to the dorsal raphe nucleus in a baclofen-induced model of aggressiveness and impairs contextual fear when administered prior to training at a dose of 0.5 mg/kg.{40747,40746} It also reduces the incidence of apnea and improves respiratory regularity in a methyl-CpG-binding protein 2-deficient mouse model of Rett syndrome when administered at a dose of 50 µg/kg.{40742} In a rat model of diabetes, 8-OH-DPAT enhances bradycardia in response to vagal electrical stimulation.{40745}  

     

    Brand:
    Cayman
    SKU:22608 -

    Out of stock

  • 8-hydroxy Efavirenz is a major oxidative metabolite of the non-nucleoside reverse transcriptase inhibitor efavirenz (Item No. 14412).{49116} 8-hydroxy Efavirenz is formed when efavirenz is metabolized by the cytochrome P450 (CYP) isoform CYP2B6. It induces apoptosis in rat primary hippocampal neurons and loss of dendritic spines in rat primary hippocampal neuronal cultures when used at a concentration of 0.01 μM.{49117}  

     

    Brand:
    Cayman
    SKU:27853 - 1 mg

    Available on backorder