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InChiKey: FJAOGFGHTPYADT-SFHVURJKSA-N
Darbufelone is orally active and nonulcerogenic in animal models of inflammation and arthritis
Destruxin B significantly activates caspase-3 and reduces tumor cell proliferation through caspase-mediated apoptosis
Carbonic anhydrase inhibitors
PF-622 xy-2-phenethylchromone InChiKey: FJAOGFGHTPYADT-SFHVURJKSA-NPF 622 is a potent, time dependent, irreversible FAAH inhibitor . Fatty acid amide hydrolase (FAAH), belongs to a member of an unusual class of serine hydrolases, is an integral membrane enzyme involved in regulating the fatty acid amide family of lipid transmitters. Genetic or pharmacological inactivation of FAAH leads to elevated endogenous levels of fatty acid amides with analgesic, anti inflammatory, anxiolytic, and antidepressant phenotypes. The