Chemicals

Showing 14551–14700 of 41137 results

  • Cholesteryl hemisuccinate is a cholesterol ester with anticancer activity.{36854} It inhibits the growth of murine C1498 myeloid and L1210 lymphocytic leukemia cells when used at concentrations of 50 and 150 μM, respectively.{36854} Cholesteryl hemisuccinate acts as an ionizable anionic detergent and is commonly used to stabilize unilamellar vesicles and liposomes.{36855} It has also been used as an emulsifying agent in various vesicular drug delivery systems for anticancer drugs, antibiotics, and oligonucleotides and to solubilize various proteins including chemokine receptor 1 as well as erythrocyte ghosts.{24443,36856,36857}  

     

    Brand:
    Cayman
    SKU:25698 - 1 g

    Available on backorder

  • Cholesteryl hemisuccinate is a cholesterol ester with anticancer activity.{36854} It inhibits the growth of murine C1498 myeloid and L1210 lymphocytic leukemia cells when used at concentrations of 50 and 150 μM, respectively.{36854} Cholesteryl hemisuccinate acts as an ionizable anionic detergent and is commonly used to stabilize unilamellar vesicles and liposomes.{36855} It has also been used as an emulsifying agent in various vesicular drug delivery systems for anticancer drugs, antibiotics, and oligonucleotides and to solubilize various proteins including chemokine receptor 1 as well as erythrocyte ghosts.{24443,36856,36857}  

     

    Brand:
    Cayman
    SKU:25698 - 10 g

    Available on backorder

  • Cholesteryl hemisuccinate is a cholesterol ester with anticancer activity.{36854} It inhibits the growth of murine C1498 myeloid and L1210 lymphocytic leukemia cells when used at concentrations of 50 and 150 μM, respectively.{36854} Cholesteryl hemisuccinate acts as an ionizable anionic detergent and is commonly used to stabilize unilamellar vesicles and liposomes.{36855} It has also been used as an emulsifying agent in various vesicular drug delivery systems for anticancer drugs, antibiotics, and oligonucleotides and to solubilize various proteins including chemokine receptor 1 as well as erythrocyte ghosts.{24443,36856,36857}  

     

    Brand:
    Cayman
    SKU:25698 - 25 g

    Available on backorder

  • Cholesteryl hemisuccinate is a cholesterol ester with anticancer activity.{36854} It inhibits the growth of murine C1498 myeloid and L1210 lymphocytic leukemia cells when used at concentrations of 50 and 150 μM, respectively.{36854} Cholesteryl hemisuccinate acts as an ionizable anionic detergent and is commonly used to stabilize unilamellar vesicles and liposomes.{36855} It has also been used as an emulsifying agent in various vesicular drug delivery systems for anticancer drugs, antibiotics, and oligonucleotides and to solubilize various proteins including chemokine receptor 1 as well as erythrocyte ghosts.{24443,36856,36857}  

     

    Brand:
    Cayman
    SKU:25698 - 5 g

    Available on backorder

  • Cholesteryl heptadecanoate is a cholesterol ester (CE) formed by the condensation of cholesterol with heptadecanoic acid, a C-17 saturated fatty acid that does not occur in any natural animal or vegetable fat at high concentrations.{34595} As such, it is commonly used as an internal standard for the quantification of cholesterol esters by GC- or LC-mass spectrometry. CEs are major constituents of lipoprotein particles carried in blood and accumulate in the fatty acid lesions of atherosclerotic plaques.{34591,34594} CEs of various fatty acids are major constituents of murine and human adrenal glands.{34592}  

     

    Brand:
    Cayman
    SKU:21750 -

    Out of stock

  • Cholesteryl heptadecanoate is a cholesterol ester (CE) formed by the condensation of cholesterol with heptadecanoic acid, a C-17 saturated fatty acid that does not occur in any natural animal or vegetable fat at high concentrations.{34595} As such, it is commonly used as an internal standard for the quantification of cholesterol esters by GC- or LC-mass spectrometry. CEs are major constituents of lipoprotein particles carried in blood and accumulate in the fatty acid lesions of atherosclerotic plaques.{34591,34594} CEs of various fatty acids are major constituents of murine and human adrenal glands.{34592}  

     

    Brand:
    Cayman
    SKU:21750 -

    Out of stock

  • Cholesteryl heptadecanoate is a cholesterol ester (CE) formed by the condensation of cholesterol with heptadecanoic acid, a C-17 saturated fatty acid that does not occur in any natural animal or vegetable fat at high concentrations.{34595} As such, it is commonly used as an internal standard for the quantification of cholesterol esters by GC- or LC-mass spectrometry. CEs are major constituents of lipoprotein particles carried in blood and accumulate in the fatty acid lesions of atherosclerotic plaques.{34591,34594} CEs of various fatty acids are major constituents of murine and human adrenal glands.{34592}  

     

    Brand:
    Cayman
    SKU:21750 -

    Out of stock

  • Cholesteryl heptadecanoate is a cholesterol ester (CE) formed by the condensation of cholesterol with heptadecanoic acid, a C-17 saturated fatty acid that does not occur in any natural animal or vegetable fat at high concentrations.{34595} As such, it is commonly used as an internal standard for the quantification of cholesterol esters by GC- or LC-mass spectrometry. CEs are major constituents of lipoprotein particles carried in blood and accumulate in the fatty acid lesions of atherosclerotic plaques.{34591,34594} CEs of various fatty acids are major constituents of murine and human adrenal glands.{34592}  

     

    Brand:
    Cayman
    SKU:21750 -

    Out of stock

  • Cholesteryl homo-γ-linolenate is a cholesterol ester. It accumulates in the adrenal gland of rabbits fed a diet high in linolenic acid.{49041} Levels of cholesteryl homo-γ-linolenate are decreased and positively correlate with cognitive decline in HIV-infected humans.{49042}  

     

    Brand:
    Cayman
    SKU:26469 - 1 mg

    Available on backorder

  • Cholesteryl homo-γ-linolenate is a cholesterol ester. It accumulates in the adrenal gland of rabbits fed a diet high in linolenic acid.{49041} Levels of cholesteryl homo-γ-linolenate are decreased and positively correlate with cognitive decline in HIV-infected humans.{49042}  

     

    Brand:
    Cayman
    SKU:26469 - 10 mg

    Available on backorder

  • Cholesteryl homo-γ-linolenate is a cholesterol ester. It accumulates in the adrenal gland of rabbits fed a diet high in linolenic acid.{49041} Levels of cholesteryl homo-γ-linolenate are decreased and positively correlate with cognitive decline in HIV-infected humans.{49042}  

     

    Brand:
    Cayman
    SKU:26469 - 25 mg

    Available on backorder

  • Cholesteryl homo-γ-linolenate is a cholesterol ester. It accumulates in the adrenal gland of rabbits fed a diet high in linolenic acid.{49041} Levels of cholesteryl homo-γ-linolenate are decreased and positively correlate with cognitive decline in HIV-infected humans.{49042}  

     

    Brand:
    Cayman
    SKU:26469 - 5 mg

    Available on backorder

  • Cholesteryl lignocerate is a cholesterol ester that has been found in human meibum.{47142} Cholesteryl lignocerate can be hydrolyzed by cellular extracts from cultured human skin fibroblasts isolated from healthy individuals but not patients with cholesteryl ester storage disease (CESD) or Wolman disease.{48151}  

     

    Brand:
    Cayman
    SKU:26470 - 10 mg

    Available on backorder

  • Cholesteryl lignocerate is a cholesterol ester that has been found in human meibum.{47142} Cholesteryl lignocerate can be hydrolyzed by cellular extracts from cultured human skin fibroblasts isolated from healthy individuals but not patients with cholesteryl ester storage disease (CESD) or Wolman disease.{48151}  

     

    Brand:
    Cayman
    SKU:26470 - 25 mg

    Available on backorder

  • Cholesteryl lignocerate is a cholesterol ester that has been found in human meibum.{47142} Cholesteryl lignocerate can be hydrolyzed by cellular extracts from cultured human skin fibroblasts isolated from healthy individuals but not patients with cholesteryl ester storage disease (CESD) or Wolman disease.{48151}  

     

    Brand:
    Cayman
    SKU:26470 - 5 mg

    Available on backorder

  • Cholesteryl lignocerate is a cholesterol ester that has been found in human meibum.{47142} Cholesteryl lignocerate can be hydrolyzed by cellular extracts from cultured human skin fibroblasts isolated from healthy individuals but not patients with cholesteryl ester storage disease (CESD) or Wolman disease.{48151}  

     

    Brand:
    Cayman
    SKU:26470 - 50 mg

    Available on backorder

  • Cholesteryl linoleate is a cholesterol ester found in LDL.{38440} Cholesteryl linoleate is transferred to the plasma membrane of macrophages and CHO cells expressing 15-lipoxygenase (15-LO) via LDL receptor-related protein (LRP), where it undergoes oxidation to form cholesteryl linoleate hydroperoxides (Item No. 48001). Cholesteryl linoleate expression increases 2.7-fold in Apob-lipoproteins in mice overexpressing the human ABCA1 reverse cholesterol transporter, directly correlating with increased levels of hepatic cholesterol and number of atherosclerotic lesions.{38441}  

     

    Brand:
    Cayman
    SKU:22597 -

    Out of stock

  • Cholesteryl linoleate is a cholesterol ester found in LDL.{38440} Cholesteryl linoleate is transferred to the plasma membrane of macrophages and CHO cells expressing 15-lipoxygenase (15-LO) via LDL receptor-related protein (LRP), where it undergoes oxidation to form cholesteryl linoleate hydroperoxides (Item No. 48001). Cholesteryl linoleate expression increases 2.7-fold in Apob-lipoproteins in mice overexpressing the human ABCA1 reverse cholesterol transporter, directly correlating with increased levels of hepatic cholesterol and number of atherosclerotic lesions.{38441}  

     

    Brand:
    Cayman
    SKU:22597 -

    Out of stock

  • Cholesteryl linoleate is a cholesterol ester found in LDL.{38440} Cholesteryl linoleate is transferred to the plasma membrane of macrophages and CHO cells expressing 15-lipoxygenase (15-LO) via LDL receptor-related protein (LRP), where it undergoes oxidation to form cholesteryl linoleate hydroperoxides (Item No. 48001). Cholesteryl linoleate expression increases 2.7-fold in Apob-lipoproteins in mice overexpressing the human ABCA1 reverse cholesterol transporter, directly correlating with increased levels of hepatic cholesterol and number of atherosclerotic lesions.{38441}  

     

    Brand:
    Cayman
    SKU:22597 -

    Out of stock

  • Cholesteryl linoleate is a cholesterol ester found in LDL.{38440} Cholesteryl linoleate is transferred to the plasma membrane of macrophages and CHO cells expressing 15-lipoxygenase (15-LO) via LDL receptor-related protein (LRP), where it undergoes oxidation to form cholesteryl linoleate hydroperoxides (Item No. 48001). Cholesteryl linoleate expression increases 2.7-fold in Apob-lipoproteins in mice overexpressing the human ABCA1 reverse cholesterol transporter, directly correlating with increased levels of hepatic cholesterol and number of atherosclerotic lesions.{38441}  

     

    Brand:
    Cayman
    SKU:22597 -

    Out of stock

  • Cholesteryl myristate is a cholesterol ester.{49007} Levels of cholesteryl myristate are increased in the serum, liver, and aorta in rabbits fed a high-cholesterol diet and positively correlate with development of non-alcoholic fatty liver disease (NAFLD). Plasma levels of cholesteryl myristate also positively correlate with the presence of unstable atherosclerotic plaques in coronary artery disease.{49008} Cholesterol myristate has been used in the composition of lipid nanoparticles as drug carrier systems for drugs with low water solubility.{36419}  

     

    Brand:
    Cayman
    SKU:26439 - 1 g

    Available on backorder

  • Cholesteryl myristate is a cholesterol ester.{49007} Levels of cholesteryl myristate are increased in the serum, liver, and aorta in rabbits fed a high-cholesterol diet and positively correlate with development of non-alcoholic fatty liver disease (NAFLD). Plasma levels of cholesteryl myristate also positively correlate with the presence of unstable atherosclerotic plaques in coronary artery disease.{49008} Cholesterol myristate has been used in the composition of lipid nanoparticles as drug carrier systems for drugs with low water solubility.{36419}  

     

    Brand:
    Cayman
    SKU:26439 - 500 mg

    Available on backorder

  • Cholesteryl oleate is a cholesterol ester.{43911,45131} It has been used in the generation of nanoparticles and liposomes for drug delivery.  

     

    Brand:
    Cayman
    SKU:26472 - 100 mg

    Available on backorder

  • Cholesteryl oleate is a cholesterol ester.{43911,45131} It has been used in the generation of nanoparticles and liposomes for drug delivery.  

     

    Brand:
    Cayman
    SKU:26472 - 250 mg

    Available on backorder

  • Cholesteryl oleate is a cholesterol ester.{43911,45131} It has been used in the generation of nanoparticles and liposomes for drug delivery.  

     

    Brand:
    Cayman
    SKU:26472 - 50 mg

    Available on backorder

  • Cholesteryl oleate is a cholesterol ester.{43911,45131} It has been used in the generation of nanoparticles and liposomes for drug delivery.  

     

    Brand:
    Cayman
    SKU:26472 - 500 mg

    Available on backorder

  • Cholesteryl palmitate is a cholesterol ester. It is a major cholesterol ester found in human meibum and has been used to form a stable tear film to study amphiphilic block copolymers as surfactants for dry eyes.{45234} Cholesteryl palmitate levels in amniotic fluid are decreased in pregnancies in which infants later developed respiratory distress syndrome and in patients with well-controlled diabetes.{45235,45236} Levels of cholesteryl palmitate are increased in bronchoalveolar lavage fluid (BALF) from patients with chronic interstitial pneumonia.{45237}  

     

    Brand:
    Cayman
    SKU:26473 - 1 g

    Available on backorder

  • Cholesteryl palmitate is a cholesterol ester. It is a major cholesterol ester found in human meibum and has been used to form a stable tear film to study amphiphilic block copolymers as surfactants for dry eyes.{45234} Cholesteryl palmitate levels in amniotic fluid are decreased in pregnancies in which infants later developed respiratory distress syndrome and in patients with well-controlled diabetes.{45235,45236} Levels of cholesteryl palmitate are increased in bronchoalveolar lavage fluid (BALF) from patients with chronic interstitial pneumonia.{45237} Cholesteryl palmitate MaxSpec® standard is a quantitative grade standard of cholesteryl palmitate (Item No. 26473) that has been prepared specifically for mass spectrometry and related applications where quantitative reproducibility is required. The solution has been prepared gravimetrically and is supplied in a deactivated glass ampule sealed under argon. The concentration was verified by comparison to an independently prepared calibration standard. This cholesteryl palmitate MaxSpec® standard is guaranteed to meet identity, purity, stability, and concentration specifications and is provided with a batch-specific certificate of analysis. Ongoing stability testing is performed to ensure the concentration remains accurate throughout the shelf life of the product. Note: The amount of solution added to the vial is in excess of the listed amount. Therefore, it is necessary to accurately measure volumes for preparation of calibration standards. Follow recommended storage and handling conditions to maintain product quality.  

     

    Brand:
    Cayman
    SKU:30250 - 100 µg

    Available on backorder

  • Cholesteryl palmitoleate is a cholesterol ester.{42811,47069,42812} Plasma levels of cholesteryl palmitoleate are increased in ApoE-/- mice exposed to cigarette smoke and in pediatric patients with biliary atresia.{42811,47069} Cholesteryl palmitoleate has been used as a standard for the identification of cholesterol esters in human meibomian gland secretions.{42812}  

     

    Brand:
    Cayman
    SKU:26474 - 100 mg

    Available on backorder

  • Cholesteryl palmitoleate is a cholesterol ester.{42811,47069,42812} Plasma levels of cholesteryl palmitoleate are increased in ApoE-/- mice exposed to cigarette smoke and in pediatric patients with biliary atresia.{42811,47069} Cholesteryl palmitoleate has been used as a standard for the identification of cholesterol esters in human meibomian gland secretions.{42812}  

     

    Brand:
    Cayman
    SKU:26474 - 250 mg

    Available on backorder

  • Cholesteryl palmitoleate is a cholesterol ester.{42811,47069,42812} Plasma levels of cholesteryl palmitoleate are increased in ApoE-/- mice exposed to cigarette smoke and in pediatric patients with biliary atresia.{42811,47069} Cholesteryl palmitoleate has been used as a standard for the identification of cholesterol esters in human meibomian gland secretions.{42812}  

     

    Brand:
    Cayman
    SKU:26474 - 50 mg

    Available on backorder

  • Cholesteryl palmitoleate is a cholesterol ester.{42811,47069,42812} Plasma levels of cholesteryl palmitoleate are increased in ApoE-/- mice exposed to cigarette smoke and in pediatric patients with biliary atresia.{42811,47069} Cholesteryl palmitoleate has been used as a standard for the identification of cholesterol esters in human meibomian gland secretions.{42812}  

     

    Brand:
    Cayman
    SKU:26474 - 500 mg

    Available on backorder

  • Cholesteryl stearate is a cholesterol ester.{47414} It has been used as an internal standard for the quantification of sterol esters in various plant tissues by quadropole time-of-flight (Q-TOF) MS. Cholesteryl stearate levels are decreased in coronary arteries with atherosclerotic plaques, isolated fatty streaks, and isolated atherosclerotic plaques compared with non-atherosclerotic coronary arteries.{47415}  

     

    Brand:
    Cayman
    SKU:26475 - 250 mg

    Available on backorder

  • Cholesteryl stearate is a cholesterol ester.{47414} It has been used as an internal standard for the quantification of sterol esters in various plant tissues by quadropole time-of-flight (Q-TOF) MS. Cholesteryl stearate levels are decreased in coronary arteries with atherosclerotic plaques, isolated fatty streaks, and isolated atherosclerotic plaques compared with non-atherosclerotic coronary arteries.{47415}  

     

    Brand:
    Cayman
    SKU:26475 - 500 mg

    Available on backorder

  • Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716}  

     

    Brand:
    Cayman
    SKU:20250 -

    Available on backorder

  • Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716}  

     

    Brand:
    Cayman
    SKU:20250 -

    Available on backorder

  • Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716}  

     

    Brand:
    Cayman
    SKU:20250 -

    Available on backorder

  • Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716}  

     

    Brand:
    Cayman
    SKU:20250 -

    Available on backorder

  • Cholic acid 7-sulfate is a metabolite of the primary bile acid cholic acid (Item No. 20250).{30822,30823} It is produced by conjugation of a sulfate group with the hydroxy group at position 7 of cholic acid in the liver and gut. Fecal levels of cholic acid 7-sulfate are increased in male, but not female, mice fed a diet supplemented with cholic acid or chenodeoxycholic acid (Item No. 10011286).{30823}  

     

    Brand:
    Cayman
    SKU:9002532 - 1 mg

    Available on backorder

  • Cholic acid 7-sulfate is a metabolite of the primary bile acid cholic acid (Item No. 20250).{30822,30823} It is produced by conjugation of a sulfate group with the hydroxy group at position 7 of cholic acid in the liver and gut. Fecal levels of cholic acid 7-sulfate are increased in male, but not female, mice fed a diet supplemented with cholic acid or chenodeoxycholic acid (Item No. 10011286).{30823}  

     

    Brand:
    Cayman
    SKU:9002532 - 10 mg

    Available on backorder

  • Cholic acid 7-sulfate is a metabolite of the primary bile acid cholic acid (Item No. 20250).{30822,30823} It is produced by conjugation of a sulfate group with the hydroxy group at position 7 of cholic acid in the liver and gut. Fecal levels of cholic acid 7-sulfate are increased in male, but not female, mice fed a diet supplemented with cholic acid or chenodeoxycholic acid (Item No. 10011286).{30823}  

     

    Brand:
    Cayman
    SKU:9002532 - 5 mg

    Available on backorder

  • Cholic acid 7-sulfate is a metabolite of the primary bile acid cholic acid (Item No. 20250).{30822,30823} It is produced by conjugation of a sulfate group with the hydroxy group at position 7 of cholic acid in the liver and gut. Fecal levels of cholic acid 7-sulfate are increased in male, but not female, mice fed a diet supplemented with cholic acid or chenodeoxycholic acid (Item No. 10011286).{30823}  

     

    Brand:
    Cayman
    SKU:9002532 - 500 µg

    Available on backorder

  • Cholic acid anilide is a synthetic bile acid and derivative of cholic acid (Item No. 20250) that inhibits the germination of C. difficile strain R20291 spores in vitro (IC50 = 1.8 μM).{44014}  

     

    Brand:
    Cayman
    SKU:26144 - 10 mg

    Available on backorder

  • Cholic acid anilide is a synthetic bile acid and derivative of cholic acid (Item No. 20250) that inhibits the germination of C. difficile strain R20291 spores in vitro (IC50 = 1.8 μM).{44014}  

     

    Brand:
    Cayman
    SKU:26144 - 25 mg

    Available on backorder

  • Cholic acid anilide is a synthetic bile acid and derivative of cholic acid (Item No. 20250) that inhibits the germination of C. difficile strain R20291 spores in vitro (IC50 = 1.8 μM).{44014}  

     

    Brand:
    Cayman
    SKU:26144 - 5 mg

    Available on backorder

  • Cholic acid anilide is a synthetic bile acid and derivative of cholic acid (Item No. 20250) that inhibits the germination of C. difficile strain R20291 spores in vitro (IC50 = 1.8 μM).{44014}  

     

    Brand:
    Cayman
    SKU:26144 - 50 mg

    Available on backorder

  • Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716} Cholic acid MaxSpec® standard is a quantitative grade standard of cholic acid (Item No. 20250) that has been prepared specifically for mass spectrometry and related applications where quantitative reproducibility is required. The solution has been prepared gravimetrically and is supplied in a deactivated glass ampule sealed under argon. The concentration was verified by comparison to an independently prepared calibration standard. This cholic acid MaxSpec® standard is guaranteed to meet identity, purity, stability, and concentration specifications and is provided with a batch-specific certificate of analysis. Ongoing stability testing is performed to ensure the concentration remains accurate throughout the shelf life of the product. Note: The amount of solution added to the vial is in excess of the listed amount. Therefore, it is necessary to accurately measure volumes for preparation of calibration standards. Follow recommended storage and handling conditions to maintain product quality.  

     

    Brand:
    Cayman
    SKU:31347 - 100 µg

    Available on backorder

  • Cholic acid-d4 contains four deuterium atoms at the 2, 2, 4, and 4 positions. It is intended for use as an internal standard for the quantification of cholic acid (Item No. 20250) by GC- or LC-MS. Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716}  

     

    Brand:
    Cayman
    SKU:20849 -

    Out of stock

  • Cholic acid-d4 contains four deuterium atoms at the 2, 2, 4, and 4 positions. It is intended for use as an internal standard for the quantification of cholic acid (Item No. 20250) by GC- or LC-MS. Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716}  

     

    Brand:
    Cayman
    SKU:20849 -

    Out of stock

  • Cholic acid-d4 contains four deuterium atoms at the 2, 2, 4, and 4 positions. It is intended for use as an internal standard for the quantification of cholic acid (Item No. 20250) by GC- or LC-MS. Cholic acid is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine to form bile salts.{30859} Cholic acid facilitates fat absorption and cholesterol excretion.{8343,29716}  

     

    Brand:
    Cayman
    SKU:20849 -

    Out of stock

  • Choline is an essential nutrient with roles in liver, neurological, hematological, and skeletal muscle homeostasis.{58015,58016,58014,58013} It is a precursor in the biosynthesis of membrane phospholipids, such as phosphatidylcholine, which facilitate cell signaling and transport across the membrane, and a precursor to the neurotransmitter acetylcholine. Choline is required for hepatic lipid transport.{58015} Perinatal administration of choline (18.8 mg/kg) improves prenatal alcohol exposure-induced cognitive deficits in rats.{58016} Choline (13 mg/animal per day) improves motor coordination and behavioral deficits in a mouse model of Rett syndrome, as well as improves deficits in recognition memory induced by early-life iron deficiency in rats when administered in the drinking water at a concentration of 5 ppm.{58014} Deficiencies in choline intake are positively correlated with muscle wasting, and dietary administration of choline (1,000 mg/kg) increases leg and breast muscle protein content in broiler chickens.{58013}  

     

    Brand:
    Cayman
    SKU:31178 - 100 g

    Available on backorder

  • Choline is an essential nutrient with roles in liver, neurological, hematological, and skeletal muscle homeostasis.{58015,58016,58014,58013} It is a precursor in the biosynthesis of membrane phospholipids, such as phosphatidylcholine, which facilitate cell signaling and transport across the membrane, and a precursor to the neurotransmitter acetylcholine. Choline is required for hepatic lipid transport.{58015} Perinatal administration of choline (18.8 mg/kg) improves prenatal alcohol exposure-induced cognitive deficits in rats.{58016} Choline (13 mg/animal per day) improves motor coordination and behavioral deficits in a mouse model of Rett syndrome, as well as improves deficits in recognition memory induced by early-life iron deficiency in rats when administered in the drinking water at a concentration of 5 ppm.{58014} Deficiencies in choline intake are positively correlated with muscle wasting, and dietary administration of choline (1,000 mg/kg) increases leg and breast muscle protein content in broiler chickens.{58013}  

     

    Brand:
    Cayman
    SKU:31178 - 250 g

    Available on backorder

  • Choline is an essential nutrient with roles in liver, neurological, hematological, and skeletal muscle homeostasis.{58015,58016,58014,58013} It is a precursor in the biosynthesis of membrane phospholipids, such as phosphatidylcholine, which facilitate cell signaling and transport across the membrane, and a precursor to the neurotransmitter acetylcholine. Choline is required for hepatic lipid transport.{58015} Perinatal administration of choline (18.8 mg/kg) improves prenatal alcohol exposure-induced cognitive deficits in rats.{58016} Choline (13 mg/animal per day) improves motor coordination and behavioral deficits in a mouse model of Rett syndrome, as well as improves deficits in recognition memory induced by early-life iron deficiency in rats when administered in the drinking water at a concentration of 5 ppm.{58014} Deficiencies in choline intake are positively correlated with muscle wasting, and dietary administration of choline (1,000 mg/kg) increases leg and breast muscle protein content in broiler chickens.{58013}  

     

    Brand:
    Cayman
    SKU:31178 - 50 g

    Available on backorder

  • Choline is an essential nutrient with roles in liver, neurological, hematological, and skeletal muscle homeostasis.{58015,58016,58014,58013} It is a precursor in the biosynthesis of membrane phospholipids, such as phosphatidylcholine, which facilitate cell signaling and transport across the membrane, and a precursor to the neurotransmitter acetylcholine. Choline is required for hepatic lipid transport.{58015} Perinatal administration of choline (18.8 mg/kg) improves prenatal alcohol exposure-induced cognitive deficits in rats.{58016} Choline (13 mg/animal per day) improves motor coordination and behavioral deficits in a mouse model of Rett syndrome, as well as improves deficits in recognition memory induced by early-life iron deficiency in rats when administered in the drinking water at a concentration of 5 ppm.{58014} Deficiencies in choline intake are positively correlated with muscle wasting, and dietary administration of choline (1,000 mg/kg) increases leg and breast muscle protein content in broiler chickens.{58013}  

     

    Brand:
    Cayman
    SKU:31178 - 500 g

    Available on backorder

  • CHR-6494 is a haspin protein kinase inhibitor (IC50 = 2 nM) selective over 27 other protein kinases, including Aurora B kinase (IC50 > 1 µM). Haspin is a kinase necessary for mitosis that selectively phosphorylates histone 3 at the threonine 3 residue (H3T3ph).{20471} CHR-6494 decreases phosphorylation of H3T3 and arrests the cell cycle in the G2/M phase, which leads to apoptosis. It showed promising results in a xenograft tumor model.  

     

    Brand:
    Cayman
    SKU:11478 - 1 mg

    Available on backorder

  • CHR-6494 is a haspin protein kinase inhibitor (IC50 = 2 nM) selective over 27 other protein kinases, including Aurora B kinase (IC50 > 1 µM). Haspin is a kinase necessary for mitosis that selectively phosphorylates histone 3 at the threonine 3 residue (H3T3ph).{20471} CHR-6494 decreases phosphorylation of H3T3 and arrests the cell cycle in the G2/M phase, which leads to apoptosis. It showed promising results in a xenograft tumor model.  

     

    Brand:
    Cayman
    SKU:11478 - 10 mg

    Available on backorder

  • CHR-6494 is a haspin protein kinase inhibitor (IC50 = 2 nM) selective over 27 other protein kinases, including Aurora B kinase (IC50 > 1 µM). Haspin is a kinase necessary for mitosis that selectively phosphorylates histone 3 at the threonine 3 residue (H3T3ph).{20471} CHR-6494 decreases phosphorylation of H3T3 and arrests the cell cycle in the G2/M phase, which leads to apoptosis. It showed promising results in a xenograft tumor model.  

     

    Brand:
    Cayman
    SKU:11478 - 5 mg

    Available on backorder

  • Chrodrimanin B is a meroterpenoid fungal metabolite that has been found in Talaromyces species.{48232} It has insecticidal activity against third instar silkworm larvae (LD50 = 10 μg/g of diet). Chrodrimanin B selectively inhibits the silkworm GABA receptor RDL (IC50 = 1.13 nM) over human α1β2γ2 subunit-containing GABA receptors (IC50 = 1.48 μM).{48233} The structure of thailandolide B, originally described as a C-9 epimer of chrodrimanin B, was revised in 2012 and is identical to that of chrodrimanin B.{48232}  

     

    Brand:
    Cayman
    SKU:27585 - 1 mg

    Available on backorder

  • Chromanol 293B is a blocker of slowly activating delayed-rectifier K+ current (IKs) with an IC50 value of 6.89 μM in Xenopus oocytes expressing rat IKs channels.{38238} It is selective, having no activity at rat Kv1.1 or Kir2.1 channels at a concentration of 30 μM. Chromanol 293B increases the rate and extent of IKs in guinea pig ventricular cells in a dose-dependent manner.{38239} It also inhibits cystic fibrosis transmembrane conductance regulator (CTFR) Cl- currents (ICTFR) with an IC50 value of 19 μM in Xenopus oocytes expressing human CTFR.{38240}  

     

    Brand:
    Cayman
    SKU:19993 -

    Available on backorder

  • Chromanol 293B is a blocker of slowly activating delayed-rectifier K+ current (IKs) with an IC50 value of 6.89 μM in Xenopus oocytes expressing rat IKs channels.{38238} It is selective, having no activity at rat Kv1.1 or Kir2.1 channels at a concentration of 30 μM. Chromanol 293B increases the rate and extent of IKs in guinea pig ventricular cells in a dose-dependent manner.{38239} It also inhibits cystic fibrosis transmembrane conductance regulator (CTFR) Cl- currents (ICTFR) with an IC50 value of 19 μM in Xenopus oocytes expressing human CTFR.{38240}  

     

    Brand:
    Cayman
    SKU:19993 -

    Available on backorder

  • Chromanol 293B is a blocker of slowly activating delayed-rectifier K+ current (IKs) with an IC50 value of 6.89 μM in Xenopus oocytes expressing rat IKs channels.{38238} It is selective, having no activity at rat Kv1.1 or Kir2.1 channels at a concentration of 30 μM. Chromanol 293B increases the rate and extent of IKs in guinea pig ventricular cells in a dose-dependent manner.{38239} It also inhibits cystic fibrosis transmembrane conductance regulator (CTFR) Cl- currents (ICTFR) with an IC50 value of 19 μM in Xenopus oocytes expressing human CTFR.{38240}  

     

    Brand:
    Cayman
    SKU:19993 -

    Available on backorder

  • Chromanol 293B is a blocker of slowly activating delayed-rectifier K+ current (IKs) with an IC50 value of 6.89 μM in Xenopus oocytes expressing rat IKs channels.{38238} It is selective, having no activity at rat Kv1.1 or Kir2.1 channels at a concentration of 30 μM. Chromanol 293B increases the rate and extent of IKs in guinea pig ventricular cells in a dose-dependent manner.{38239} It also inhibits cystic fibrosis transmembrane conductance regulator (CTFR) Cl- currents (ICTFR) with an IC50 value of 19 μM in Xenopus oocytes expressing human CTFR.{38240}  

     

    Brand:
    Cayman
    SKU:19993 -

    Available on backorder

  • Chromomycin A2 is an aureolic acid that has been found in several marine actinomycetes and has antibacterial and anticancer activities.{46145,46146} Chromomycin A2 inhibits the growth of B. subtilis in an agar diffusion assay.{46145} It also inhibits the growth of human SGC7901 gastric cancer, HepG2 hepatocellular carcinoma, A549 lung epithelial adenocarcinoma, HCT116 colon cancer, and COC1 ovarian cancer cells, as well as human umbilical vein endothelial cells (HUVECs; IC50s = 4, 0.5, 3, 5, 5, and 8 nM, respectively).{46146} Chromomycin A2 (30 nM) halts the cell cycle in the G0/G1 phase and increases the protein levels of LC3A and LC3B in MALME-3M melanoma cells, indicating that it induces autophagy.{46147} It also increases the levels and promoter activity of the autophagic proteins ATG7 and ATG10 and reduces cell viability to 50% in human SCC-11 squamous cell carcinoma cells when used at a concentration of 30 nM.{46148}  

     

    Brand:
    Cayman
    SKU:26954 - 1 mg

    Available on backorder

  • Chromomycin A2 is an aureolic acid that has been found in several marine actinomycetes and has antibacterial and anticancer activities.{46145,46146} Chromomycin A2 inhibits the growth of B. subtilis in an agar diffusion assay.{46145} It also inhibits the growth of human SGC7901 gastric cancer, HepG2 hepatocellular carcinoma, A549 lung epithelial adenocarcinoma, HCT116 colon cancer, and COC1 ovarian cancer cells, as well as human umbilical vein endothelial cells (HUVECs; IC50s = 4, 0.5, 3, 5, 5, and 8 nM, respectively).{46146} Chromomycin A2 (30 nM) halts the cell cycle in the G0/G1 phase and increases the protein levels of LC3A and LC3B in MALME-3M melanoma cells, indicating that it induces autophagy.{46147} It also increases the levels and promoter activity of the autophagic proteins ATG7 and ATG10 and reduces cell viability to 50% in human SCC-11 squamous cell carcinoma cells when used at a concentration of 30 nM.{46148}  

     

    Brand:
    Cayman
    SKU:26954 - 5 mg

    Available on backorder

  • Chromomycin A3 is an anthraquinone antibiotic and antitumor agent isolated from S. griseus that is used as a fluorescent probe for DNA with excitation/emission spectra of 445/575 nm.{36032,36035} Its DNA binding is specific to two or more contiguous GC base pairs, which makes it suitable for characterizing heterochromatin in plants with species-specific AT:GC ratios.{36035,36031} Chromomycin A3 is cytotoxic against non-small cell lung cancer and cervical cancer in vitro (IC50s = 1, 42, 60, and 40 nM for HCC44, A549, ME180, and HeLa cells, respectively).{366034,31081} It also inhibits oxidative stress- and DNA damage-induced neuronal injury by enhancing Sp1 and Sp3 transcription factor binding.{36033}  

     

    Brand:
    Cayman
    SKU:11315 - 1 mg

    Available on backorder

  • Chromomycin A3 is an anthraquinone antibiotic and antitumor agent isolated from S. griseus that is used as a fluorescent probe for DNA with excitation/emission spectra of 445/575 nm.{36032,36035} Its DNA binding is specific to two or more contiguous GC base pairs, which makes it suitable for characterizing heterochromatin in plants with species-specific AT:GC ratios.{36035,36031} Chromomycin A3 is cytotoxic against non-small cell lung cancer and cervical cancer in vitro (IC50s = 1, 42, 60, and 40 nM for HCC44, A549, ME180, and HeLa cells, respectively).{366034,31081} It also inhibits oxidative stress- and DNA damage-induced neuronal injury by enhancing Sp1 and Sp3 transcription factor binding.{36033}  

     

    Brand:
    Cayman
    SKU:11315 - 5 mg

    Available on backorder

  • Chrysin is a natural flavonoid with antioxidant, anti-inflammatory, and anticancer properties. It blocks COX-2 gene expression, PGE2 production, and hydroxyl radical formation in LPS-induced RAW 264.7 cells.{28408,28409} Chrysin inhibits insulin-induced HIF-1α expression (~50% at 10 µM) in human prostate cancer DU145 cells and blocks DU145 xenograft-induced angiogenesis in vivo.{28410} In a mouse model of ischemia/reperfusion injury, chrysin decreased pro-inflammatory gene expression and oxidative stress, resulting in a reduction of infarct volume and neurological defects.{28411}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Chrysin is a natural flavonoid with antioxidant, anti-inflammatory, and anticancer properties. It blocks COX-2 gene expression, PGE2 production, and hydroxyl radical formation in LPS-induced RAW 264.7 cells.{28408,28409} Chrysin inhibits insulin-induced HIF-1α expression (~50% at 10 µM) in human prostate cancer DU145 cells and blocks DU145 xenograft-induced angiogenesis in vivo.{28410} In a mouse model of ischemia/reperfusion injury, chrysin decreased pro-inflammatory gene expression and oxidative stress, resulting in a reduction of infarct volume and neurological defects.{28411}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Chrysin is a natural flavonoid with antioxidant, anti-inflammatory, and anticancer properties. It blocks COX-2 gene expression, PGE2 production, and hydroxyl radical formation in LPS-induced RAW 264.7 cells.{28408,28409} Chrysin inhibits insulin-induced HIF-1α expression (~50% at 10 µM) in human prostate cancer DU145 cells and blocks DU145 xenograft-induced angiogenesis in vivo.{28410} In a mouse model of ischemia/reperfusion injury, chrysin decreased pro-inflammatory gene expression and oxidative stress, resulting in a reduction of infarct volume and neurological defects.{28411}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Chrysin is a natural flavonoid with antioxidant, anti-inflammatory, and anticancer properties. It blocks COX-2 gene expression, PGE2 production, and hydroxyl radical formation in LPS-induced RAW 264.7 cells.{28408,28409} Chrysin inhibits insulin-induced HIF-1α expression (~50% at 10 µM) in human prostate cancer DU145 cells and blocks DU145 xenograft-induced angiogenesis in vivo.{28410} In a mouse model of ischemia/reperfusion injury, chrysin decreased pro-inflammatory gene expression and oxidative stress, resulting in a reduction of infarct volume and neurological defects.{28411}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Chrysomycin A is an antibiotic isolated from a strain of Streptomyces.{22201} It is structurally very similar to gilvocarcin V, an inhibitor of topoisomerase II which promotes DNA cross-linking with histone 3 and GRP78 when photoactivated by near-UV light.{22203,22198,22200} Chrysomycin A inhibits DNA synthesis in bacteria and suppresses the growth of transplantable tumors in mice.{22202,22199}  

     

    Brand:
    Cayman
    SKU:-
  • Chrysomycin A is an antibiotic isolated from a strain of Streptomyces.{22201} It is structurally very similar to gilvocarcin V, an inhibitor of topoisomerase II which promotes DNA cross-linking with histone 3 and GRP78 when photoactivated by near-UV light.{22203,22198,22200} Chrysomycin A inhibits DNA synthesis in bacteria and suppresses the growth of transplantable tumors in mice.{22202,22199}  

     

    Brand:
    Cayman
    SKU:-
  • Chrysomycin B is an antibiotic isolated from a strain of Streptomyces.{22201} It differs from its analog chrysomycin A (Item No. 14188){22203,22199} by having a methyl, rather than vinyl, group in the 8-position of the chromophore. Like its analog, chrysomycin B suppresses the growth of transplantable tumors in mice, an effect that may be related to its ability to bind DNA.{22199,22204,22198} It also causes DNA damage in the human lung adenocarcinoma A549 cell line and inhibits topoisomerase II.{22198} Chrysomycin B is structurally very similar to gilvocarcin V, which promotes DNA cross-linking with histone 3 and GRP78 when photoactivated by near-UV light.{22200}  

     

    Brand:
    Cayman
    SKU:-
  • Chrysomycin B is an antibiotic isolated from a strain of Streptomyces.{22201} It differs from its analog chrysomycin A (Item No. 14188){22203,22199} by having a methyl, rather than vinyl, group in the 8-position of the chromophore. Like its analog, chrysomycin B suppresses the growth of transplantable tumors in mice, an effect that may be related to its ability to bind DNA.{22199,22204,22198} It also causes DNA damage in the human lung adenocarcinoma A549 cell line and inhibits topoisomerase II.{22198} Chrysomycin B is structurally very similar to gilvocarcin V, which promotes DNA cross-linking with histone 3 and GRP78 when photoactivated by near-UV light.{22200}  

     

    Brand:
    Cayman
    SKU:-
  • Chrysophanol is an anthraquinone that has been found in R. palmatum and has diverse biological activities.{31786,31785,31784} It induces necrosis in J5 human liver cancer cells when used at concentrations of 25, 50, 75, 100, and 200 µM.{31785} Chrysophanol (5, 10, and 50 µM) reduces LPS-induced production of nitric oxide (NO) and prostaglandin E2 (PGE2; Item No. 14010) and inhibits LPS-induced DNA oxidation in BV-2 microglia.{31784} In vivo, chrysophanol (5 mg/kg) decreases colonic levels of IL-6 and activation of NF-κB and reduces weight loss, diarrhea, and rectal bleeding in a mouse model of colitis induced by dextran sulfate (DSS; Item No. 23250).{59380} Chrysophanol (0.1, 1, and 10 mg/kg) increases survival, reduces brain tissue loss, and ameliorates motor balance deficits in a mouse model of ischemia-reperfusion injury induced by middle cerebral artery occlusion (MCAO).{59381}  

     

    Brand:
    Cayman
    SKU:19870 -

    Available on backorder

  • Chrysophanol is an anthraquinone that has been found in R. palmatum and has diverse biological activities.{31786,31785,31784} It induces necrosis in J5 human liver cancer cells when used at concentrations of 25, 50, 75, 100, and 200 µM.{31785} Chrysophanol (5, 10, and 50 µM) reduces LPS-induced production of nitric oxide (NO) and prostaglandin E2 (PGE2; Item No. 14010) and inhibits LPS-induced DNA oxidation in BV-2 microglia.{31784} In vivo, chrysophanol (5 mg/kg) decreases colonic levels of IL-6 and activation of NF-κB and reduces weight loss, diarrhea, and rectal bleeding in a mouse model of colitis induced by dextran sulfate (DSS; Item No. 23250).{59380} Chrysophanol (0.1, 1, and 10 mg/kg) increases survival, reduces brain tissue loss, and ameliorates motor balance deficits in a mouse model of ischemia-reperfusion injury induced by middle cerebral artery occlusion (MCAO).{59381}  

     

    Brand:
    Cayman
    SKU:19870 -

    Available on backorder

  • Chrysophanol is an anthraquinone that has been found in R. palmatum and has diverse biological activities.{31786,31785,31784} It induces necrosis in J5 human liver cancer cells when used at concentrations of 25, 50, 75, 100, and 200 µM.{31785} Chrysophanol (5, 10, and 50 µM) reduces LPS-induced production of nitric oxide (NO) and prostaglandin E2 (PGE2; Item No. 14010) and inhibits LPS-induced DNA oxidation in BV-2 microglia.{31784} In vivo, chrysophanol (5 mg/kg) decreases colonic levels of IL-6 and activation of NF-κB and reduces weight loss, diarrhea, and rectal bleeding in a mouse model of colitis induced by dextran sulfate (DSS; Item No. 23250).{59380} Chrysophanol (0.1, 1, and 10 mg/kg) increases survival, reduces brain tissue loss, and ameliorates motor balance deficits in a mouse model of ischemia-reperfusion injury induced by middle cerebral artery occlusion (MCAO).{59381}  

     

    Brand:
    Cayman
    SKU:19870 -

    Available on backorder

  • Chrysosplenetin is a flavonoid that has been found in A. annua and has diverse biological activities.{57215,57216,57217} It is active against P. falciparum in vitro (IC50 = 23 µM).{57215} Chrysosplenetin inhibits the cytopathic effect of enterovirus 71 (EV71) in Vero cells (EC50 = 0.68 µM) and increases survival in a neonatal mouse model of EV71 infection when administered at doses of 1 and 5 mg/kg.{57216} It also increases proliferation and osteogenic differentiation of isolated human bone marrow stromal cells (BMSCs) and prevents estrogen deficiency-induced bone loss in ovariectomized mice.{57217}  

     

    Brand:
    Cayman
    SKU:30625 - 1 mg

    Available on backorder

  • Chrysosplenetin is a flavonoid that has been found in A. annua and has diverse biological activities.{57215,57216,57217} It is active against P. falciparum in vitro (IC50 = 23 µM).{57215} Chrysosplenetin inhibits the cytopathic effect of enterovirus 71 (EV71) in Vero cells (EC50 = 0.68 µM) and increases survival in a neonatal mouse model of EV71 infection when administered at doses of 1 and 5 mg/kg.{57216} It also increases proliferation and osteogenic differentiation of isolated human bone marrow stromal cells (BMSCs) and prevents estrogen deficiency-induced bone loss in ovariectomized mice.{57217}  

     

    Brand:
    Cayman
    SKU:30625 - 10 mg

    Available on backorder

  • Chrysosplenetin is a flavonoid that has been found in A. annua and has diverse biological activities.{57215,57216,57217} It is active against P. falciparum in vitro (IC50 = 23 µM).{57215} Chrysosplenetin inhibits the cytopathic effect of enterovirus 71 (EV71) in Vero cells (EC50 = 0.68 µM) and increases survival in a neonatal mouse model of EV71 infection when administered at doses of 1 and 5 mg/kg.{57216} It also increases proliferation and osteogenic differentiation of isolated human bone marrow stromal cells (BMSCs) and prevents estrogen deficiency-induced bone loss in ovariectomized mice.{57217}  

     

    Brand:
    Cayman
    SKU:30625 - 5 mg

    Available on backorder

  • CHS-828 is a pyridyl cyanoguanidine anti-tumor agent that has been identified as a competitive inhibitor of Nampt as well as an inhibitor of NF-κB pathway activity.{20745,20747} CHS-828 has potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.5 nM) cells both in vitro and in vivo.{20744} In nude mice bearing human tumor xenografts, CHS-828, at 20-50 mg/kg/day, inhibits the growth of MCF-7 breast cancer tumors and induces regression of NYH small cell lung cancer tumors.{20744}  

     

    Brand:
    Cayman
    SKU:11021 - 10 mg

    Available on backorder

  • CHS-828 is a pyridyl cyanoguanidine anti-tumor agent that has been identified as a competitive inhibitor of Nampt as well as an inhibitor of NF-κB pathway activity.{20745,20747} CHS-828 has potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.5 nM) cells both in vitro and in vivo.{20744} In nude mice bearing human tumor xenografts, CHS-828, at 20-50 mg/kg/day, inhibits the growth of MCF-7 breast cancer tumors and induces regression of NYH small cell lung cancer tumors.{20744}  

     

    Brand:
    Cayman
    SKU:11021 - 25 mg

    Available on backorder

  • CHS-828 is a pyridyl cyanoguanidine anti-tumor agent that has been identified as a competitive inhibitor of Nampt as well as an inhibitor of NF-κB pathway activity.{20745,20747} CHS-828 has potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.5 nM) cells both in vitro and in vivo.{20744} In nude mice bearing human tumor xenografts, CHS-828, at 20-50 mg/kg/day, inhibits the growth of MCF-7 breast cancer tumors and induces regression of NYH small cell lung cancer tumors.{20744}  

     

    Brand:
    Cayman
    SKU:11021 - 5 mg

    Available on backorder

  • CHS-828 is a pyridyl cyanoguanidine anti-tumor agent that has been identified as a competitive inhibitor of Nampt as well as an inhibitor of NF-κB pathway activity.{20745,20747} CHS-828 has potent cytotoxic effects in human breast (IC50 = 7.3 nM) and lung cancer (IC50 = 0.5 nM) cells both in vitro and in vivo.{20744} In nude mice bearing human tumor xenografts, CHS-828, at 20-50 mg/kg/day, inhibits the growth of MCF-7 breast cancer tumors and induces regression of NYH small cell lung cancer tumors.{20744}  

     

    Brand:
    Cayman
    SKU:11021 - 50 mg

    Available on backorder

  • Chymostatin is a bioactive peptide of microbial origin that acts as a protease inhibitor with selectivity for chymotryptase-like serine proteases.{24067} It potently inhibits chymotrypsin and chymase (Ki = 9.36 and 13.1 nM, respectively) while less effectively blocking the activity of cathepsins, papain, and leukocyte elastase.{24069,24067,24065,24068,24066} It is without effect on trypsin, thrombin, plasmin, pepsin, and kallikrein.{24067}  

     

    Brand:
    Cayman
    SKU:-
  • Chymostatin is a bioactive peptide of microbial origin that acts as a protease inhibitor with selectivity for chymotryptase-like serine proteases.{24067} It potently inhibits chymotrypsin and chymase (Ki = 9.36 and 13.1 nM, respectively) while less effectively blocking the activity of cathepsins, papain, and leukocyte elastase.{24069,24067,24065,24068,24066} It is without effect on trypsin, thrombin, plasmin, pepsin, and kallikrein.{24067}  

     

    Brand:
    Cayman
    SKU:-
  • Chymostatin is a bioactive peptide of microbial origin that acts as a protease inhibitor with selectivity for chymotryptase-like serine proteases.{24067} It potently inhibits chymotrypsin and chymase (Ki = 9.36 and 13.1 nM, respectively) while less effectively blocking the activity of cathepsins, papain, and leukocyte elastase.{24069,24067,24065,24068,24066} It is without effect on trypsin, thrombin, plasmin, pepsin, and kallikrein.{24067}  

     

    Brand:
    Cayman
    SKU:-
  • Chymostatin is a bioactive peptide of microbial origin that acts as a protease inhibitor with selectivity for chymotryptase-like serine proteases.{24067} It potently inhibits chymotrypsin and chymase (Ki = 9.36 and 13.1 nM, respectively) while less effectively blocking the activity of cathepsins, papain, and leukocyte elastase.{24069,24067,24065,24068,24066} It is without effect on trypsin, thrombin, plasmin, pepsin, and kallikrein.{24067}  

     

    Brand:
    Cayman
    SKU:-
  • The dual specific threonine/tyrosine kinase, map kinase kinase (MEK), is a key component of the RAS/RAF/MEK/ERK signaling pathway that is frequently activated in human tumors.{6694,16830} CI-1040 is a benzhydroxamate compound that potently inhibits MEK in an in vitro mitogen-activated protein kinase cascade assay with an IC50 value of 2.3 nM (Kd = 74 nM when activated with adenosine triphosphate).{16877,15629} It can suppress phosphorylation of ERK in mouse colon 26 tumors with an IC50 value of 35 nM and demonstrates in vivo activity with oral administration in a mouse tumor model.{16877} The second-generation MEK inhibitor PD 0325901 (Item No. 13034) is a structural derivative of CI-1040 that was developed for improved solubility.{16877}  

     

    Brand:
    Cayman
    SKU:11580 - 10 mg

    Available on backorder

  • The dual specific threonine/tyrosine kinase, map kinase kinase (MEK), is a key component of the RAS/RAF/MEK/ERK signaling pathway that is frequently activated in human tumors.{6694,16830} CI-1040 is a benzhydroxamate compound that potently inhibits MEK in an in vitro mitogen-activated protein kinase cascade assay with an IC50 value of 2.3 nM (Kd = 74 nM when activated with adenosine triphosphate).{16877,15629} It can suppress phosphorylation of ERK in mouse colon 26 tumors with an IC50 value of 35 nM and demonstrates in vivo activity with oral administration in a mouse tumor model.{16877} The second-generation MEK inhibitor PD 0325901 (Item No. 13034) is a structural derivative of CI-1040 that was developed for improved solubility.{16877}  

     

    Brand:
    Cayman
    SKU:11580 - 25 mg

    Available on backorder

  • The dual specific threonine/tyrosine kinase, map kinase kinase (MEK), is a key component of the RAS/RAF/MEK/ERK signaling pathway that is frequently activated in human tumors.{6694,16830} CI-1040 is a benzhydroxamate compound that potently inhibits MEK in an in vitro mitogen-activated protein kinase cascade assay with an IC50 value of 2.3 nM (Kd = 74 nM when activated with adenosine triphosphate).{16877,15629} It can suppress phosphorylation of ERK in mouse colon 26 tumors with an IC50 value of 35 nM and demonstrates in vivo activity with oral administration in a mouse tumor model.{16877} The second-generation MEK inhibitor PD 0325901 (Item No. 13034) is a structural derivative of CI-1040 that was developed for improved solubility.{16877}  

     

    Brand:
    Cayman
    SKU:11580 - 5 mg

    Available on backorder

  • The dual specific threonine/tyrosine kinase, map kinase kinase (MEK), is a key component of the RAS/RAF/MEK/ERK signaling pathway that is frequently activated in human tumors.{6694,16830} CI-1040 is a benzhydroxamate compound that potently inhibits MEK in an in vitro mitogen-activated protein kinase cascade assay with an IC50 value of 2.3 nM (Kd = 74 nM when activated with adenosine triphosphate).{16877,15629} It can suppress phosphorylation of ERK in mouse colon 26 tumors with an IC50 value of 35 nM and demonstrates in vivo activity with oral administration in a mouse tumor model.{16877} The second-generation MEK inhibitor PD 0325901 (Item No. 13034) is a structural derivative of CI-1040 that was developed for improved solubility.{16877}  

     

    Brand:
    Cayman
    SKU:11580 - 50 mg

    Available on backorder

  • Acyl-coenzyme A:cholesterol acyltransferase 1 (ACAT-1) is a sterol O-acyltransferase that catalyzes the formation of fatty acid-cholesterol esters, an important step in lipoprotein assembly and dietary cholesterol absorption.{12931,12021} CI-976 is a potent, selective inhibitor of ACAT-1 (IC50 = 73 nM).{28323,28321} It is orally bioavailable and decreases plasma total cholesterol, very low density lipoprotein (VLDL) cholesterol, LDL cholesterol, apolipoprotein B, liver cholesteryl esters, and VLDL and LDL cholesteryl ester content in rabbits given a diet that induces hypercholesterolemia.{28322} CI-976 also diminishes atherosclerotic activity in hypercholesterolemic rabbits.{28324}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Acyl-coenzyme A:cholesterol acyltransferase 1 (ACAT-1) is a sterol O-acyltransferase that catalyzes the formation of fatty acid-cholesterol esters, an important step in lipoprotein assembly and dietary cholesterol absorption.{12931,12021} CI-976 is a potent, selective inhibitor of ACAT-1 (IC50 = 73 nM).{28323,28321} It is orally bioavailable and decreases plasma total cholesterol, very low density lipoprotein (VLDL) cholesterol, LDL cholesterol, apolipoprotein B, liver cholesteryl esters, and VLDL and LDL cholesteryl ester content in rabbits given a diet that induces hypercholesterolemia.{28322} CI-976 also diminishes atherosclerotic activity in hypercholesterolemic rabbits.{28324}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Acyl-coenzyme A:cholesterol acyltransferase 1 (ACAT-1) is a sterol O-acyltransferase that catalyzes the formation of fatty acid-cholesterol esters, an important step in lipoprotein assembly and dietary cholesterol absorption.{12931,12021} CI-976 is a potent, selective inhibitor of ACAT-1 (IC50 = 73 nM).{28323,28321} It is orally bioavailable and decreases plasma total cholesterol, very low density lipoprotein (VLDL) cholesterol, LDL cholesterol, apolipoprotein B, liver cholesteryl esters, and VLDL and LDL cholesteryl ester content in rabbits given a diet that induces hypercholesterolemia.{28322} CI-976 also diminishes atherosclerotic activity in hypercholesterolemic rabbits.{28324}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Acyl-coenzyme A:cholesterol acyltransferase 1 (ACAT-1) is a sterol O-acyltransferase that catalyzes the formation of fatty acid-cholesterol esters, an important step in lipoprotein assembly and dietary cholesterol absorption.{12931,12021} CI-976 is a potent, selective inhibitor of ACAT-1 (IC50 = 73 nM).{28323,28321} It is orally bioavailable and decreases plasma total cholesterol, very low density lipoprotein (VLDL) cholesterol, LDL cholesterol, apolipoprotein B, liver cholesteryl esters, and VLDL and LDL cholesteryl ester content in rabbits given a diet that induces hypercholesterolemia.{28322} CI-976 also diminishes atherosclerotic activity in hypercholesterolemic rabbits.{28324}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • CI-994 is an inhibitor of class I HDACs displaying IC50 values of 0.9, 0.9, 1.2, and >20 μM when screened in vitro against recombinant human HDAC 1, 2, 3, and 8, respectively.{21578} CI-994 has a wide spectrum of antitumor activity, particularly in tumors normally refractory to conventional anticancer agents, in preclinical models both in vitro and in vivo and has advanced through phase I and II clinical trials in combination therapy treatments.{21576,21577,21579}  

     

    Brand:
    Cayman
    SKU:12084 - 10 mg

    Available on backorder

  • CI-994 is an inhibitor of class I HDACs displaying IC50 values of 0.9, 0.9, 1.2, and >20 μM when screened in vitro against recombinant human HDAC 1, 2, 3, and 8, respectively.{21578} CI-994 has a wide spectrum of antitumor activity, particularly in tumors normally refractory to conventional anticancer agents, in preclinical models both in vitro and in vivo and has advanced through phase I and II clinical trials in combination therapy treatments.{21576,21577,21579}  

     

    Brand:
    Cayman
    SKU:12084 - 5 mg

    Available on backorder

  • CI-994 is an inhibitor of class I HDACs displaying IC50 values of 0.9, 0.9, 1.2, and >20 μM when screened in vitro against recombinant human HDAC 1, 2, 3, and 8, respectively.{21578} CI-994 has a wide spectrum of antitumor activity, particularly in tumors normally refractory to conventional anticancer agents, in preclinical models both in vitro and in vivo and has advanced through phase I and II clinical trials in combination therapy treatments.{21576,21577,21579}  

     

    Brand:
    Cayman
    SKU:12084 - 50 mg

    Available on backorder

  • Prostaglandin I2 (PGI2, prostacyclin) is the most potent endogenous vasodilator that affects both the systemic and pulmonary circulation.{643} Cicaprost is a PGI2 analog that is orally active with prolonged availability in vivo, having a terminal half life in plasma of one hour.{6640}{18554} In addition to their effects on smooth muscle, PGI2 analogs, including cicaprost, have been shown to inhibit the pro-inflammatory actions of certain leukocytes, suppress cardiac fibrosis, and block mitogenesis of certain cell types.{18547}{18548}{18546} Importantly, cicaprost has been shown to strongly reduce lung and lymph node metastasis in rats, suggesting that it might be useful in cancer therapy.{19177}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Prostaglandin I2 (PGI2, prostacyclin) is the most potent endogenous vasodilator that affects both the systemic and pulmonary circulation.{643} Cicaprost is a PGI2 analog that is orally active with prolonged availability in vivo, having a terminal half life in plasma of one hour.{6640}{18554} In addition to their effects on smooth muscle, PGI2 analogs, including cicaprost, have been shown to inhibit the pro-inflammatory actions of certain leukocytes, suppress cardiac fibrosis, and block mitogenesis of certain cell types.{18547}{18548}{18546} Importantly, cicaprost has been shown to strongly reduce lung and lymph node metastasis in rats, suggesting that it might be useful in cancer therapy.{19177}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Prostaglandin I2 (PGI2, prostacyclin) is the most potent endogenous vasodilator that affects both the systemic and pulmonary circulation.{643} Cicaprost is a PGI2 analog that is orally active with prolonged availability in vivo, having a terminal half life in plasma of one hour.{6640}{18554} In addition to their effects on smooth muscle, PGI2 analogs, including cicaprost, have been shown to inhibit the pro-inflammatory actions of certain leukocytes, suppress cardiac fibrosis, and block mitogenesis of certain cell types.{18547}{18548}{18546} Importantly, cicaprost has been shown to strongly reduce lung and lymph node metastasis in rats, suggesting that it might be useful in cancer therapy.{19177}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Ciclesonide (CIC) is a prodrug form of the glucocorticoid receptor agonist desisobutyryl-CIC (des-CIC).{29504} CIC binds to the glucocorticoid receptor with a Ki value of 37 nM.{29502} It is selective for the glucocorticoid receptor over the estrogen, progesterone, and testosterone receptors. CIC inhibits eosinophil influx into the lung (ED50 = 0.49 mg/kg) and reduces sephadex-induced lung edema (ED50 = 0.72 mg/kg) in a rat model of ovalbumin-sensitized and -challenged airway inflammation. Formulations containing CIC have been used in the maintenance treatment of asthma and in the treatment of allergic rhinitis.  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Ciclesonide (CIC) is a prodrug form of the glucocorticoid receptor agonist desisobutyryl-CIC (des-CIC).{29504} CIC binds to the glucocorticoid receptor with a Ki value of 37 nM.{29502} It is selective for the glucocorticoid receptor over the estrogen, progesterone, and testosterone receptors. CIC inhibits eosinophil influx into the lung (ED50 = 0.49 mg/kg) and reduces sephadex-induced lung edema (ED50 = 0.72 mg/kg) in a rat model of ovalbumin-sensitized and -challenged airway inflammation. Formulations containing CIC have been used in the maintenance treatment of asthma and in the treatment of allergic rhinitis.  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Ciclesonide (CIC) is a prodrug form of the glucocorticoid receptor agonist desisobutyryl-CIC (des-CIC).{29504} CIC binds to the glucocorticoid receptor with a Ki value of 37 nM.{29502} It is selective for the glucocorticoid receptor over the estrogen, progesterone, and testosterone receptors. CIC inhibits eosinophil influx into the lung (ED50 = 0.49 mg/kg) and reduces sephadex-induced lung edema (ED50 = 0.72 mg/kg) in a rat model of ovalbumin-sensitized and -challenged airway inflammation. Formulations containing CIC have been used in the maintenance treatment of asthma and in the treatment of allergic rhinitis.  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Ciclesonide (CIC) is a prodrug form of the glucocorticoid receptor agonist desisobutyryl-CIC (des-CIC).{29504} CIC binds to the glucocorticoid receptor with a Ki value of 37 nM.{29502} It is selective for the glucocorticoid receptor over the estrogen, progesterone, and testosterone receptors. CIC inhibits eosinophil influx into the lung (ED50 = 0.49 mg/kg) and reduces sephadex-induced lung edema (ED50 = 0.72 mg/kg) in a rat model of ovalbumin-sensitized and -challenged airway inflammation. Formulations containing CIC have been used in the maintenance treatment of asthma and in the treatment of allergic rhinitis.  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Ciclesonide-d7 is intended for use as an internal standard for the quantification of ciclesonide (CIC; Item No. 18227) by GC- or LC-MS. Ciclesonide is a prodrug form of the glucocorticoid receptor agonist desisobutyryl-CIC (des-CIC).{29504} CIC binds to the glucocorticoid receptor with a Ki value of 37 nM.{29502} It is selective for the glucocorticoid receptor over the estrogen, progesterone, and testosterone receptors. CIC inhibits eosinophil influx into the lung (ED50 = 0.49 mg/kg) and reduces sephadex-induced lung edema (ED50 = 0.72 mg/kg) in a rat model of ovalbumin-sensitized and -challenged airway inflammation. Formulations containing CIC have been used in the maintenance treatment of asthma and in the treatment of allergic rhinitis.  

     

    Brand:
    Cayman
    SKU:28527 - 1 mg

    Available on backorder

  • Ciclesonide-d7 is intended for use as an internal standard for the quantification of ciclesonide (CIC; Item No. 18227) by GC- or LC-MS. Ciclesonide is a prodrug form of the glucocorticoid receptor agonist desisobutyryl-CIC (des-CIC).{29504} CIC binds to the glucocorticoid receptor with a Ki value of 37 nM.{29502} It is selective for the glucocorticoid receptor over the estrogen, progesterone, and testosterone receptors. CIC inhibits eosinophil influx into the lung (ED50 = 0.49 mg/kg) and reduces sephadex-induced lung edema (ED50 = 0.72 mg/kg) in a rat model of ovalbumin-sensitized and -challenged airway inflammation. Formulations containing CIC have been used in the maintenance treatment of asthma and in the treatment of allergic rhinitis.  

     

    Brand:
    Cayman
    SKU:28527 - 500 µg

    Available on backorder

  • Ciclopirox is an iron chelator, antifungal, and anticancer agent.{26941,41490,53131,53132} It inhibits the iron-dependent enzyme prolyl hydroxylase 2 (PHD2; IC50 = 1.58 μM), an effect that is reduced in the presence of iron.{26941} It stabilizes hypoxia-inducible factor-α (HIF-1α) under normoxic conditions in rat glomus cells when used at a concentration of 5 μM.{33213} Ciclopirox is active against clinical isolates of T. rubrum, T. mentagrophytes, and C. albicans (MICs = 0.03-0.5, 0.03-0.5, and 0.06-0.5 μg/ml, respectively) and inhibits growth of T. mentagrophytes on porcine skin ex vivo when applied topically.{41490,53131} It inhibits proliferation of Rh30, HT-29, and MDA-MB-231 cells in a concentration-dependent manner and halts the cell cycle at the G1/G0 phase and induces apoptosis in Rh30 cells.{53132} Ciclopirox (25 mg/kg) reduces tumor growth in an MDA-MB-231 mouse xenograft model. Formulations containing ciclopirox have been used in the topical treatment of fungal infections.  

     

    Brand:
    Cayman
    SKU:-
  • Ciclopirox is an iron chelator, antifungal, and anticancer agent.{26941,41490,53131,53132} It inhibits the iron-dependent enzyme prolyl hydroxylase 2 (PHD2; IC50 = 1.58 μM), an effect that is reduced in the presence of iron.{26941} It stabilizes hypoxia-inducible factor-α (HIF-1α) under normoxic conditions in rat glomus cells when used at a concentration of 5 μM.{33213} Ciclopirox is active against clinical isolates of T. rubrum, T. mentagrophytes, and C. albicans (MICs = 0.03-0.5, 0.03-0.5, and 0.06-0.5 μg/ml, respectively) and inhibits growth of T. mentagrophytes on porcine skin ex vivo when applied topically.{41490,53131} It inhibits proliferation of Rh30, HT-29, and MDA-MB-231 cells in a concentration-dependent manner and halts the cell cycle at the G1/G0 phase and induces apoptosis in Rh30 cells.{53132} Ciclopirox (25 mg/kg) reduces tumor growth in an MDA-MB-231 mouse xenograft model. Formulations containing ciclopirox have been used in the topical treatment of fungal infections.  

     

    Brand:
    Cayman
    SKU:-
  • Ciclopirox is an iron chelator, antifungal, and anticancer agent.{26941,41490,53131,53132} It inhibits the iron-dependent enzyme prolyl hydroxylase 2 (PHD2; IC50 = 1.58 μM), an effect that is reduced in the presence of iron.{26941} It stabilizes hypoxia-inducible factor-α (HIF-1α) under normoxic conditions in rat glomus cells when used at a concentration of 5 μM.{33213} Ciclopirox is active against clinical isolates of T. rubrum, T. mentagrophytes, and C. albicans (MICs = 0.03-0.5, 0.03-0.5, and 0.06-0.5 μg/ml, respectively) and inhibits growth of T. mentagrophytes on porcine skin ex vivo when applied topically.{41490,53131} It inhibits proliferation of Rh30, HT-29, and MDA-MB-231 cells in a concentration-dependent manner and halts the cell cycle at the G1/G0 phase and induces apoptosis in Rh30 cells.{53132} Ciclopirox (25 mg/kg) reduces tumor growth in an MDA-MB-231 mouse xenograft model. Formulations containing ciclopirox have been used in the topical treatment of fungal infections.  

     

    Brand:
    Cayman
    SKU:-
  • Ciclopirox is an iron chelator, antifungal, and anticancer agent.{26941,41490,53131,53132} It inhibits the iron-dependent enzyme prolyl hydroxylase 2 (PHD2; IC50 = 1.58 μM), an effect that is reduced in the presence of iron.{26941} It stabilizes hypoxia-inducible factor-α (HIF-1α) under normoxic conditions in rat glomus cells when used at a concentration of 5 μM.{33213} Ciclopirox is active against clinical isolates of T. rubrum, T. mentagrophytes, and C. albicans (MICs = 0.03-0.5, 0.03-0.5, and 0.06-0.5 μg/ml, respectively) and inhibits growth of T. mentagrophytes on porcine skin ex vivo when applied topically.{41490,53131} It inhibits proliferation of Rh30, HT-29, and MDA-MB-231 cells in a concentration-dependent manner and halts the cell cycle at the G1/G0 phase and induces apoptosis in Rh30 cells.{53132} Ciclopirox (25 mg/kg) reduces tumor growth in an MDA-MB-231 mouse xenograft model. Formulations containing ciclopirox have been used in the topical treatment of fungal infections.  

     

    Brand:
    Cayman
    SKU:-
  • The Ras family of GTPases, including the Arf, Rho, Ras, and Rab GTPase subfamilies, regulates various cellular processes ranging from membrane trafficking to the control of cell proliferation. They regulate cell physiology by switching between active and inactive conformational states by binding either GTP or GDP. Alterations in GTPase function are a known hallmark of certain cancers and genetic diseases. CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases.{24538} It binds the nucleotide binding pocket of Rab7 with a Ki value of 13 nM, preventing BODIPY-linked GTP and GDP binding with EC50 values of 11.2 and 21 nM, respectively.{24538}  

     

    Brand:
    Cayman
    SKU:-
  • The Ras family of GTPases, including the Arf, Rho, Ras, and Rab GTPase subfamilies, regulates various cellular processes ranging from membrane trafficking to the control of cell proliferation. They regulate cell physiology by switching between active and inactive conformational states by binding either GTP or GDP. Alterations in GTPase function are a known hallmark of certain cancers and genetic diseases. CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases.{24538} It binds the nucleotide binding pocket of Rab7 with a Ki value of 13 nM, preventing BODIPY-linked GTP and GDP binding with EC50 values of 11.2 and 21 nM, respectively.{24538}  

     

    Brand:
    Cayman
    SKU:-
  • The Ras family of GTPases, including the Arf, Rho, Ras, and Rab GTPase subfamilies, regulates various cellular processes ranging from membrane trafficking to the control of cell proliferation. They regulate cell physiology by switching between active and inactive conformational states by binding either GTP or GDP. Alterations in GTPase function are a known hallmark of certain cancers and genetic diseases. CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases.{24538} It binds the nucleotide binding pocket of Rab7 with a Ki value of 13 nM, preventing BODIPY-linked GTP and GDP binding with EC50 values of 11.2 and 21 nM, respectively.{24538}  

     

    Brand:
    Cayman
    SKU:-
  • The Ras family of GTPases, including the Arf, Rho, Ras, and Rab GTPase subfamilies, regulates various cellular processes ranging from membrane trafficking to the control of cell proliferation. They regulate cell physiology by switching between active and inactive conformational states by binding either GTP or GDP. Alterations in GTPase function are a known hallmark of certain cancers and genetic diseases. CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases.{24538} It binds the nucleotide binding pocket of Rab7 with a Ki value of 13 nM, preventing BODIPY-linked GTP and GDP binding with EC50 values of 11.2 and 21 nM, respectively.{24538}  

     

    Brand:
    Cayman
    SKU:-
  • CID-1375606 is a GPR27 agonist with EC50 values of 0.46 µM and 7.9 µM in chimeric GPR27V2 and wild-type GPR27 luciferase β-arrestin-2 complementation assays, respectively.{54081} It is selective for GPR27 over the closely related receptors GPR85 and GPR173 for which it does not induce β-arrestin-2 recruitment in the same assay. GPR27 function has been linked to insulin promoter activity and excretion.{54082}  

     

    Brand:
    Cayman
    SKU:30422 - 10 mg

    Available on backorder

  • CID-1375606 is a GPR27 agonist with EC50 values of 0.46 µM and 7.9 µM in chimeric GPR27V2 and wild-type GPR27 luciferase β-arrestin-2 complementation assays, respectively.{54081} It is selective for GPR27 over the closely related receptors GPR85 and GPR173 for which it does not induce β-arrestin-2 recruitment in the same assay. GPR27 function has been linked to insulin promoter activity and excretion.{54082}  

     

    Brand:
    Cayman
    SKU:30422 - 25 mg

    Available on backorder

  • CID-1375606 is a GPR27 agonist with EC50 values of 0.46 µM and 7.9 µM in chimeric GPR27V2 and wild-type GPR27 luciferase β-arrestin-2 complementation assays, respectively.{54081} It is selective for GPR27 over the closely related receptors GPR85 and GPR173 for which it does not induce β-arrestin-2 recruitment in the same assay. GPR27 function has been linked to insulin promoter activity and excretion.{54082}  

     

    Brand:
    Cayman
    SKU:30422 - 5 mg

    Available on backorder

  • Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by diacylglycerol, commonly downstream of PKC signaling.{13335} The three human PKD isoforms target a variety of proteins to alter cell proliferation, survival, invasion, and protein transport.{13335,25032} CID-2011756 is an inhibitor of all three PKD isoforms (IC50s = 3.2, 0.6, and 0.7 μM for PKD1, PKD2, and PKD3, respectively).{25032} This ATP-competitive inhibitor is cell permeable, blocking the phosphorylation of PKD1 on Ser916 (an autocatalytic target) in LNCaP prostate cancer cells in response to phorbol esters (EC50 = 10 μM).{25032}  

     

    Brand:
    Cayman
    SKU:-
  • Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by diacylglycerol, commonly downstream of PKC signaling.{13335} The three human PKD isoforms target a variety of proteins to alter cell proliferation, survival, invasion, and protein transport.{13335,25032} CID-2011756 is an inhibitor of all three PKD isoforms (IC50s = 3.2, 0.6, and 0.7 μM for PKD1, PKD2, and PKD3, respectively).{25032} This ATP-competitive inhibitor is cell permeable, blocking the phosphorylation of PKD1 on Ser916 (an autocatalytic target) in LNCaP prostate cancer cells in response to phorbol esters (EC50 = 10 μM).{25032}  

     

    Brand:
    Cayman
    SKU:-
  • Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by diacylglycerol, commonly downstream of PKC signaling.{13335} The three human PKD isoforms target a variety of proteins to alter cell proliferation, survival, invasion, and protein transport.{13335,25032} CID-2011756 is an inhibitor of all three PKD isoforms (IC50s = 3.2, 0.6, and 0.7 μM for PKD1, PKD2, and PKD3, respectively).{25032} This ATP-competitive inhibitor is cell permeable, blocking the phosphorylation of PKD1 on Ser916 (an autocatalytic target) in LNCaP prostate cancer cells in response to phorbol esters (EC50 = 10 μM).{25032}  

     

    Brand:
    Cayman
    SKU:-
  • GPR35 is a G protein-coupled receptor that is activated by kynurenic acid and 2-acyl lysophosphatidic acids (e.g., 2-oleoyl lysophosphatidic acid).{24499,14771,24500} It is expressed predominantly on immune cells, the brain, and in the gastrointestinal tract.{14857,14771} GPR35 is overexpressed in gastric cancer cells.{13309} CID-2745687 is a reversible, competitive antagonist of GPR35, blocking activation by the synthetic agonist pamoic acid with a Ki value of 12.8 nM.{24501} It less potently blocks activation of GPR35 by zaprinast (Item No. 10010421) (IC50 = 160 nM).{24498} It shows ~57-fold selectivity for GPR35 over the related receptor GPR55 (IC50 = 9.08 µM).{24498}  

     

    Brand:
    Cayman
    SKU:12046 - 10 mg

    Available on backorder

  • GPR35 is a G protein-coupled receptor that is activated by kynurenic acid and 2-acyl lysophosphatidic acids (e.g., 2-oleoyl lysophosphatidic acid).{24499,14771,24500} It is expressed predominantly on immune cells, the brain, and in the gastrointestinal tract.{14857,14771} GPR35 is overexpressed in gastric cancer cells.{13309} CID-2745687 is a reversible, competitive antagonist of GPR35, blocking activation by the synthetic agonist pamoic acid with a Ki value of 12.8 nM.{24501} It less potently blocks activation of GPR35 by zaprinast (Item No. 10010421) (IC50 = 160 nM).{24498} It shows ~57-fold selectivity for GPR35 over the related receptor GPR55 (IC50 = 9.08 µM).{24498}  

     

    Brand:
    Cayman
    SKU:12046 - 25 mg

    Available on backorder

  • GPR35 is a G protein-coupled receptor that is activated by kynurenic acid and 2-acyl lysophosphatidic acids (e.g., 2-oleoyl lysophosphatidic acid).{24499,14771,24500} It is expressed predominantly on immune cells, the brain, and in the gastrointestinal tract.{14857,14771} GPR35 is overexpressed in gastric cancer cells.{13309} CID-2745687 is a reversible, competitive antagonist of GPR35, blocking activation by the synthetic agonist pamoic acid with a Ki value of 12.8 nM.{24501} It less potently blocks activation of GPR35 by zaprinast (Item No. 10010421) (IC50 = 160 nM).{24498} It shows ~57-fold selectivity for GPR35 over the related receptor GPR55 (IC50 = 9.08 µM).{24498}  

     

    Brand:
    Cayman
    SKU:12046 - 5 mg

    Available on backorder

  • GPR35 is a G protein-coupled receptor that is activated by kynurenic acid and 2-acyl lysophosphatidic acids (e.g., 2-oleoyl lysophosphatidic acid).{24499,14771,24500} It is expressed predominantly on immune cells, the brain, and in the gastrointestinal tract.{14857,14771} GPR35 is overexpressed in gastric cancer cells.{13309} CID-2745687 is a reversible, competitive antagonist of GPR35, blocking activation by the synthetic agonist pamoic acid with a Ki value of 12.8 nM.{24501} It less potently blocks activation of GPR35 by zaprinast (Item No. 10010421) (IC50 = 160 nM).{24498} It shows ~57-fold selectivity for GPR35 over the related receptor GPR55 (IC50 = 9.08 µM).{24498}  

     

    Brand:
    Cayman
    SKU:12046 - 50 mg

    Available on backorder

  • CID-2818500 is an inhibitor of protein arginine methyltransferase 1 (PRMT1; IC50 = 11 μM in a histone H4 methylation assay).{47652} It also inhibits histone H4 methylation by PRMT8, but not histone H3.1 methylation by CARM1 or Set7/9, when used at concentrations of 10 and 100 μM.  

     

    Brand:
    Cayman
    SKU:21919 -

    Out of stock

  • CID-2818500 is an inhibitor of protein arginine methyltransferase 1 (PRMT1; IC50 = 11 μM in a histone H4 methylation assay).{47652} It also inhibits histone H4 methylation by PRMT8, but not histone H3.1 methylation by CARM1 or Set7/9, when used at concentrations of 10 and 100 μM.  

     

    Brand:
    Cayman
    SKU:21919 -

    Out of stock

  • CID-2818500 is an inhibitor of protein arginine methyltransferase 1 (PRMT1; IC50 = 11 μM in a histone H4 methylation assay).{47652} It also inhibits histone H4 methylation by PRMT8, but not histone H3.1 methylation by CARM1 or Set7/9, when used at concentrations of 10 and 100 μM.  

     

    Brand:
    Cayman
    SKU:21919 -

    Out of stock

  • CID-2818500 is an inhibitor of protein arginine methyltransferase 1 (PRMT1; IC50 = 11 μM in a histone H4 methylation assay).{47652} It also inhibits histone H4 methylation by PRMT8, but not histone H3.1 methylation by CARM1 or Set7/9, when used at concentrations of 10 and 100 μM.  

     

    Brand:
    Cayman
    SKU:21919 -

    Out of stock

  • CID-2858522 is an 2-amino benzimidazole that inhibits activation of the NF-κB pathway induced by the PKC activator PMA with an IC50 value of 0.07 μM.{24527} It has been shown to inhibit IL-8 production induced by PKC activators in HEK293 cells (IC50 ≤ 0.1 μM), attenuate CD3/CD28 and PMA/ionomycin-induced production of IL-2 by Jurkat T cells (IC50 ≤ 5 μM), and prevent anti-IgM-stimulated proliferation of mouse B-lymphocytes (IC50 = ∼2 μM).{24527} CID-2858522 does not, however, inhibit the NF-κB pathway activated by TNF-α.{24527}  

     

    Brand:
    Cayman
    SKU:-
  • CID-2858522 is an 2-amino benzimidazole that inhibits activation of the NF-κB pathway induced by the PKC activator PMA with an IC50 value of 0.07 μM.{24527} It has been shown to inhibit IL-8 production induced by PKC activators in HEK293 cells (IC50 ≤ 0.1 μM), attenuate CD3/CD28 and PMA/ionomycin-induced production of IL-2 by Jurkat T cells (IC50 ≤ 5 μM), and prevent anti-IgM-stimulated proliferation of mouse B-lymphocytes (IC50 = ∼2 μM).{24527} CID-2858522 does not, however, inhibit the NF-κB pathway activated by TNF-α.{24527}  

     

    Brand:
    Cayman
    SKU:-
  • CID-2858522 is an 2-amino benzimidazole that inhibits activation of the NF-κB pathway induced by the PKC activator PMA with an IC50 value of 0.07 μM.{24527} It has been shown to inhibit IL-8 production induced by PKC activators in HEK293 cells (IC50 ≤ 0.1 μM), attenuate CD3/CD28 and PMA/ionomycin-induced production of IL-2 by Jurkat T cells (IC50 ≤ 5 μM), and prevent anti-IgM-stimulated proliferation of mouse B-lymphocytes (IC50 = ∼2 μM).{24527} CID-2858522 does not, however, inhibit the NF-κB pathway activated by TNF-α.{24527}  

     

    Brand:
    Cayman
    SKU:-
  • CID-2858522 is an 2-amino benzimidazole that inhibits activation of the NF-κB pathway induced by the PKC activator PMA with an IC50 value of 0.07 μM.{24527} It has been shown to inhibit IL-8 production induced by PKC activators in HEK293 cells (IC50 ≤ 0.1 μM), attenuate CD3/CD28 and PMA/ionomycin-induced production of IL-2 by Jurkat T cells (IC50 ≤ 5 μM), and prevent anti-IgM-stimulated proliferation of mouse B-lymphocytes (IC50 = ∼2 μM).{24527} CID-2858522 does not, however, inhibit the NF-κB pathway activated by TNF-α.{24527}  

     

    Brand:
    Cayman
    SKU:-
  • Brand:
    Cayman
    SKU:22967 - 1 mg

    Available on backorder

  • Brand:
    Cayman
    SKU:22967 - 10 mg

    Available on backorder

  • Brand:
    Cayman
    SKU:22967 - 25 mg

    Available on backorder

  • Brand:
    Cayman
    SKU:22967 - 5 mg

    Available on backorder

  • CID-5951923 is an inhibitor of the transcription factor Krüppel-like factor 5 (KLF5; IC50 = 2.3 μM).{35317} It decreases KLF5 expression in and reduces growth of DLD-1 colorectal adenocarcinoma cells in a concentration-dependent manner. CID-5951923 selectively inhibits proliferation of cancer cell lines that highly express KLF5, particularly colon adenocarcinomas, in the NCI-60 panel of cancer cell lines.  

     

    Brand:
    Cayman
    SKU:21649 -

    Out of stock

  • CID-5951923 is an inhibitor of the transcription factor Krüppel-like factor 5 (KLF5; IC50 = 2.3 μM).{35317} It decreases KLF5 expression in and reduces growth of DLD-1 colorectal adenocarcinoma cells in a concentration-dependent manner. CID-5951923 selectively inhibits proliferation of cancer cell lines that highly express KLF5, particularly colon adenocarcinomas, in the NCI-60 panel of cancer cell lines.  

     

    Brand:
    Cayman
    SKU:21649 -

    Out of stock

  • CID-5951923 is an inhibitor of the transcription factor Krüppel-like factor 5 (KLF5; IC50 = 2.3 μM).{35317} It decreases KLF5 expression in and reduces growth of DLD-1 colorectal adenocarcinoma cells in a concentration-dependent manner. CID-5951923 selectively inhibits proliferation of cancer cell lines that highly express KLF5, particularly colon adenocarcinomas, in the NCI-60 panel of cancer cell lines.  

     

    Brand:
    Cayman
    SKU:21649 -

    Out of stock

  • CID-5951923 is an inhibitor of the transcription factor Krüppel-like factor 5 (KLF5; IC50 = 2.3 μM).{35317} It decreases KLF5 expression in and reduces growth of DLD-1 colorectal adenocarcinoma cells in a concentration-dependent manner. CID-5951923 selectively inhibits proliferation of cancer cell lines that highly express KLF5, particularly colon adenocarcinomas, in the NCI-60 panel of cancer cell lines.  

     

    Brand:
    Cayman
    SKU:21649 -

    Out of stock

  • CID16020046 is a GPR55 inverse agonist that antagonizes GPR55 constitutive activity with an IC50 value of 15 μM.{29659} It inhibits GPR55-mediated ERK1/2 phosphorylation, LPI-induced Ca2+ signaling (IC50 = 0.21 μM in HEK-GPR55 cells), and GPR55-mediated transcription factor activation.{29659} It does not affect ERK1/2 phosphorylation or transcription factor activation in CB receptor expressing cells and demonstrates weak activity against a broad spectrum of other GPCRs, ion channels, kinases, and nuclear receptors.{29659} This compound has been shown to block GPR55-mediated endothelial wound healing and reverse LPI-inhibited platelet aggregation.{29659}  

     

    Brand:
    Cayman
    SKU:-
  • CID16020046 is a GPR55 inverse agonist that antagonizes GPR55 constitutive activity with an IC50 value of 15 μM.{29659} It inhibits GPR55-mediated ERK1/2 phosphorylation, LPI-induced Ca2+ signaling (IC50 = 0.21 μM in HEK-GPR55 cells), and GPR55-mediated transcription factor activation.{29659} It does not affect ERK1/2 phosphorylation or transcription factor activation in CB receptor expressing cells and demonstrates weak activity against a broad spectrum of other GPCRs, ion channels, kinases, and nuclear receptors.{29659} This compound has been shown to block GPR55-mediated endothelial wound healing and reverse LPI-inhibited platelet aggregation.{29659}  

     

    Brand:
    Cayman
    SKU:-
  • CID16020046 is a GPR55 inverse agonist that antagonizes GPR55 constitutive activity with an IC50 value of 15 μM.{29659} It inhibits GPR55-mediated ERK1/2 phosphorylation, LPI-induced Ca2+ signaling (IC50 = 0.21 μM in HEK-GPR55 cells), and GPR55-mediated transcription factor activation.{29659} It does not affect ERK1/2 phosphorylation or transcription factor activation in CB receptor expressing cells and demonstrates weak activity against a broad spectrum of other GPCRs, ion channels, kinases, and nuclear receptors.{29659} This compound has been shown to block GPR55-mediated endothelial wound healing and reverse LPI-inhibited platelet aggregation.{29659}  

     

    Brand:
    Cayman
    SKU:-
  • CID16020046 is a GPR55 inverse agonist that antagonizes GPR55 constitutive activity with an IC50 value of 15 μM.{29659} It inhibits GPR55-mediated ERK1/2 phosphorylation, LPI-induced Ca2+ signaling (IC50 = 0.21 μM in HEK-GPR55 cells), and GPR55-mediated transcription factor activation.{29659} It does not affect ERK1/2 phosphorylation or transcription factor activation in CB receptor expressing cells and demonstrates weak activity against a broad spectrum of other GPCRs, ion channels, kinases, and nuclear receptors.{29659} This compound has been shown to block GPR55-mediated endothelial wound healing and reverse LPI-inhibited platelet aggregation.{29659}  

     

    Brand:
    Cayman
    SKU:-
  • Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by diacylglycerol, commonly downstream of PKC signaling.{13335} The three human PKD isoforms target a variety of proteins to alter cell proliferation, survival, invasion, and protein transport. CID755673 is a small molecule inhibitor of PKD (IC50s = 182, 280, 227 nM for PKD1, 2, and 3, respectively) that exhibits higher selectivity for PKD over Akt, polo-like kinase 1, CDK activating kinase, CAMKII and three different PKC isoforms (IC50s range from 15 to > 50 µM).{25787} At 25 µM, CID755673 has been shown to inhibit prostate cancer cell proliferation, cell migration, and invasion.{25787}  

     

    Brand:
    Cayman
    SKU:-
  • Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by diacylglycerol, commonly downstream of PKC signaling.{13335} The three human PKD isoforms target a variety of proteins to alter cell proliferation, survival, invasion, and protein transport. CID755673 is a small molecule inhibitor of PKD (IC50s = 182, 280, 227 nM for PKD1, 2, and 3, respectively) that exhibits higher selectivity for PKD over Akt, polo-like kinase 1, CDK activating kinase, CAMKII and three different PKC isoforms (IC50s range from 15 to > 50 µM).{25787} At 25 µM, CID755673 has been shown to inhibit prostate cancer cell proliferation, cell migration, and invasion.{25787}  

     

    Brand:
    Cayman
    SKU:-
  • Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by diacylglycerol, commonly downstream of PKC signaling.{13335} The three human PKD isoforms target a variety of proteins to alter cell proliferation, survival, invasion, and protein transport. CID755673 is a small molecule inhibitor of PKD (IC50s = 182, 280, 227 nM for PKD1, 2, and 3, respectively) that exhibits higher selectivity for PKD over Akt, polo-like kinase 1, CDK activating kinase, CAMKII and three different PKC isoforms (IC50s range from 15 to > 50 µM).{25787} At 25 µM, CID755673 has been shown to inhibit prostate cancer cell proliferation, cell migration, and invasion.{25787}  

     

    Brand:
    Cayman
    SKU:-
  • Protein kinase D (PKD) is a serine/threonine protein kinase that is activated by diacylglycerol, commonly downstream of PKC signaling.{13335} The three human PKD isoforms target a variety of proteins to alter cell proliferation, survival, invasion, and protein transport. CID755673 is a small molecule inhibitor of PKD (IC50s = 182, 280, 227 nM for PKD1, 2, and 3, respectively) that exhibits higher selectivity for PKD over Akt, polo-like kinase 1, CDK activating kinase, CAMKII and three different PKC isoforms (IC50s range from 15 to > 50 µM).{25787} At 25 µM, CID755673 has been shown to inhibit prostate cancer cell proliferation, cell migration, and invasion.{25787}  

     

    Brand:
    Cayman
    SKU:-