Cayman

Showing 3001–3150 of 45550 results

  • 10-methyl-9-(phenoxycarbonyl) Acridinium is an acridinium ester that produces fluorescent 10-methyl-9-acridone upon oxidation with hydrogen peroxide, persulfates, and other oxidants in alkaline conditions.{48019,48020} Acridinium salts, including 10-methyl-9-(phenoxycarbonyl) acridinium, can be used in chemiluminescence assays, enzyme, antigen, antibody, and hormone immunoassays, and assays to detect oxidants in environmental, biological, and pharmaceutical samples.{48019,48020,48021}  

     

    Brand:
    Cayman
    SKU:25885 - 25 mg

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  • 10-methyl-9-(phenoxycarbonyl) Acridinium is an acridinium ester that produces fluorescent 10-methyl-9-acridone upon oxidation with hydrogen peroxide, persulfates, and other oxidants in alkaline conditions.{48019,48020} Acridinium salts, including 10-methyl-9-(phenoxycarbonyl) acridinium, can be used in chemiluminescence assays, enzyme, antigen, antibody, and hormone immunoassays, and assays to detect oxidants in environmental, biological, and pharmaceutical samples.{48019,48020,48021}  

     

    Brand:
    Cayman
    SKU:25885 - 5 mg

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  • 10-methyl-9-(phenoxycarbonyl) Acridinium is an acridinium ester that produces fluorescent 10-methyl-9-acridone upon oxidation with hydrogen peroxide, persulfates, and other oxidants in alkaline conditions.{48019,48020} Acridinium salts, including 10-methyl-9-(phenoxycarbonyl) acridinium, can be used in chemiluminescence assays, enzyme, antigen, antibody, and hormone immunoassays, and assays to detect oxidants in environmental, biological, and pharmaceutical samples.{48019,48020,48021}  

     

    Brand:
    Cayman
    SKU:25885 - 50 mg

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  • 10-Methyldodec-2-en-4-olide is a volatile lactone that has been found in Streptomyces.{42955,42956} It is active against the plant pathogenic fungus B. cinerea, the yeast S. cerevisiae, and the bacteria S. aureus, M. luteus, and M. phlei in an agar diffusion inhibition assay when used at a concentration of 140 μg per disc.{42957} 10-Methyldodec-2-en-4-olide also inhibits induction of a GFP-based reporter by the quorum sensing molecule N-dodecanoylhomoserine lactone (Item No. 10011203) in an N-acylhomoserine lactone (AHL) P. putida biosensor strain.  

     

    Brand:
    Cayman
    SKU:28407 - 1 mg

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  • 10-Nitrolinoleate is the product of nitration of linoleate by NO-derived reactive species.{25769,11912} Other nitrolinoleates detected in human plasma and urine include 9-, 12-, and 13-nitrolinoleate.{25770} Nitrolinoleates activate peroxisome proliferator-activated receptor γ (PPARγ; Ki = 133 nM), inducing CD36 expression in macrophages, adipocyte differentiation, and glucose uptake.{14255,13284} Nitrolinoleates can also be metabolized by smooth muscle cells to produce nitrite derivatives which in turn form NO, leading to increased cGMP production and smooth muscle relaxation.{11912,13287} Through the same mechanism, nitrolinoleate-derived NO suppresses leukocyte adhesion, in part through nitrosation of CD40.{25768} Alteratively, nitrolinoleates can act independently of NO/cGMP and PPARγ signaling to suppress neutrophil and macrophage functions.{25769,25770,14473}  

     

    Brand:
    Cayman
    SKU:10037 - 1 mg

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  • 10-Nitrolinoleate is the product of nitration of linoleate by NO-derived reactive species.{25769,11912} Other nitrolinoleates detected in human plasma and urine include 9-, 12-, and 13-nitrolinoleate.{25770} Nitrolinoleates activate peroxisome proliferator-activated receptor γ (PPARγ; Ki = 133 nM), inducing CD36 expression in macrophages, adipocyte differentiation, and glucose uptake.{14255,13284} Nitrolinoleates can also be metabolized by smooth muscle cells to produce nitrite derivatives which in turn form NO, leading to increased cGMP production and smooth muscle relaxation.{11912,13287} Through the same mechanism, nitrolinoleate-derived NO suppresses leukocyte adhesion, in part through nitrosation of CD40.{25768} Alteratively, nitrolinoleates can act independently of NO/cGMP and PPARγ signaling to suppress neutrophil and macrophage functions.{25769,25770,14473}  

     

    Brand:
    Cayman
    SKU:10037 - 100 µg

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  • 10-Nitrolinoleate is the product of nitration of linoleate by NO-derived reactive species.{25769,11912} Other nitrolinoleates detected in human plasma and urine include 9-, 12-, and 13-nitrolinoleate.{25770} Nitrolinoleates activate peroxisome proliferator-activated receptor γ (PPARγ; Ki = 133 nM), inducing CD36 expression in macrophages, adipocyte differentiation, and glucose uptake.{14255,13284} Nitrolinoleates can also be metabolized by smooth muscle cells to produce nitrite derivatives which in turn form NO, leading to increased cGMP production and smooth muscle relaxation.{11912,13287} Through the same mechanism, nitrolinoleate-derived NO suppresses leukocyte adhesion, in part through nitrosation of CD40.{25768} Alteratively, nitrolinoleates can act independently of NO/cGMP and PPARγ signaling to suppress neutrophil and macrophage functions.{25769,25770,14473}  

     

    Brand:
    Cayman
    SKU:10037 - 500 µg

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  • Nitrated unsaturated fatty acids, such as 10- and 12-nitrolinoleate (LNO2; Item No. 10037), cholesteryl nitrolinoleate, and nitrohydroxylinoleate, represent a new class of endogenous lipid-derived signalling molecules. LNO2 isomers serve as potent endogenous ligands for PPARγ and can also decompose or be metabolized to release nitric oxide.{11912,13284,13287,13288} 10-Nitrooleate is one of two regioisomers of nitrooleate, the other being 9-nitrooleate (Item No. 10008042) (OA-NO2; used for the mixture of isomers), which are formed by nitration of oleic acid in approximately equal proportions in vivo.{14255} Peroxynitrite, acidified nitrite, and myeloperoxidase in the presence of H2O2 and nitrite, all mediate the nitration of oleic acid. OA-NO2 is found in human plasma as the free acid and esterified in phospholipids at concentrations of 619 ± 52 nM and 302 ± 369 nM, respectively. OA-NO2 activates PPARγ approximately 7-fold at a concentration of 1 µM and effectively promotes differentiation 3T3-L1 preadipocytes to adipocytes at 3 µM.{14255}  

     

    Brand:
    Cayman
    SKU:10008043 - 1 mg

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  • Nitrated unsaturated fatty acids, such as 10- and 12-nitrolinoleate (LNO2; Item No. 10037), cholesteryl nitrolinoleate, and nitrohydroxylinoleate, represent a new class of endogenous lipid-derived signalling molecules. LNO2 isomers serve as potent endogenous ligands for PPARγ and can also decompose or be metabolized to release nitric oxide.{11912,13284,13287,13288} 10-Nitrooleate is one of two regioisomers of nitrooleate, the other being 9-nitrooleate (Item No. 10008042) (OA-NO2; used for the mixture of isomers), which are formed by nitration of oleic acid in approximately equal proportions in vivo.{14255} Peroxynitrite, acidified nitrite, and myeloperoxidase in the presence of H2O2 and nitrite, all mediate the nitration of oleic acid. OA-NO2 is found in human plasma as the free acid and esterified in phospholipids at concentrations of 619 ± 52 nM and 302 ± 369 nM, respectively. OA-NO2 activates PPARγ approximately 7-fold at a concentration of 1 µM and effectively promotes differentiation 3T3-L1 preadipocytes to adipocytes at 3 µM.{14255}  

     

    Brand:
    Cayman
    SKU:10008043 - 100 µg

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  • Nitrated unsaturated fatty acids, such as 10- and 12-nitrolinoleate (LNO2; Item No. 10037), cholesteryl nitrolinoleate, and nitrohydroxylinoleate, represent a new class of endogenous lipid-derived signalling molecules. LNO2 isomers serve as potent endogenous ligands for PPARγ and can also decompose or be metabolized to release nitric oxide.{11912,13284,13287,13288} 10-Nitrooleate is one of two regioisomers of nitrooleate, the other being 9-nitrooleate (Item No. 10008042) (OA-NO2; used for the mixture of isomers), which are formed by nitration of oleic acid in approximately equal proportions in vivo.{14255} Peroxynitrite, acidified nitrite, and myeloperoxidase in the presence of H2O2 and nitrite, all mediate the nitration of oleic acid. OA-NO2 is found in human plasma as the free acid and esterified in phospholipids at concentrations of 619 ± 52 nM and 302 ± 369 nM, respectively. OA-NO2 activates PPARγ approximately 7-fold at a concentration of 1 µM and effectively promotes differentiation 3T3-L1 preadipocytes to adipocytes at 3 µM.{14255}  

     

    Brand:
    Cayman
    SKU:10008043 - 50 µg

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  • Nitrated unsaturated fatty acids, such as 10- and 12-nitrolinoleate (LNO2; Item No. 10037), cholesteryl nitrolinoleate, and nitrohydroxylinoleate, represent a new class of endogenous lipid-derived signalling molecules. LNO2 isomers serve as potent endogenous ligands for PPARγ and can also decompose or be metabolized to release nitric oxide.{11912,13284,13287,13288} 10-Nitrooleate is one of two regioisomers of nitrooleate, the other being 9-nitrooleate (Item No. 10008042) (OA-NO2; used for the mixture of isomers), which are formed by nitration of oleic acid in approximately equal proportions in vivo.{14255} Peroxynitrite, acidified nitrite, and myeloperoxidase in the presence of H2O2 and nitrite, all mediate the nitration of oleic acid. OA-NO2 is found in human plasma as the free acid and esterified in phospholipids at concentrations of 619 ± 52 nM and 302 ± 369 nM, respectively. OA-NO2 activates PPARγ approximately 7-fold at a concentration of 1 µM and effectively promotes differentiation 3T3-L1 preadipocytes to adipocytes at 3 µM.{14255}  

     

    Brand:
    Cayman
    SKU:10008043 - 500 µg

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  • 10-Norparvulenone is a fungal metabolite originally isolated from Microsphaeropsis.{49592} It decreases viral sialidase activity in, and increases survival of, MDCK cells infected with the mouse-adapted influenza virus A/PR/8/34 when used at a concentration of 1 µg/ml.  

     

    Brand:
    Cayman
    SKU:29452 - 1 mg

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  • 10-oxo Docetaxel is a degradation product of docetaxel (Item No. 11637).{56040}  

     

    Brand:
    Cayman
    SKU:21672 -

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  • 10-oxo Docetaxel is a degradation product of docetaxel (Item No. 11637).{56040}  

     

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    Cayman
    SKU:21672 -

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  • 10-PAHSA is a newly identified endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs). It is a FAHFA in which palmitic acid (Item No. 10006627) is esterified to 10-hydroxy stearic acid. Among the FAHFA family members, PAHSAs are the most abundant in the adipose tissue of glucose tolerant AG4OX mice, which overexpress the Glut4 glucose transporter specifically in adipose tissue.{27644} As other FAHFAs improve glucose tolerance, stimulate insulin secretion, and have anti-inflammatory effects, 10-PAHSA may be a bioactive lipid with roles in metabolic syndrome and inflammation.{27644}  

     

    Brand:
    Cayman
    SKU:19973 -

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  • 10-PAHSA is a newly identified endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs). It is a FAHFA in which palmitic acid (Item No. 10006627) is esterified to 10-hydroxy stearic acid. Among the FAHFA family members, PAHSAs are the most abundant in the adipose tissue of glucose tolerant AG4OX mice, which overexpress the Glut4 glucose transporter specifically in adipose tissue.{27644} As other FAHFAs improve glucose tolerance, stimulate insulin secretion, and have anti-inflammatory effects, 10-PAHSA may be a bioactive lipid with roles in metabolic syndrome and inflammation.{27644}  

     

    Brand:
    Cayman
    SKU:19973 -

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  • 10-PAHSA is a newly identified endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs). It is a FAHFA in which palmitic acid (Item No. 10006627) is esterified to 10-hydroxy stearic acid. Among the FAHFA family members, PAHSAs are the most abundant in the adipose tissue of glucose tolerant AG4OX mice, which overexpress the Glut4 glucose transporter specifically in adipose tissue.{27644} As other FAHFAs improve glucose tolerance, stimulate insulin secretion, and have anti-inflammatory effects, 10-PAHSA may be a bioactive lipid with roles in metabolic syndrome and inflammation.{27644}  

     

    Brand:
    Cayman
    SKU:19973 -

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  • 10-Pyrene-PC is a substrate for all PLA2s with the exception of cPLA2 and PAF-AH.{5681} Upon phospholipid hydrolysis, 10-pyrenyldecanoic acid is produced from 10-pyrene-PC. The monomeric 10-pyrenyldecanoic acid exhibits fluorescence (excitation 345 nm, emission 395 nm), allowing quantitation of phospholipase activity.{3839}  

     

    Brand:
    Cayman
    SKU:62245 - 1 mg

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  • 10-Pyrene-PC is a substrate for all PLA2s with the exception of cPLA2 and PAF-AH.{5681} Upon phospholipid hydrolysis, 10-pyrenyldecanoic acid is produced from 10-pyrene-PC. The monomeric 10-pyrenyldecanoic acid exhibits fluorescence (excitation 345 nm, emission 395 nm), allowing quantitation of phospholipase activity.{3839}  

     

    Brand:
    Cayman
    SKU:62245 - 10 mg

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  • 10-Pyrene-PC is a substrate for all PLA2s with the exception of cPLA2 and PAF-AH.{5681} Upon phospholipid hydrolysis, 10-pyrenyldecanoic acid is produced from 10-pyrene-PC. The monomeric 10-pyrenyldecanoic acid exhibits fluorescence (excitation 345 nm, emission 395 nm), allowing quantitation of phospholipase activity.{3839}  

     

    Brand:
    Cayman
    SKU:62245 - 5 mg

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  • Heteroatom-substituted fatty acids have been observed to modulate the extension and desaturating of fatty acids, and to influence their distribution within phospholipids pools.{13246,13251} 10-Thiastearic acid inhibits desaturation of radiolabeled stearate to oleate in rat hepatocytes and hepatoma cells by more than 80% at a concentration of 25 µM.{13250} This activity is associated with a hypolipidemic effect, making this 10-thiastearic acid a useful tool for evaluating new anti-obesity therapeutics.  

     

    Brand:
    Cayman
    SKU:10007417 - 10 mg

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  • Heteroatom-substituted fatty acids have been observed to modulate the extension and desaturating of fatty acids, and to influence their distribution within phospholipids pools.{13246,13251} 10-Thiastearic acid inhibits desaturation of radiolabeled stearate to oleate in rat hepatocytes and hepatoma cells by more than 80% at a concentration of 25 µM.{13250} This activity is associated with a hypolipidemic effect, making this 10-thiastearic acid a useful tool for evaluating new anti-obesity therapeutics.  

     

    Brand:
    Cayman
    SKU:10007417 - 100 mg

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  • Heteroatom-substituted fatty acids have been observed to modulate the extension and desaturating of fatty acids, and to influence their distribution within phospholipids pools.{13246,13251} 10-Thiastearic acid inhibits desaturation of radiolabeled stearate to oleate in rat hepatocytes and hepatoma cells by more than 80% at a concentration of 25 µM.{13250} This activity is associated with a hypolipidemic effect, making this 10-thiastearic acid a useful tool for evaluating new anti-obesity therapeutics.  

     

    Brand:
    Cayman
    SKU:10007417 - 5 mg

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  • Heteroatom-substituted fatty acids have been observed to modulate the extension and desaturating of fatty acids, and to influence their distribution within phospholipids pools.{13246,13251} 10-Thiastearic acid inhibits desaturation of radiolabeled stearate to oleate in rat hepatocytes and hepatoma cells by more than 80% at a concentration of 25 µM.{13250} This activity is associated with a hypolipidemic effect, making this 10-thiastearic acid a useful tool for evaluating new anti-obesity therapeutics.  

     

    Brand:
    Cayman
    SKU:10007417 - 50 mg

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  • 10,11-dehydro Curvularin is a natural mycotoxin that has cytotoxic activity against select cancer cell lines.{34313,34316} It has been shown to activate the heat shock response, block TGF-β signaling, and scavenge superoxide anions.{34313,34314,34315}  

     

    Brand:
    Cayman
    SKU:21801 -

    Out of stock

  • 10,11-dehydro Curvularin is a natural mycotoxin that has cytotoxic activity against select cancer cell lines.{34313,34316} It has been shown to activate the heat shock response, block TGF-β signaling, and scavenge superoxide anions.{34313,34314,34315}  

     

    Brand:
    Cayman
    SKU:21801 -

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  • 10,11-dehydro Curvularin is a natural mycotoxin that has cytotoxic activity against select cancer cell lines.{34313,34316} It has been shown to activate the heat shock response, block TGF-β signaling, and scavenge superoxide anions.{34313,34314,34315}  

     

    Brand:
    Cayman
    SKU:21801 -

    Out of stock

  • 10,11-dihydro-10-hydroxy Carbamazepinee is the active metabolite of oxcarbazepine (Item No. 17340). Oxcarbazepine is rapidly and almost completely converted to 10,11-dihydro-10-hydroxycarbamazepine, which then demonstrates anticonvulsant efficacy by modulating several ion channels and receptors.{25311,25313} 10,11-dihydro-10-hydroxy Carbamazepine is reported to inhibit both voltage-gated Na+ and Ca2+ channels, to potentiate voltage-gated K+ channels, to antagonize adenosine A1 receptors, to increase dopaminergic transmission, and to inhibit glutamate release.{25311}  

     

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    Cayman
    SKU:-

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  • 10,11-dihydro-10-hydroxy Carbamazepinee is the active metabolite of oxcarbazepine (Item No. 17340). Oxcarbazepine is rapidly and almost completely converted to 10,11-dihydro-10-hydroxycarbamazepine, which then demonstrates anticonvulsant efficacy by modulating several ion channels and receptors.{25311,25313} 10,11-dihydro-10-hydroxy Carbamazepine is reported to inhibit both voltage-gated Na+ and Ca2+ channels, to potentiate voltage-gated K+ channels, to antagonize adenosine A1 receptors, to increase dopaminergic transmission, and to inhibit glutamate release.{25311}  

     

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    Cayman
    SKU:-

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  • 10,11-dihydro-10-hydroxy Carbamazepinee is the active metabolite of oxcarbazepine (Item No. 17340). Oxcarbazepine is rapidly and almost completely converted to 10,11-dihydro-10-hydroxycarbamazepine, which then demonstrates anticonvulsant efficacy by modulating several ion channels and receptors.{25311,25313} 10,11-dihydro-10-hydroxy Carbamazepine is reported to inhibit both voltage-gated Na+ and Ca2+ channels, to potentiate voltage-gated K+ channels, to antagonize adenosine A1 receptors, to increase dopaminergic transmission, and to inhibit glutamate release.{25311}  

     

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    Cayman
    SKU:-

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  • 10,11-dihydro-10-hydroxy Carbamazepinee is the active metabolite of oxcarbazepine (Item No. 17340). Oxcarbazepine is rapidly and almost completely converted to 10,11-dihydro-10-hydroxycarbamazepine, which then demonstrates anticonvulsant efficacy by modulating several ion channels and receptors.{25311,25313} 10,11-dihydro-10-hydroxy Carbamazepine is reported to inhibit both voltage-gated Na+ and Ca2+ channels, to potentiate voltage-gated K+ channels, to antagonize adenosine A1 receptors, to increase dopaminergic transmission, and to inhibit glutamate release.{25311}  

     

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    Cayman
    SKU:-

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  • 10,13-epoxy-10,12-Octadecadienoic acid is a furan fatty acid produced by oxidation of 10(E),12(Z)-conjugated linoleic acid (Item No. 90145).{46131,46132} It upregulates the expression of PLIN2, TPD52L2, and SEC13, which are involved in the formation of lipid droplets, and downregulates a variety of genes involved in general cellular processes in Caco-2 cells.{46132} 10,13-epoxy-10,12-Octadecadienoic acid is cytotoxic to Caco-2 and HepG2 cells when used concentrations greater than or equal to 100 µM.  

     

    Brand:
    Cayman
    SKU:26767 - 1 mg

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  • 10,13-epoxy-10,12-Octadecadienoic acid is a furan fatty acid produced by oxidation of 10(E),12(Z)-conjugated linoleic acid (Item No. 90145).{46131,46132} It upregulates the expression of PLIN2, TPD52L2, and SEC13, which are involved in the formation of lipid droplets, and downregulates a variety of genes involved in general cellular processes in Caco-2 cells.{46132} 10,13-epoxy-10,12-Octadecadienoic acid is cytotoxic to Caco-2 and HepG2 cells when used concentrations greater than or equal to 100 µM.  

     

    Brand:
    Cayman
    SKU:26767 - 500 µg

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  • 10’-Desmethoxystreptonigrin is an antibiotic originally isolated from Streptomyces and a derivative of the antibiotic streptonigrin.{49160} It is active against a variety of bacteria, including S. aureus, S. faecalis, E. coli, K. pneumoniae, and P. vulgaris (MICs = 0.4, 1.6, 3.1, 3.1, and 0.4 µg/ml, respectively).{49161} 10’-Desmethoxystreptonigrin is cytotoxic to HCT116 colon and A2780 ovarian cancer cells (IC50s = 0.004 and 0.001 µg/ml, respectively), as well as HCT116 cells resistant to etoposide (Item No. 12092) and teniposide (Item No. 14425) and cisplatin-resistant A2780 cells (IC50s = 0.003, 0.001, and 0.01 µg/ml, respectively). 10’-Desmethoxystreptonigrin is also an inhibitor of p21ras farnesylation (IC50 = 21 nM).  

     

    Brand:
    Cayman
    SKU:28065 - 2.5 mg

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  • 10’-Desmethoxystreptonigrin is an antibiotic originally isolated from Streptomyces and a derivative of the antibiotic streptonigrin.{49160} It is active against a variety of bacteria, including S. aureus, S. faecalis, E. coli, K. pneumoniae, and P. vulgaris (MICs = 0.4, 1.6, 3.1, 3.1, and 0.4 µg/ml, respectively).{49161} 10’-Desmethoxystreptonigrin is cytotoxic to HCT116 colon and A2780 ovarian cancer cells (IC50s = 0.004 and 0.001 µg/ml, respectively), as well as HCT116 cells resistant to etoposide (Item No. 12092) and teniposide (Item No. 14425) and cisplatin-resistant A2780 cells (IC50s = 0.003, 0.001, and 0.01 µg/ml, respectively). 10’-Desmethoxystreptonigrin is also an inhibitor of p21ras farnesylation (IC50 = 21 nM).  

     

    Brand:
    Cayman
    SKU:28065 - 500 µg

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  • 10(E)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. It inhibits IFN-γ-induced production of kynurenine in THP-1 cells by 14% when used at a concentration of 20 µM.{40333} 10(E)-Pentadecenoic acid has been used in studies of alternative β-oxidation pathways.{35136,35135}  

     

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    Cayman
    SKU:22467 -

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  • 10(E)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. It inhibits IFN-γ-induced production of kynurenine in THP-1 cells by 14% when used at a concentration of 20 µM.{40333} 10(E)-Pentadecenoic acid has been used in studies of alternative β-oxidation pathways.{35136,35135}  

     

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    Cayman
    SKU:22467 -

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  • 10(E)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. It inhibits IFN-γ-induced production of kynurenine in THP-1 cells by 14% when used at a concentration of 20 µM.{40333} 10(E)-Pentadecenoic acid has been used in studies of alternative β-oxidation pathways.{35136,35135}  

     

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    Cayman
    SKU:22467 -

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  • 10(E)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. It inhibits IFN-γ-induced production of kynurenine in THP-1 cells by 14% when used at a concentration of 20 µM.{40333} 10(E)-Pentadecenoic acid has been used in studies of alternative β-oxidation pathways.{35136,35135}  

     

    Brand:
    Cayman
    SKU:22467 -

    Out of stock

  • Conjugated linoleic acid (CLA) refers to a family of 8 geometric isomers of linoleic acid in which the two double bonds are contiguous. (The predominant form of linoleic acid in nature, 18:ω6, has double bonds at 9 and 12, interrupted by a methylene carbon.) CLA is found in both meat and dairy products, but it is not found to any significant degree in plants. The predominant isomer of CLA in animal tissue is 9Z,11E; smaller amounts of 10E,12Z also occur. Various antioxidant and antitumor activities have been attributed to CLA or its downstream metabolites.{6849} Reported health benefits of dietary supplementation with CLA have been attributed variously to competitive inhibition of Δ6-desaturase and/or PPARγ activation.{6980} [Matreya, LLC. Catalog No. 1249]  

     

    Brand:
    Cayman
    SKU:90145 - 10 mg

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  • Conjugated linoleic acid (CLA) refers to a family of 8 geometric isomers of linoleic acid in which the two double bonds are contiguous. (The predominant form of linoleic acid in nature, 18:ω6, has double bonds at 9 and 12, interrupted by a methylene carbon.) CLA is found in both meat and dairy products, but it is not found to any significant degree in plants. The predominant isomer of CLA in animal tissue is 9Z,11E; smaller amounts of 10E,12Z also occur. Various antioxidant and antitumor activities have been attributed to CLA or its downstream metabolites.{6849} Reported health benefits of dietary supplementation with CLA have been attributed variously to competitive inhibition of Δ6-desaturase and/or PPARγ activation.{6980} [Matreya, LLC. Catalog No. 1249]  

     

    Brand:
    Cayman
    SKU:90145 - 25 mg

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  • Conjugated linoleic acid (CLA) refers to a family of 8 geometric isomers of linoleic acid in which the two double bonds are contiguous. (The predominant form of linoleic acid in nature, 18:ω6, has double bonds at 9 and 12, interrupted by a methylene carbon.) CLA is found in both meat and dairy products, but it is not found to any significant degree in plants. The predominant isomer of CLA in animal tissue is 9Z,11E; smaller amounts of 10E,12Z also occur. Various antioxidant and antitumor activities have been attributed to CLA or its downstream metabolites.{6849} Reported health benefits of dietary supplementation with CLA have been attributed variously to competitive inhibition of Δ6-desaturase and/or PPARγ activation.{6980} [Matreya, LLC. Catalog No. 1249]  

     

    Brand:
    Cayman
    SKU:90145 - 5 mg

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  • Conjugated linoleic acid (CLA) refers to a family of 8 geometric isomers of linoleic acid in which the two double bonds are contiguous. (The predominant form of linoleic acid in nature, 18:ω6, has double bonds at 9 and 12, interrupted by a methylene carbon.) CLA is found in both meat and dairy products, but it is not found to any significant degree in plants. The predominant isomer of CLA in animal tissue is 9Z,11E; smaller amounts of 10E,12Z also occur. Various antioxidant and antitumor activities have been attributed to CLA or its downstream metabolites.{6849} Reported health benefits of dietary supplementation with CLA have been attributed variously to competitive inhibition of Δ6-desaturase and/or PPARγ activation.{6980} [Matreya, LLC. Catalog No. 1249]  

     

    Brand:
    Cayman
    SKU:90145 - 50 mg

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  • 10(E),12(Z)-Conjugated linoleic acid methyl ester has been used as a standard in the quantification of 10(E),12(Z)-conjugated linoleic acid from L. plantarum culture samples.{39659} [Matreya, LLC. Catalog No. 1254]  

     

    Brand:
    Cayman
    SKU:24584 - 25 mg

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  • Protectin D1 (also known as neuroprotectin D1 when produced in neuronal tissues) is a DHA-derived dihydroxy fatty acid that exhibits potent protective and anti-inflammatory activities.{14974,14973,14972} 10(S),17(S)-DiHDHA is a DHA metabolite, also referred to as protectin DX (PDX).{19393} It is produced by an apparent double lipoxygenase (LO)-mediated reaction in murine peritonitis exudates, in suspensions of human leukocytes, or by soybean 15-LO incubated with DHA.{14974,19393} It differs from protectin D1 with respect to the stereochemistry of the C-10 hydroxyl and the double bond configuration at the 13 and 15 positions. 10(S),17(S)-DiHDHA blocks neutrophil infiltration in murine peritonitis by 20-25% at a dose of 1 ng/mouse.{14974} It also inhibits platelet activation by both impairing thromboxane (TX) synthesis and TX receptor activation.{19393,19394}  

     

    Brand:
    Cayman
    SKU:10008128 - 100 µg

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  • Protectin D1 (also known as neuroprotectin D1 when produced in neuronal tissues) is a DHA-derived dihydroxy fatty acid that exhibits potent protective and anti-inflammatory activities.{14974,14973,14972} 10(S),17(S)-DiHDHA is a DHA metabolite, also referred to as protectin DX (PDX).{19393} It is produced by an apparent double lipoxygenase (LO)-mediated reaction in murine peritonitis exudates, in suspensions of human leukocytes, or by soybean 15-LO incubated with DHA.{14974,19393} It differs from protectin D1 with respect to the stereochemistry of the C-10 hydroxyl and the double bond configuration at the 13 and 15 positions. 10(S),17(S)-DiHDHA blocks neutrophil infiltration in murine peritonitis by 20-25% at a dose of 1 ng/mouse.{14974} It also inhibits platelet activation by both impairing thromboxane (TX) synthesis and TX receptor activation.{19393,19394}  

     

    Brand:
    Cayman
    SKU:10008128 - 25 µg

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  • Protectin D1 (also known as neuroprotectin D1 when produced in neuronal tissues) is a DHA-derived dihydroxy fatty acid that exhibits potent protective and anti-inflammatory activities.{14974,14973,14972} 10(S),17(S)-DiHDHA is a DHA metabolite, also referred to as protectin DX (PDX).{19393} It is produced by an apparent double lipoxygenase (LO)-mediated reaction in murine peritonitis exudates, in suspensions of human leukocytes, or by soybean 15-LO incubated with DHA.{14974,19393} It differs from protectin D1 with respect to the stereochemistry of the C-10 hydroxyl and the double bond configuration at the 13 and 15 positions. 10(S),17(S)-DiHDHA blocks neutrophil infiltration in murine peritonitis by 20-25% at a dose of 1 ng/mouse.{14974} It also inhibits platelet activation by both impairing thromboxane (TX) synthesis and TX receptor activation.{19393,19394}  

     

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    Cayman
    SKU:10008128 - 50 µg

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  • 10(Z)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. 10(Z)-Pentadecenoic acid inhibits IFN-γ-induced production of kynurenine in Thp-1 cells by 16%.{40333}  

     

    Brand:
    Cayman
    SKU:22362 -

    Out of stock

  • 10(Z)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. 10(Z)-Pentadecenoic acid inhibits IFN-γ-induced production of kynurenine in Thp-1 cells by 16%.{40333}  

     

    Brand:
    Cayman
    SKU:22362 -

    Out of stock

  • 10(Z)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. 10(Z)-Pentadecenoic acid inhibits IFN-γ-induced production of kynurenine in Thp-1 cells by 16%.{40333}  

     

    Brand:
    Cayman
    SKU:22362 -

    Out of stock

  • 10(Z)-Pentadecenoic acid is a 15-carbon, long-chain monounsaturated fatty acid. 10(Z)-Pentadecenoic acid inhibits IFN-γ-induced production of kynurenine in Thp-1 cells by 16%.{40333}  

     

    Brand:
    Cayman
    SKU:22362 -

    Out of stock

  • 10(Z)-Pentadecenoic acid methyl ester is a methyl ester form of the fatty acid 10(Z)-pentadecenoic acid (Item No. 22362). It has been used as a standard for the quantification of pentadecenoic acid in vernix caseosa.{36627} [Matreya, LLC. Catalog No. 1210]  

     

    Brand:
    Cayman
    SKU:26729 - 50 mg

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  • The Myc proto-oncogenes interact with Max to form a dimer that regulates gene transcription. The protein c-Myc, in particular, promotes gene expression relevant to cell growth and thus drives cancer. 10058-F4 is a cell-permeable thiazolidinone that inhibits the dimerization of c-Myc and Max at 64 µM, preventing c-Myc-dependent gene expression and cell proliferation.{25765} It induces cell cycle arrest, apoptosis, and myeloid differentiation at 100 µM in human acute myeloid leukemia cells.{25762} 10058-F4 is rapidly metabolized in mice when given intravenously, limiting its effects on tumors in vivo.{25761} In addition to c-Myc, 10058-F4 inhibits the nuclear Myc protein, N-Myc, at 50 µM, inducing arrest, apoptosis, and differentiation in neuroblastoma cells overexpressing the gene for N-Myc.{25763} This compound can be used to delineate novel actions of Myc proteins, especially those related to lipid and glucose metabolism.{25763,25764}  

     

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    SKU:-
  • The Myc proto-oncogenes interact with Max to form a dimer that regulates gene transcription. The protein c-Myc, in particular, promotes gene expression relevant to cell growth and thus drives cancer. 10058-F4 is a cell-permeable thiazolidinone that inhibits the dimerization of c-Myc and Max at 64 µM, preventing c-Myc-dependent gene expression and cell proliferation.{25765} It induces cell cycle arrest, apoptosis, and myeloid differentiation at 100 µM in human acute myeloid leukemia cells.{25762} 10058-F4 is rapidly metabolized in mice when given intravenously, limiting its effects on tumors in vivo.{25761} In addition to c-Myc, 10058-F4 inhibits the nuclear Myc protein, N-Myc, at 50 µM, inducing arrest, apoptosis, and differentiation in neuroblastoma cells overexpressing the gene for N-Myc.{25763} This compound can be used to delineate novel actions of Myc proteins, especially those related to lipid and glucose metabolism.{25763,25764}  

     

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    Cayman
    SKU:-
  • The Myc proto-oncogenes interact with Max to form a dimer that regulates gene transcription. The protein c-Myc, in particular, promotes gene expression relevant to cell growth and thus drives cancer. 10058-F4 is a cell-permeable thiazolidinone that inhibits the dimerization of c-Myc and Max at 64 µM, preventing c-Myc-dependent gene expression and cell proliferation.{25765} It induces cell cycle arrest, apoptosis, and myeloid differentiation at 100 µM in human acute myeloid leukemia cells.{25762} 10058-F4 is rapidly metabolized in mice when given intravenously, limiting its effects on tumors in vivo.{25761} In addition to c-Myc, 10058-F4 inhibits the nuclear Myc protein, N-Myc, at 50 µM, inducing arrest, apoptosis, and differentiation in neuroblastoma cells overexpressing the gene for N-Myc.{25763} This compound can be used to delineate novel actions of Myc proteins, especially those related to lipid and glucose metabolism.{25763,25764}  

     

    Brand:
    Cayman
    SKU:-
  • The Myc proto-oncogenes interact with Max to form a dimer that regulates gene transcription. The protein c-Myc, in particular, promotes gene expression relevant to cell growth and thus drives cancer. 10058-F4 is a cell-permeable thiazolidinone that inhibits the dimerization of c-Myc and Max at 64 µM, preventing c-Myc-dependent gene expression and cell proliferation.{25765} It induces cell cycle arrest, apoptosis, and myeloid differentiation at 100 µM in human acute myeloid leukemia cells.{25762} 10058-F4 is rapidly metabolized in mice when given intravenously, limiting its effects on tumors in vivo.{25761} In addition to c-Myc, 10058-F4 inhibits the nuclear Myc protein, N-Myc, at 50 µM, inducing arrest, apoptosis, and differentiation in neuroblastoma cells overexpressing the gene for N-Myc.{25763} This compound can be used to delineate novel actions of Myc proteins, especially those related to lipid and glucose metabolism.{25763,25764}  

     

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    Cayman
    SKU:-
  • The c-Myc oncoprotein is overexpressed in many tumors and is essential for maintaining the proliferation of transformed cells. To function as a transcription factor, c-Myc must dimerize with Max via the basic helix-loop-helix leucine zipper protein (bHLH-ZIP) domains in each protein. 10074-G5 is a c-Myc inhibitor that binds to and distorts the bHLH-ZIP domain of c-Myc (Kd = 2.8 µM), thereby inhibiting c-Myc/Max heterodimer formation and inhibiting its transcriptional activity (IC50 = 146 µM).{30637,30638,30640} 10074-G5 is cytotoxic to c-Myc-overexpressing cells lines with IC50 values of 15.6 and 13.5 µM for Daudi Burkitt lymphoma cells and HL60 promyelocytic leukemia cells, respectively.{30636} 10074-G5 can also interfere with N-Myc/Max interactions (Kd = 19.2 µM for binding the bHLH-Zip of N-Myc), inducing apoptosis in N-Myc amplified neuroblastoma Kelly cells (IC50 = 22.5 µM).{30639}  

     

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    SKU:-

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  • The c-Myc oncoprotein is overexpressed in many tumors and is essential for maintaining the proliferation of transformed cells. To function as a transcription factor, c-Myc must dimerize with Max via the basic helix-loop-helix leucine zipper protein (bHLH-ZIP) domains in each protein. 10074-G5 is a c-Myc inhibitor that binds to and distorts the bHLH-ZIP domain of c-Myc (Kd = 2.8 µM), thereby inhibiting c-Myc/Max heterodimer formation and inhibiting its transcriptional activity (IC50 = 146 µM).{30637,30638,30640} 10074-G5 is cytotoxic to c-Myc-overexpressing cells lines with IC50 values of 15.6 and 13.5 µM for Daudi Burkitt lymphoma cells and HL60 promyelocytic leukemia cells, respectively.{30636} 10074-G5 can also interfere with N-Myc/Max interactions (Kd = 19.2 µM for binding the bHLH-Zip of N-Myc), inducing apoptosis in N-Myc amplified neuroblastoma Kelly cells (IC50 = 22.5 µM).{30639}  

     

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    Cayman
    SKU:-

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  • The c-Myc oncoprotein is overexpressed in many tumors and is essential for maintaining the proliferation of transformed cells. To function as a transcription factor, c-Myc must dimerize with Max via the basic helix-loop-helix leucine zipper protein (bHLH-ZIP) domains in each protein. 10074-G5 is a c-Myc inhibitor that binds to and distorts the bHLH-ZIP domain of c-Myc (Kd = 2.8 µM), thereby inhibiting c-Myc/Max heterodimer formation and inhibiting its transcriptional activity (IC50 = 146 µM).{30637,30638,30640} 10074-G5 is cytotoxic to c-Myc-overexpressing cells lines with IC50 values of 15.6 and 13.5 µM for Daudi Burkitt lymphoma cells and HL60 promyelocytic leukemia cells, respectively.{30636} 10074-G5 can also interfere with N-Myc/Max interactions (Kd = 19.2 µM for binding the bHLH-Zip of N-Myc), inducing apoptosis in N-Myc amplified neuroblastoma Kelly cells (IC50 = 22.5 µM).{30639}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • The c-Myc oncoprotein is overexpressed in many tumors and is essential for maintaining the proliferation of transformed cells. To function as a transcription factor, c-Myc must dimerize with Max via the basic helix-loop-helix leucine zipper protein (bHLH-ZIP) domains in each protein. 10074-G5 is a c-Myc inhibitor that binds to and distorts the bHLH-ZIP domain of c-Myc (Kd = 2.8 µM), thereby inhibiting c-Myc/Max heterodimer formation and inhibiting its transcriptional activity (IC50 = 146 µM).{30637,30638,30640} 10074-G5 is cytotoxic to c-Myc-overexpressing cells lines with IC50 values of 15.6 and 13.5 µM for Daudi Burkitt lymphoma cells and HL60 promyelocytic leukemia cells, respectively.{30636} 10074-G5 can also interfere with N-Myc/Max interactions (Kd = 19.2 µM for binding the bHLH-Zip of N-Myc), inducing apoptosis in N-Myc amplified neuroblastoma Kelly cells (IC50 = 22.5 µM).{30639}  

     

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    Cayman
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  • 10Z-Hymenialdisine is a natural marine sponge alkaloid with numerous cellular actions. Most notably, it blocks signaling through the Raf-1/MEK-1/MAPK pathway by potently inhibiting MEK-1 (IC50 = 9 nM).{24027} Hymenialdisine also inhibits numerous kinases in vitro, most notably GSK3β, CDK1/cyclin B, CDK5/p25, CK1, and CDK2/cyclin E (IC50s = 10, 22, 28, 35, and 40 nM, respectively), as well as, less potently, ERK1/2 and several isoforms of PKC.{28027,24024} Early studies demonstrated that it suppresses inflammatory gene expression by blocking signaling through NF-κB at micromolar concentrations.{28028} At similar concentrations, hymenialdisine also blocks bacterial quorum sensing.{28029}  

     

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  • 11-cis Retinal is a chromophore that binds to opsin in the mammalian visual system as an inverse agonist forming the inactive conformation of rhodopsin.{29223} When 11-cis retinal absorbs a photon of light, it isomerizes to form all-trans retinal (Item No. 18449) beginning the phototransduction cycle, which is the basis for mammalian vision. A G121L mutation in opsin allows 11-cis retinal to bind as a partial agonist and activate rhodopsin in the absence of light.{38067} In a moth model of carotenoid deficiency-induced low visual sensitivity, 11-cis retinal application to compound eyes restored visual sensitivity almost completely.{38066}  

     

    Brand:
    Cayman
    SKU:21377 -

    Out of stock

  • 11-cis Retinal is a chromophore that binds to opsin in the mammalian visual system as an inverse agonist forming the inactive conformation of rhodopsin.{29223} When 11-cis retinal absorbs a photon of light, it isomerizes to form all-trans retinal (Item No. 18449) beginning the phototransduction cycle, which is the basis for mammalian vision. A G121L mutation in opsin allows 11-cis retinal to bind as a partial agonist and activate rhodopsin in the absence of light.{38067} In a moth model of carotenoid deficiency-induced low visual sensitivity, 11-cis retinal application to compound eyes restored visual sensitivity almost completely.{38066}  

     

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    Cayman
    SKU:21377 -

    Out of stock

  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile hydrocarbon pheromones. 11-cis Vaccenyl acetate is the male-specific mating pheromone of the fruit fly D. melanogaster. It acts selectively through the Or67d odorant receptor to control mating behavior in both male and female fruit flies.{14950}  

     

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    Cayman
    SKU:10010101 - 10 mg

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  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile hydrocarbon pheromones. 11-cis Vaccenyl acetate is the male-specific mating pheromone of the fruit fly D. melanogaster. It acts selectively through the Or67d odorant receptor to control mating behavior in both male and female fruit flies.{14950}  

     

    Brand:
    Cayman
    SKU:10010101 - 100 mg

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  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile hydrocarbon pheromones. 11-cis Vaccenyl acetate is the male-specific mating pheromone of the fruit fly D. melanogaster. It acts selectively through the Or67d odorant receptor to control mating behavior in both male and female fruit flies.{14950}  

     

    Brand:
    Cayman
    SKU:10010101 - 5 mg

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  • The mating and social behaviors of insects are largely orchestrated by a suite of volatile hydrocarbon pheromones. 11-cis Vaccenyl acetate is the male-specific mating pheromone of the fruit fly D. melanogaster. It acts selectively through the Or67d odorant receptor to control mating behavior in both male and female fruit flies.{14950}  

     

    Brand:
    Cayman
    SKU:10010101 - 50 mg

    Available on backorder

  • Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518} Urinary concentrations of 11-dehydro TXB2 are approximately 30-70 ng/mmol creatinine.{6109,7635}  

     

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    Cayman
    SKU:-

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  • Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518} Urinary concentrations of 11-dehydro TXB2 are approximately 30-70 ng/mmol creatinine.{6109,7635}  

     

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    Cayman
    SKU:-

    Available on backorder

  • Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518} Urinary concentrations of 11-dehydro TXB2 are approximately 30-70 ng/mmol creatinine.{6109,7635}  

     

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    Cayman
    SKU:-

    Available on backorder

  • Thromboxane B2 (TXB2) is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518} Urinary concentrations of 11-dehydro TXB2 are approximately 30-70 ng/mmol creatinine.{6109,7635}  

     

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    Cayman
    SKU:-

    Available on backorder

  • Thromboxane A2 (TXA2), produced from arachidonic acid, causes irreversible platelet aggregation, vascular, and bronchial smooth muscle contraction. TXA2 is rapidly hydrolyzed non-enzymatically to form TXB2. However, most of the TXB2 measured in the plasma or urine of healthy individuals is due to ex vivo platelet activation or intra-renal production, and normal concentrations of circulating TXB2 are extremely low (1-2 pg/ml) and highly transient (t½ = 5-7 minutes). 11-dehydro TXB2 is a metabolite of TXB2 (not formed by platelets or the kidney) with a circulating half-life (t½) of 45 minutes. Its measurement in plasma or urine will give a time-integrated indication of TXA2 production and is recommended to estimate TXA2 levels to circumvent measurement complications associated with TXB2. Cayman’s 11-dehydro TXB2 ELISA Kit is a competitive assay that can be used for quantification of 11-dehydro TXB2 in urine and other sample matrices. Normal plasma levels of 11-dehydro TXB2 (1-2 pg/ml) are below the detection limit of this assay (16 pg/ml), so plasma samples must be purified and concentrated prior to analysis. Urine samples should be diluted appropriately before assaying. There is evidence suggesting that 11-dehydro TXB2 can be formed non-enzymatically following platelet activation, so it is important to process plasma samples quickly to prevent artifactual formation of 11-dehydro TXB2. The assay has a range from 15.6-2,000 pg/ml and a sensitivity (80% B/B0) of approximately 34 pg/ml.  

     

    Brand:
    Cayman
    SKU:519510 - 480 solid wells

    Available on backorder

  • Thromboxane A2 (TXA2), produced from arachidonic acid, causes irreversible platelet aggregation, vascular, and bronchial smooth muscle contraction. TXA2 is rapidly hydrolyzed non-enzymatically to form TXB2. However, most of the TXB2 measured in the plasma or urine of healthy individuals is due to ex vivo platelet activation or intra-renal production, and normal concentrations of circulating TXB2 are extremely low (1-2 pg/ml) and highly transient (t½ = 5-7 minutes). 11-dehydro TXB2 is a metabolite of TXB2 (not formed by platelets or the kidney) with a circulating half-life (t½) of 45 minutes. Its measurement in plasma or urine will give a time-integrated indication of TXA2 production and is recommended to estimate TXA2 levels to circumvent measurement complications associated with TXB2. Cayman’s 11-dehydro TXB2 ELISA Kit is a competitive assay that can be used for quantification of 11-dehydro TXB2 in urine and other sample matrices. Normal plasma levels of 11-dehydro TXB2 (1-2 pg/ml) are below the detection limit of this assay (16 pg/ml), so plasma samples must be purified and concentrated prior to analysis. Urine samples should be diluted appropriately before assaying. There is evidence suggesting that 11-dehydro TXB2 can be formed non-enzymatically following platelet activation, so it is important to process plasma samples quickly to prevent artifactual formation of 11-dehydro TXB2. The assay has a range from 15.6-2,000 pg/ml and a sensitivity (80% B/B0) of approximately 34 pg/ml.  

     

    Brand:
    Cayman
    SKU:519510 - 480 strip wells

    Available on backorder

  • Thromboxane A2 (TXA2), produced from arachidonic acid, causes irreversible platelet aggregation, vascular, and bronchial smooth muscle contraction. TXA2 is rapidly hydrolyzed non-enzymatically to form TXB2. However, most of the TXB2 measured in the plasma or urine of healthy individuals is due to ex vivo platelet activation or intra-renal production, and normal concentrations of circulating TXB2 are extremely low (1-2 pg/ml) and highly transient (t½ = 5-7 minutes). 11-dehydro TXB2 is a metabolite of TXB2 (not formed by platelets or the kidney) with a circulating half-life (t½) of 45 minutes. Its measurement in plasma or urine will give a time-integrated indication of TXA2 production and is recommended to estimate TXA2 levels to circumvent measurement complications associated with TXB2. Cayman’s 11-dehydro TXB2 ELISA Kit is a competitive assay that can be used for quantification of 11-dehydro TXB2 in urine and other sample matrices. Normal plasma levels of 11-dehydro TXB2 (1-2 pg/ml) are below the detection limit of this assay (16 pg/ml), so plasma samples must be purified and concentrated prior to analysis. Urine samples should be diluted appropriately before assaying. There is evidence suggesting that 11-dehydro TXB2 can be formed non-enzymatically following platelet activation, so it is important to process plasma samples quickly to prevent artifactual formation of 11-dehydro TXB2. The assay has a range from 15.6-2,000 pg/ml and a sensitivity (80% B/B0) of approximately 34 pg/ml.  

     

    Brand:
    Cayman
    SKU:519510 - 96 solid wells

    Available on backorder

  • Thromboxane A2 (TXA2), produced from arachidonic acid, causes irreversible platelet aggregation, vascular, and bronchial smooth muscle contraction. TXA2 is rapidly hydrolyzed non-enzymatically to form TXB2. However, most of the TXB2 measured in the plasma or urine of healthy individuals is due to ex vivo platelet activation or intra-renal production, and normal concentrations of circulating TXB2 are extremely low (1-2 pg/ml) and highly transient (t½ = 5-7 minutes). 11-dehydro TXB2 is a metabolite of TXB2 (not formed by platelets or the kidney) with a circulating half-life (t½) of 45 minutes. Its measurement in plasma or urine will give a time-integrated indication of TXA2 production and is recommended to estimate TXA2 levels to circumvent measurement complications associated with TXB2. Cayman’s 11-dehydro TXB2 ELISA Kit is a competitive assay that can be used for quantification of 11-dehydro TXB2 in urine and other sample matrices. Normal plasma levels of 11-dehydro TXB2 (1-2 pg/ml) are below the detection limit of this assay (16 pg/ml), so plasma samples must be purified and concentrated prior to analysis. Urine samples should be diluted appropriately before assaying. There is evidence suggesting that 11-dehydro TXB2 can be formed non-enzymatically following platelet activation, so it is important to process plasma samples quickly to prevent artifactual formation of 11-dehydro TXB2. The assay has a range from 15.6-2,000 pg/ml and a sensitivity (80% B/B0) of approximately 34 pg/ml.  

     

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    Cayman
    SKU:519510 - 96 strip wells

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  • Brand:
    Cayman
    SKU:419512 - 100 dtn

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  • Brand:
    Cayman
    SKU:419512- 100 dtn

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    SKU:419512 - 500 dtn

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  • Brand:
    Cayman
    SKU:419512- 500 dtn

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  • 11-dehydro Thromboxane B2 Monoclonal Assay Buffer Concentrate (10X) has been formulated and tested to work with Cayman’s ELISA Kits. Detailed instructions for its use are contained in the respective Cayman ELISA Kit booklet.  

     

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    Cayman
    SKU:419517 - 10 ml

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  • Brand:
    Cayman
    SKU:419514 - 100 ng

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  • 11-dehydro Thromboxane B2-d4 (TXB2-d4) is intended for use as an internal standard for the quantification of 11-dehydro TXB2 (Item No. 19500) by stable isotope dilution MS. TXB2 is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518}  

     

    Brand:
    Cayman
    SKU:319500 - 100 µg

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  • 11-dehydro Thromboxane B2-d4 (TXB2-d4) is intended for use as an internal standard for the quantification of 11-dehydro TXB2 (Item No. 19500) by stable isotope dilution MS. TXB2 is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518}  

     

    Brand:
    Cayman
    SKU:319500 - 25 µg

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  • 11-dehydro Thromboxane B2-d4 (TXB2-d4) is intended for use as an internal standard for the quantification of 11-dehydro TXB2 (Item No. 19500) by stable isotope dilution MS. TXB2 is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518}  

     

    Brand:
    Cayman
    SKU:319500 - 50 µg

    Available on backorder

  • 11-dehydro Thromboxane B2-d4 (TXB2-d4) is intended for use as an internal standard for the quantification of 11-dehydro TXB2 (Item No. 19500) by stable isotope dilution MS. TXB2 is released in substantial quantities from aggregating platelets and metabolized during circulation to 11-dehydro TXB2 and 2,3-dinor TXB2.{1410} 11-dehydro TXB2 is one of the main plasma metabolites of TXB2 and can be used as a marker for in vivo TXA2 synthesis.{1410,438,278,518} The mean plasma level in human males is 0.9-4.3 pg/ml and the half life is 45-60 minutes.{438,278,518}  

     

    Brand:
    Cayman
    SKU:319500 - 500 µg

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  • 11-dehydro TXB3 is a urinary metabolite of TXA3 in humans with enhanced dietary intake of EPA.{1923}  

     

    Brand:
    Cayman
    SKU:19995 -

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  • 11-dehydro TXB3 is a urinary metabolite of TXA3 in humans with enhanced dietary intake of EPA.{1923}  

     

    Brand:
    Cayman
    SKU:19995 -

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  • 11-dehydro TXB3 is a urinary metabolite of TXA3 in humans with enhanced dietary intake of EPA.{1923}  

     

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    Cayman
    SKU:19995 -

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  • 11-dehydro-2,3-dinor Thromboxane B2 (11-dehydro-2,3-dinor TXB2) has been identified as a TXB2 (Item No. 19030) metabolite in human urine by GC/MS.{264} The relative abundance is only about one-tenth that of 11-dehydro TXB2(Item No. 19500), making it unlikely that 11-dehydro-2,3-dinor TXB2 will be used widely as an index of thromboxane synthesis.{1249,2018}  

     

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    Cayman
    SKU:-

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  • 11-dehydro-2,3-dinor Thromboxane B2 (11-dehydro-2,3-dinor TXB2) has been identified as a TXB2 (Item No. 19030) metabolite in human urine by GC/MS.{264} The relative abundance is only about one-tenth that of 11-dehydro TXB2(Item No. 19500), making it unlikely that 11-dehydro-2,3-dinor TXB2 will be used widely as an index of thromboxane synthesis.{1249,2018}  

     

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    Cayman
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  • 11-dehydro-2,3-dinor Thromboxane B2 (11-dehydro-2,3-dinor TXB2) has been identified as a TXB2 (Item No. 19030) metabolite in human urine by GC/MS.{264} The relative abundance is only about one-tenth that of 11-dehydro TXB2(Item No. 19500), making it unlikely that 11-dehydro-2,3-dinor TXB2 will be used widely as an index of thromboxane synthesis.{1249,2018}  

     

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    Cayman
    SKU:-

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  • 11-dehydro-2,3-dinor Thromboxane B2 (11-dehydro-2,3-dinor TXB2) has been identified as a TXB2 (Item No. 19030) metabolite in human urine by GC/MS.{264} The relative abundance is only about one-tenth that of 11-dehydro TXB2(Item No. 19500), making it unlikely that 11-dehydro-2,3-dinor TXB2 will be used widely as an index of thromboxane synthesis.{1249,2018}  

     

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  • 11-deoxy Corticosterone (DOC) is an endogenous mineralocorticoid synthesized in the zona fasciculata and zona glomerulosa of the adrenal gland.{41026} It is a metabolite of progesterone (Item No. 15876) and precursor to aldosterone (Item No. 15273) and corticosterone (Item No. 16063).{41025} DOC is metabolized to the neuroactive compound (3α,5α)-2,21-dihydroxypregnan-20-one (THDOC), which positively modulates GABAA receptors and produces effects similar to barbiturates in rats.{41027} Injections of naloxone (Item Nos. 15594 | ISO60191) and corticotropin-releasing hormone (CRH) increase, while dexamethasone decreases, DOC in cynomolgus monkeys.{41026} DOC levels are increased 3.4-fold in obese and diabetic mice.{41025}  

     

    Brand:
    Cayman
    SKU:22916 - 100 mg

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  • 11-deoxy Corticosterone (DOC) is an endogenous mineralocorticoid synthesized in the zona fasciculata and zona glomerulosa of the adrenal gland.{41026} It is a metabolite of progesterone (Item No. 15876) and precursor to aldosterone (Item No. 15273) and corticosterone (Item No. 16063).{41025} DOC is metabolized to the neuroactive compound (3α,5α)-2,21-dihydroxypregnan-20-one (THDOC), which positively modulates GABAA receptors and produces effects similar to barbiturates in rats.{41027} Injections of naloxone (Item Nos. 15594 | ISO60191) and corticotropin-releasing hormone (CRH) increase, while dexamethasone decreases, DOC in cynomolgus monkeys.{41026} DOC levels are increased 3.4-fold in obese and diabetic mice.{41025}  

     

    Brand:
    Cayman
    SKU:22916 - 25 mg

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  • 11-deoxy Corticosterone (DOC) is an endogenous mineralocorticoid synthesized in the zona fasciculata and zona glomerulosa of the adrenal gland.{41026} It is a metabolite of progesterone (Item No. 15876) and precursor to aldosterone (Item No. 15273) and corticosterone (Item No. 16063).{41025} DOC is metabolized to the neuroactive compound (3α,5α)-2,21-dihydroxypregnan-20-one (THDOC), which positively modulates GABAA receptors and produces effects similar to barbiturates in rats.{41027} Injections of naloxone (Item Nos. 15594 | ISO60191) and corticotropin-releasing hormone (CRH) increase, while dexamethasone decreases, DOC in cynomolgus monkeys.{41026} DOC levels are increased 3.4-fold in obese and diabetic mice.{41025}  

     

    Brand:
    Cayman
    SKU:22916 - 50 mg

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  • 11-deoxy Prostaglandin E1 (11-deoxy PGE1) is a synthetic analog of PGE1. Early reports show that it is a selective agonist for the EP2 receptor but effective at much higher concentrations than PGE2.{1360,1026} However, later studies show that it is a non-selective agonist of EP receptors and stimulates cAMP release in Jurkat cells with an EC50 of 0.25 µM.{2120} 11-deoxy PGE1 also exhibits vasodepressor and bronchodilator responses in guinea pigs.{2217} 11-deoxy PGE1 exhibits selectively for the mouse EP3 receptor and is essentially equipotent to PGE1 at this receptor subtype. The Ki values for binding to the mouse EP1, EP2, EP3, and EP4 receptors are 600, 45, 1.1, and 23 nM, respectively.{6640}  

     

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    Cayman
    SKU:-
  • 11-deoxy Prostaglandin E1 (11-deoxy PGE1) is a synthetic analog of PGE1. Early reports show that it is a selective agonist for the EP2 receptor but effective at much higher concentrations than PGE2.{1360,1026} However, later studies show that it is a non-selective agonist of EP receptors and stimulates cAMP release in Jurkat cells with an EC50 of 0.25 µM.{2120} 11-deoxy PGE1 also exhibits vasodepressor and bronchodilator responses in guinea pigs.{2217} 11-deoxy PGE1 exhibits selectively for the mouse EP3 receptor and is essentially equipotent to PGE1 at this receptor subtype. The Ki values for binding to the mouse EP1, EP2, EP3, and EP4 receptors are 600, 45, 1.1, and 23 nM, respectively.{6640}  

     

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    Cayman
    SKU:-
  • 11-deoxy Prostaglandin E1 (11-deoxy PGE1) is a synthetic analog of PGE1. Early reports show that it is a selective agonist for the EP2 receptor but effective at much higher concentrations than PGE2.{1360,1026} However, later studies show that it is a non-selective agonist of EP receptors and stimulates cAMP release in Jurkat cells with an EC50 of 0.25 µM.{2120} 11-deoxy PGE1 also exhibits vasodepressor and bronchodilator responses in guinea pigs.{2217} 11-deoxy PGE1 exhibits selectively for the mouse EP3 receptor and is essentially equipotent to PGE1 at this receptor subtype. The Ki values for binding to the mouse EP1, EP2, EP3, and EP4 receptors are 600, 45, 1.1, and 23 nM, respectively.{6640}  

     

    Brand:
    Cayman
    SKU:-
  • 11-deoxy Prostaglandin E1 (11-deoxy PGE1) is a synthetic analog of PGE1. Early reports show that it is a selective agonist for the EP2 receptor but effective at much higher concentrations than PGE2.{1360,1026} However, later studies show that it is a non-selective agonist of EP receptors and stimulates cAMP release in Jurkat cells with an EC50 of 0.25 µM.{2120} 11-deoxy PGE1 also exhibits vasodepressor and bronchodilator responses in guinea pigs.{2217} 11-deoxy PGE1 exhibits selectively for the mouse EP3 receptor and is essentially equipotent to PGE1 at this receptor subtype. The Ki values for binding to the mouse EP1, EP2, EP3, and EP4 receptors are 600, 45, 1.1, and 23 nM, respectively.{6640}  

     

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    Cayman
    SKU:-
  • 11-deoxy Prostaglandin E2 (11-deoxy PGE2) is a stable, synthetic analog of PGE2 (Item No. 14010). In contrast to PGE2 which has bronchodilation effects, 11-deoxy PGE2 is a powerful bronchoconstrictor and contracts human respiratory tract smooth muscle with potencies ranging from 5 to 30 times higher than PGF2α (Item No. 16010).{2218}  

     

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    Cayman
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  • 11-deoxy Prostaglandin E2 (11-deoxy PGE2) is a stable, synthetic analog of PGE2 (Item No. 14010). In contrast to PGE2 which has bronchodilation effects, 11-deoxy PGE2 is a powerful bronchoconstrictor and contracts human respiratory tract smooth muscle with potencies ranging from 5 to 30 times higher than PGF2α (Item No. 16010).{2218}  

     

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    Cayman
    SKU:-
  • 11-deoxy Prostaglandin E2 (11-deoxy PGE2) is a stable, synthetic analog of PGE2 (Item No. 14010). In contrast to PGE2 which has bronchodilation effects, 11-deoxy PGE2 is a powerful bronchoconstrictor and contracts human respiratory tract smooth muscle with potencies ranging from 5 to 30 times higher than PGF2α (Item No. 16010).{2218}  

     

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    Cayman
    SKU:-
  • 11-deoxy PGF1α is a synthetic analog of PGF1α. In whole animal studies, a dose of 32 mg/kg inhibited gastric acid secretion by 35%.{1347} 11-deoxy PGF1α is also known to cause rat uterine contractions at a dose 0.3 times that of PGF1α.{1348} It also exhibits vasopressor and bronchoconstrictor activities at about half the potency of PGF2α in guinea pigs.{2217}  

     

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    Cayman
    SKU:-
  • 11-deoxy PGF1α is a synthetic analog of PGF1α. In whole animal studies, a dose of 32 mg/kg inhibited gastric acid secretion by 35%.{1347} 11-deoxy PGF1α is also known to cause rat uterine contractions at a dose 0.3 times that of PGF1α.{1348} It also exhibits vasopressor and bronchoconstrictor activities at about half the potency of PGF2α in guinea pigs.{2217}  

     

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    Cayman
    SKU:-
  • 11-deoxy PGF1α is a synthetic analog of PGF1α. In whole animal studies, a dose of 32 mg/kg inhibited gastric acid secretion by 35%.{1347} 11-deoxy PGF1α is also known to cause rat uterine contractions at a dose 0.3 times that of PGF1α.{1348} It also exhibits vasopressor and bronchoconstrictor activities at about half the potency of PGF2α in guinea pigs.{2217}  

     

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    Cayman
    SKU:-
  • 11-deoxy PGF1β is a synthetic analog of PGF1β. In contrast to PGF2α and PGF1α, 11-deoxy PGF1β exhibits vasodepressor and bronchodilator activities in guinea pigs at a dose of 500 µg/kg.{2217}  

     

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    Cayman
    SKU:-
  • 11-deoxy PGF1β is a synthetic analog of PGF1β. In contrast to PGF2α and PGF1α, 11-deoxy PGF1β exhibits vasodepressor and bronchodilator activities in guinea pigs at a dose of 500 µg/kg.{2217}  

     

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    Cayman
    SKU:-
  • 11-deoxy PGF1β is a synthetic analog of PGF1β. In contrast to PGF2α and PGF1α, 11-deoxy PGF1β exhibits vasodepressor and bronchodilator activities in guinea pigs at a dose of 500 µg/kg.{2217}  

     

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    Cayman
    SKU:-
  • 11-deoxy PGF2α is a synthetic analog of PGF2α. It is a more potent agonist than PGF2α at inducing smooth muscle contractions of rabbit aorta, dog saphenous vein, and guinea pig trachea.{2260} It is approximately 20% less potent than U-46619.{2260}  

     

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    Cayman
    SKU:-

    Out of stock

  • 11-deoxy PGF2α is a synthetic analog of PGF2α. It is a more potent agonist than PGF2α at inducing smooth muscle contractions of rabbit aorta, dog saphenous vein, and guinea pig trachea.{2260} It is approximately 20% less potent than U-46619.{2260}  

     

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    Cayman
    SKU:-

    Out of stock

  • 11-deoxy PGF2α is a synthetic analog of PGF2α. It is a more potent agonist than PGF2α at inducing smooth muscle contractions of rabbit aorta, dog saphenous vein, and guinea pig trachea.{2260} It is approximately 20% less potent than U-46619.{2260}  

     

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    Cayman
    SKU:-

    Out of stock

  • 11-deoxy Prostaglandin F2β (11-deoxy PGF2β) is an analog of PGF2β (Item No. 16410). There are no published reports on the biological activity of 11-deoxy PGF2β.  

     

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    Cayman
    SKU:-

    Out of stock

  • 11-deoxy Prostaglandin F2β (11-deoxy PGF2β) is an analog of PGF2β (Item No. 16410). There are no published reports on the biological activity of 11-deoxy PGF2β.  

     

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    Cayman
    SKU:-

    Out of stock

  • 11-deoxy Prostaglandin F2β (11-deoxy PGF2β) is an analog of PGF2β (Item No. 16410). There are no published reports on the biological activity of 11-deoxy PGF2β.  

     

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    Cayman
    SKU:-

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  • Prostaglandin D2 (PGD2; Item No. 12010) is one of the five primary enzymatic prostaglandins derived directly from PGH2 (Item No. 17020). PGD2 is produced abundantly in the CSF by the lipocalin-type PGD synthase, and in the periphery by myeloid cells including mast cells and basophils by a second, leukocyte-type PGD synthase.{9588} PGD2 is chemically unstable, and its use and analysis is complicated by its short in vivo half-life. 11-deoxy-11-methylene PGD2 is a novel, chemically stable, isosteric analog of PGD2 wherein the 11-keto group is replaced by an exocyclic methylene. In the PGE series, the analogous modification leads to a stable, somewhat less potent agonist which embodies the same uterine stimulant and cervical ripening activities as the parent prostaglandin.{7894} However, 11-deoxy-11-methylene PGD2 has been reported by one group to be essentially without agonist activity on human platelets, a DP1 receptor assay.{11175} The CRTH2-receptor actions of 11-deoxy-11-methylene PGD2 are not yet reported.  

     

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    Cayman
    SKU:12410 - 1 mg

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  • Prostaglandin D2 (PGD2; Item No. 12010) is one of the five primary enzymatic prostaglandins derived directly from PGH2 (Item No. 17020). PGD2 is produced abundantly in the CSF by the lipocalin-type PGD synthase, and in the periphery by myeloid cells including mast cells and basophils by a second, leukocyte-type PGD synthase.{9588} PGD2 is chemically unstable, and its use and analysis is complicated by its short in vivo half-life. 11-deoxy-11-methylene PGD2 is a novel, chemically stable, isosteric analog of PGD2 wherein the 11-keto group is replaced by an exocyclic methylene. In the PGE series, the analogous modification leads to a stable, somewhat less potent agonist which embodies the same uterine stimulant and cervical ripening activities as the parent prostaglandin.{7894} However, 11-deoxy-11-methylene PGD2 has been reported by one group to be essentially without agonist activity on human platelets, a DP1 receptor assay.{11175} The CRTH2-receptor actions of 11-deoxy-11-methylene PGD2 are not yet reported.  

     

    Brand:
    Cayman
    SKU:12410 - 10 mg

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  • Prostaglandin D2 (PGD2; Item No. 12010) is one of the five primary enzymatic prostaglandins derived directly from PGH2 (Item No. 17020). PGD2 is produced abundantly in the CSF by the lipocalin-type PGD synthase, and in the periphery by myeloid cells including mast cells and basophils by a second, leukocyte-type PGD synthase.{9588} PGD2 is chemically unstable, and its use and analysis is complicated by its short in vivo half-life. 11-deoxy-11-methylene PGD2 is a novel, chemically stable, isosteric analog of PGD2 wherein the 11-keto group is replaced by an exocyclic methylene. In the PGE series, the analogous modification leads to a stable, somewhat less potent agonist which embodies the same uterine stimulant and cervical ripening activities as the parent prostaglandin.{7894} However, 11-deoxy-11-methylene PGD2 has been reported by one group to be essentially without agonist activity on human platelets, a DP1 receptor assay.{11175} The CRTH2-receptor actions of 11-deoxy-11-methylene PGD2 are not yet reported.  

     

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    Cayman
    SKU:12410 - 5 mg

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  • 11-deoxy-16,16-dimethyl PGE2 is a stable synthetic analog of PGE2. It is an agonist for both EP2 and EP3 receptors.{3620} It is an effective inhibitor of gastric acid secretion and ulcer formation in the rat, with ED50 values of 1 mg/kg and 0.021 mg/kg respectively.{1147} It is 900 times more potent than PGF2α in the contraction of human respiratory tract smooth muscle in vitro.{2218}  

     

    Brand:
    Cayman
    SKU:-
  • 11-deoxy-16,16-dimethyl PGE2 is a stable synthetic analog of PGE2. It is an agonist for both EP2 and EP3 receptors.{3620} It is an effective inhibitor of gastric acid secretion and ulcer formation in the rat, with ED50 values of 1 mg/kg and 0.021 mg/kg respectively.{1147} It is 900 times more potent than PGF2α in the contraction of human respiratory tract smooth muscle in vitro.{2218}  

     

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    Cayman
    SKU:-
  • 11-deoxy-16,16-dimethyl PGE2 is a stable synthetic analog of PGE2. It is an agonist for both EP2 and EP3 receptors.{3620} It is an effective inhibitor of gastric acid secretion and ulcer formation in the rat, with ED50 values of 1 mg/kg and 0.021 mg/kg respectively.{1147} It is 900 times more potent than PGF2α in the contraction of human respiratory tract smooth muscle in vitro.{2218}  

     

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  • 11-Hexadecenoic acid is a monounsaturated fatty acid. 11-cis-Hexadecenoic acid and 11-trans-hexadecenoic acid have been found in ewe milk fat, and levels of each increase with dietary lipid supplementation of linseed, sunflower, olive, or fish oils.{47172} 11-trans-Hexadecenoic acid has also been found in intramuscular fat samples isolated from male and female foals.{47173} This product is a mixture of 11-cis- and 11-trans-hexadecenoic acids. [Matreya, LLC. Catalog No. 1208]  

     

    Brand:
    Cayman
    SKU:26730 - 10 mg

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  • 11-Hexadecenoic acid is a monounsaturated fatty acid. 11-cis-Hexadecenoic acid and 11-trans-hexadecenoic acid have been found in ewe milk fat, and levels of each increase with dietary lipid supplementation of linseed, sunflower, olive, or fish oils.{47172} 11-trans-Hexadecenoic acid has also been found in intramuscular fat samples isolated from male and female foals.{47173} This product is a mixture of 11-cis- and 11-trans-hexadecenoic acids. [Matreya, LLC. Catalog No. 1208]  

     

    Brand:
    Cayman
    SKU:26730 - 25 mg

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  • 11-Hexadecenoic acid is a monounsaturated fatty acid. 11-cis-Hexadecenoic acid and 11-trans-hexadecenoic acid have been found in ewe milk fat, and levels of each increase with dietary lipid supplementation of linseed, sunflower, olive, or fish oils.{47172} 11-trans-Hexadecenoic acid has also been found in intramuscular fat samples isolated from male and female foals.{47173} This product is a mixture of 11-cis- and 11-trans-hexadecenoic acids. [Matreya, LLC. Catalog No. 1208]  

     

    Brand:
    Cayman
    SKU:26730 - 5 mg

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  • 11-Hexadecenoic acid is a monounsaturated fatty acid. 11-cis-Hexadecenoic acid and 11-trans-hexadecenoic acid have been found in ewe milk fat, and levels of each increase with dietary lipid supplementation of linseed, sunflower, olive, or fish oils.{47172} 11-trans-Hexadecenoic acid has also been found in intramuscular fat samples isolated from male and female foals.{47173} This product is a mixture of 11-cis- and 11-trans-hexadecenoic acids. [Matreya, LLC. Catalog No. 1208]  

     

    Brand:
    Cayman
    SKU:26730 - 50 mg

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  • 11-keto Fluprostenol is an analog of prostaglandin D2 (PGD2) with structural modifications intended to give it a prolonged half-life and greater potency. Fluprostenol is a well-studied, potent analog of PGF2α and acts primarily through the FP receptor.{1182} Oxidation at C-11 of fluprostenol yields 11-keto fluprostenol. 11-keto Fluprostenol exhibits moderate binding to the CRTH2/DP2 receptor compared to PGD2 and essentially no activity at the DP1 receptor.{10723}  

     

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    Cayman
    SKU:-

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  • 11-keto Fluprostenol is an analog of prostaglandin D2 (PGD2) with structural modifications intended to give it a prolonged half-life and greater potency. Fluprostenol is a well-studied, potent analog of PGF2α and acts primarily through the FP receptor.{1182} Oxidation at C-11 of fluprostenol yields 11-keto fluprostenol. 11-keto Fluprostenol exhibits moderate binding to the CRTH2/DP2 receptor compared to PGD2 and essentially no activity at the DP1 receptor.{10723}  

     

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    Cayman
    SKU:-

    Out of stock

  • 11-keto Fluprostenol is an analog of prostaglandin D2 (PGD2) with structural modifications intended to give it a prolonged half-life and greater potency. Fluprostenol is a well-studied, potent analog of PGF2α and acts primarily through the FP receptor.{1182} Oxidation at C-11 of fluprostenol yields 11-keto fluprostenol. 11-keto Fluprostenol exhibits moderate binding to the CRTH2/DP2 receptor compared to PGD2 and essentially no activity at the DP1 receptor.{10723}  

     

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    Cayman
    SKU:-

    Out of stock

  • Brand:
    Cayman
    SKU:482752 - 100 dtn

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  • Brand:
    Cayman
    SKU:482752 - 500 dtn

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  • While testosterone is the primary androgenic male steroid found in mammals, 11-keto testosterone (11-KT) is a second key androgenic steroid found in fish. It occurs in males together with testosterone in amounts which vary from less than 1 ng/ml to as much as 50-100 ng/ml, depending on the species and the stage of the reproductive cycle. In the sea bass, testosterone concentrations are generally higher than 11-KT, with peak levels found after the spawning season. 11-KT, on the other hand, remains at levels less than 1 ng/ml but rises abruptly to 4-6 ng/ml during spermiation at the height of the spawning season.{8544} 11-KT also shows individual variations in Arctic char, with dominant males having significantly higher 11-KT levels.{8325}  

     

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    Cayman
    SKU:582751 - 480 solid wells

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  • While testosterone is the primary androgenic male steroid found in mammals, 11-keto testosterone (11-KT) is a second key androgenic steroid found in fish. It occurs in males together with testosterone in amounts which vary from less than 1 ng/ml to as much as 50-100 ng/ml, depending on the species and the stage of the reproductive cycle. In the sea bass, testosterone concentrations are generally higher than 11-KT, with peak levels found after the spawning season. 11-KT, on the other hand, remains at levels less than 1 ng/ml but rises abruptly to 4-6 ng/ml during spermiation at the height of the spawning season.{8544} 11-KT also shows individual variations in Arctic char, with dominant males having significantly higher 11-KT levels.{8325}  

     

    Brand:
    Cayman
    SKU:582751 - 480 strip wells

    Available on backorder

  • While testosterone is the primary androgenic male steroid found in mammals, 11-keto testosterone (11-KT) is a second key androgenic steroid found in fish. It occurs in males together with testosterone in amounts which vary from less than 1 ng/ml to as much as 50-100 ng/ml, depending on the species and the stage of the reproductive cycle. In the sea bass, testosterone concentrations are generally higher than 11-KT, with peak levels found after the spawning season. 11-KT, on the other hand, remains at levels less than 1 ng/ml but rises abruptly to 4-6 ng/ml during spermiation at the height of the spawning season.{8544} 11-KT also shows individual variations in Arctic char, with dominant males having significantly higher 11-KT levels.{8325}  

     

    Brand:
    Cayman
    SKU:582751 - 96 solid wells

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  • While testosterone is the primary androgenic male steroid found in mammals, 11-keto testosterone (11-KT) is a second key androgenic steroid found in fish. It occurs in males together with testosterone in amounts which vary from less than 1 ng/ml to as much as 50-100 ng/ml, depending on the species and the stage of the reproductive cycle. In the sea bass, testosterone concentrations are generally higher than 11-KT, with peak levels found after the spawning season. 11-KT, on the other hand, remains at levels less than 1 ng/ml but rises abruptly to 4-6 ng/ml during spermiation at the height of the spawning season.{8544} 11-KT also shows individual variations in Arctic char, with dominant males having significantly higher 11-KT levels.{8325}  

     

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    Cayman
    SKU:582751 - 96 strip wells

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  • Brand:
    Cayman
    SKU:482754 - 1 ea

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  • 11-keto-β-Boswellic acid is a naturally occurring pentacyclic triterpene isolated from the gum resin exudate from the stem of the tree B. serrata (frankincense).{30044} Boswellic acids are specific, non-redox inhibitors of leukotriene synthesis via 5-lipoxygenase that demonstrate anti-inflammatory and anti-arthritic actions.{6066,30045,30046}  

     

    Brand:
    Cayman
    SKU:11668 - 1 mg

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  • 11-keto-β-Boswellic acid is a naturally occurring pentacyclic triterpene isolated from the gum resin exudate from the stem of the tree B. serrata (frankincense).{30044} Boswellic acids are specific, non-redox inhibitors of leukotriene synthesis via 5-lipoxygenase that demonstrate anti-inflammatory and anti-arthritic actions.{6066,30045,30046}  

     

    Brand:
    Cayman
    SKU:11668 - 10 mg

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  • 11-keto-β-Boswellic acid is a naturally occurring pentacyclic triterpene isolated from the gum resin exudate from the stem of the tree B. serrata (frankincense).{30044} Boswellic acids are specific, non-redox inhibitors of leukotriene synthesis via 5-lipoxygenase that demonstrate anti-inflammatory and anti-arthritic actions.{6066,30045,30046}  

     

    Brand:
    Cayman
    SKU:11668 - 5 mg

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  • 11-methyl Lauric acid methyl ester is a methylated fatty acid methyl ester that has been used as a standard in the quantification of 11-methyl lauric acid in vernix caseosa and M. oleifera extract.{36627,36628} [Matreya, LLC. Catalog No. 1656]  

     

    Brand:
    Cayman
    SKU:24809 - 1 mg

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  • 11-methyl Lauric acid methyl ester is a methylated fatty acid methyl ester that has been used as a standard in the quantification of 11-methyl lauric acid in vernix caseosa and M. oleifera extract.{36627,36628} [Matreya, LLC. Catalog No. 1656]  

     

    Brand:
    Cayman
    SKU:24809 - 5 mg

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  • 11-O-Methylpseurotin A is a fungal metabolite originally isolated from A. fumigatus.{48248} It decreases survival of hof1Δ mutant strains of S. cerevisiae.  

     

    Brand:
    Cayman
    SKU:27734 - 1 mg

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  • 11-O-Methylpseurotin A is a fungal metabolite originally isolated from A. fumigatus.{48248} It decreases survival of hof1Δ mutant strains of S. cerevisiae.  

     

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    Cayman
    SKU:27734 - 5 mg

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  • 11-O-Methylpseurotin A is a fungal metabolite originally isolated from A. fumigatus.{48248} It decreases survival of hof1Δ mutant strains of S. cerevisiae.  

     

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    Cayman
    SKU:27734 - 500 µg

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  • 11-oxo Mogroside V is a sweet tasting cucurbitane glycoside derivative of mogroside V (Item No. 19853). It has antioxidant effects against both O2- and OH- (EC50s = 4.79 and 16.52 µg/ml, respectively) and prevents OH-induced DNA damage (EC50 = 3.09 µg/ml).{34666} 11-oxo Mogroside V also inhibits carcinogenesis in murine models.{34667}  

     

    Brand:
    Cayman
    SKU:22416 -

    Out of stock

  • 11-oxo Mogroside V is a sweet tasting cucurbitane glycoside derivative of mogroside V (Item No. 19853). It has antioxidant effects against both O2- and OH- (EC50s = 4.79 and 16.52 µg/ml, respectively) and prevents OH-induced DNA damage (EC50 = 3.09 µg/ml).{34666} 11-oxo Mogroside V also inhibits carcinogenesis in murine models.{34667}  

     

    Brand:
    Cayman
    SKU:22416 -

    Out of stock

  • 11-oxo Mogroside V is a sweet tasting cucurbitane glycoside derivative of mogroside V (Item No. 19853). It has antioxidant effects against both O2- and OH- (EC50s = 4.79 and 16.52 µg/ml, respectively) and prevents OH-induced DNA damage (EC50 = 3.09 µg/ml).{34666} 11-oxo Mogroside V also inhibits carcinogenesis in murine models.{34667}  

     

    Brand:
    Cayman
    SKU:22416 -

    Out of stock

  • 11-oxo Mogroside V is a sweet tasting cucurbitane glycoside derivative of mogroside V (Item No. 19853). It has antioxidant effects against both O2- and OH- (EC50s = 4.79 and 16.52 µg/ml, respectively) and prevents OH-induced DNA damage (EC50 = 3.09 µg/ml).{34666} 11-oxo Mogroside V also inhibits carcinogenesis in murine models.{34667}  

     

    Brand:
    Cayman
    SKU:22416 -

    Out of stock

  • 11-Oxoetiocholanolone is a metabolite of cortisol that is found in the feces of ungulates and other animals. Stress-induced glucocorticoids (cortisol, corticosterone) traditionally have been measured through blood sampling, but the collection process is known to cause stress in animals, interfering with experimental results.{19086} Fecal sample analysis provides more accurate detection of stress hormones, and it can be used to measure stress in both laboratory and free-ranging animals.{19086} 11-Oxoetiocholanolone is also found in human urine. Increased levels of urinary 11-oxoetiocholanolone have been observed in the latter part of pregnancy and in patients with uterine leiomyomas.{35076,35077} A study of postmenopausal women determined that 11-oxoetiocholanolone was indicative of stress-induced urinary incontinence.{35075}  

     

    Brand:
    Cayman
    SKU:501420 - 96 solid wells

    Available on backorder

  • 11-Oxoetiocholanolone is a metabolite of cortisol that is found in the feces of ungulates and other animals. Stress-induced glucocorticoids (cortisol, corticosterone) traditionally have been measured through blood sampling, but the collection process is known to cause stress in animals, interfering with experimental results.{19086} Fecal sample analysis provides more accurate detection of stress hormones, and it can be used to measure stress in both laboratory and free-ranging animals.{19086} 11-Oxoetiocholanolone is also found in human urine. Increased levels of urinary 11-oxoetiocholanolone have been observed in the latter part of pregnancy and in patients with uterine leiomyomas.{35076,35077} A study of postmenopausal women determined that 11-oxoetiocholanolone was indicative of stress-induced urinary incontinence.{35075}  

     

    Brand:
    Cayman
    SKU:501420 - 96 strip wells

    Available on backorder