K-Ras-PDEδ-IN-1 Size:Contact [email protected] for quotation [H]/N=C(/N)\SCCC1C=CC(CCS/C(/N)=N/[H])=CC=1

[H]/N=C(/N)\SCCC1C=CC(CCS/C(/N)=N/[H])=CC=1

Smiles: CCOC(=O)NC1=CC=C(NCC2C=CC(F)=CC=2)N=C1N

and orally active prostaglandin D2 receptor CRTH2 antagonist

24 and 48 h) arrests cells at the G1 phase of the cell cycle

GPVI-stimulated platelet aggregation is inhibited in GS-9876-treated monkeys without a concomitant increase in bleeding time (BT)

K-Ras-PDEδ-IN-1 Size:Contact [email protected] for quotation [H]/N=C(/N)\SCCC1C=CC(CCS/C(/N)=N/[H])=CC=1K Ras PDE IN 1 is a novel and potent competitive K Ras PDE inhibitor. K Ras PDE IN 1 binds to the farnesyl binding pocket of PDE with a low nanomolar Kd of 8 nM. Product information CAS Number: 1841464 21 8 Molecular Weight: 447. 50 Formula: C25H26FN5O2 Chemical Name: N [2 (4 fluorophenyl)ethyl] 4 [4 methyl 2 (4 methylphenyl) 7 oxo 2H,6H,7H pyrazolo[3,4 d]pyridazin 6 yl]butanamide Smiles: