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Sephin1 was orally dosed to MPZmutant mice or SOD1mutant mice at 1 mg/Kg twice a day
donor substrates of farnesylation and geranylgeranylation during the post-translational modification of small GTPase signalling proteins
Chemical Name: 4-fluoro-5-{[(2S)-2-methyl-1
Molecular Weight: 371
BTK Inhibitor
Pravastatin Sodium Catalog No.:M9367-10 Sephin1 was orally dosed toPravastatin Sodium is an antilipemic fungal metabolite isolated from cultures of Nocardia autotrophica. It acts as a competitive inhibitor of HMG CoA reductase Pravastatin competitively inhibits hepatic hydroxymethyl glutaryl coenzyme A reductase, the enzyme which catalyzes the conversion of HMG CoA to mevalonate, a key step in cholesterol synthesis. This agent lowers plasma cholesterol and lipoprotein levels, and modulates immune responses by
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