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(+)-Etomoxir is an inhibitor of carnitine palmitoyltransferase 1 (CPT1) and a prodrug form of (+)-etomoxir (Cay-11969). It is an ethyl ester that is cleaved by intracellular esterases to release the active inhibitor of CPT1. (+)-Etomoxir decreases palmitate (Cay-10010279) oxidation and increases glucose oxidation in isolated rat myocytes when used in a concentration-dependent manner. It reduces mitochondrial oxygen consumption rates and increases free fatty acid levels in LoVo colorectal cancer cells when used at a concentration of 40 µM. (+)-Etomoxir (25 mg/kg per day for five days) inhibits kidney tubule necrosis and dilation and reduces blood urea nitrogen (BUN) and serum creatinine levels in a mouse model of acute kidney damage induced by ischemia and reperfusion.. Solulibility: DMSO: Soluble: =10 mg/ml: Ethanol: Sparingly soluble: 1-10 mg/ml.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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