akash.verma@cenmed.com
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14015-25A natural diterpene that increases glutathione S-transferase expression and activity in vivo inhibits LPS-induced NO and PGE2 production (IC<sub>50</sub> = 54 and 23 &muM, respectively) in RAW macrophages blocks the proliferation of endothelial -
70690-10Ketorolac is a non-selective COX inhibitor. The IC<sub>50</sub> values for human recombinant COX-1 and -2 are 31.5 µM and 60.5 µM, respectively. -
16020-10PGF2&alpha tromethamine salt is a crystalline derivative of PGF2&alpha with increased water solubility. Its solubility in PBS is 25 mg/ml compared to 10 mg/ml for PGF2&alpha. -
18627-100A naturally-occurring tropane alkaloid that serves as an intermediate in the synthesis of a variety of bioactive alkaloids, many of which have potent neurological actions. -
14865-100Can be formed by the dimerization of two molecules of &alpha-trans-cinnamic acid significantly blocks inflammatory pain while having little effect on neurogenic pain, as indicated by the formalin test in mice. -
70690-5000Ketorolac is a non-selective COX inhibitor. The IC<sub>50</sub> values for human recombinant COX-1 and -2 are 31.5 µM and 60.5 µM, respectively. -
16220-55-trans PGF2&alpha tromethamine salt is a derivative of 5-trans PGF2&alpha with increased water solubility. Its solubility in PBS is 25 mg/ml compared to 10 mg/ml for 5-trans PGF2&alpha. -
16020-5PGF2&alpha tromethamine salt is a crystalline derivative of PGF2&alpha with increased water solubility. Its solubility in PBS is 25 mg/ml compared to 10 mg/ml for PGF2&alpha. -
18627-50A naturally-occurring tropane alkaloid that serves as an intermediate in the synthesis of a variety of bioactive alkaloids, many of which have potent neurological actions. -
14015-5A natural diterpene that increases glutathione S-transferase expression and activity in vivo inhibits LPS-induced NO and PGE2 production (IC<sub>50</sub> = 54 and 23 &muM, respectively) in RAW macrophages blocks the proliferation of endothelial -
18627-25A naturally-occurring tropane alkaloid that serves as an intermediate in the synthesis of a variety of bioactive alkaloids, many of which have potent neurological actions. -
16885-100A natural indole alkaloid with demonstrated beneficial effects in cancer, obesity, inflammation, and many other conditions an AhR antagonist (Ki = 28 nM), activator of TRPV1 (EC<sub>50</sub> = 45 nM), and inhibitor of signaling through NF-&kappaB.
