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or refractory ischemia/repeat cardiac procedure) in patients with non-ST elevation acute coronary syndrome (NSTE-ACS)
InChiKey: UVSWWUWQVAQPJR-UHFFFAOYSA-N
The drug treatment led to tumor growth inhibition (TGI) of an EZH2 mutant KARPAS-422 DLBCL xenograft
and a Vss of 4
L-778123 hydrochloride Size:Contact [email protected] for quotation or refractory ischemia/repeat cardiac procedure)L 778123 hydrochloride is an inhibitor of FPTase and GGPTase I with IC50 of 2 nM and 98 nM in enzyme inhibition determination. IC50 value: 2 nM Target: FPTasein vitro: L 778123 can completely inhibit Ki Ras prenylation. L 778123 as a farnesyltransferase inhibitor can have a good cytotoxic activity as a classic anti cancer agent. in vivo: In the dog model, L 778123 inhibits HDJ2 prenylation and produces measurable, albeit slight (5%), levels of
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