Cayman Amoxapine; Purity- Greater Than Or Equal To 95%; Size- 1 G

BMS 214662 is a potent inhibitor of farnesyltransferase (FTase; IC₅₀ = 1.3 nM). It is selective for FTase over geranylgeranyl transferase (GGTase; IC₅₀ = 1,900 nM). It inhibits the growth of MEK2, A2780, and PC3 cancer cells expressing wild-type Ras (IC₅₀s = 2.5, 0.04, and 0.15 μM, respectively), as well as HCT116, MIP, RC-165, and MIA PaCa-2 cells expressing mutant K-Ras (IC₅₀s = 0.06, 0.3, 0.3, and 0.12 μM, respectively). BMS 214662 induces apoptosis in HCT116 cells in a concentration-dependent manner. In vivo, BMS 214662 (600 mg/kg) is curative in an HCT116 mouse xenograft model. It also reduces tumor growth in Calu-1, HT-29, EJ-1, and MIA PaCa-2 mouse xenograft models.

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