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InChiKey: CILIXQOJUNDIDU-ASQIGDHWSA-N
It is rapidly absorbed after oral administration
A66 is a potent inhibitor of the wild-type and oncogenic forms of p110α but not other class-I PI3K isoforms
Smiles: CC(C)C[C@H](NC(=O)OCC1=CC=CC=C1)C(=O)N[C@@H](CCC(=O)OC)C(=O)N[C@@H](CC1=CN=CN1)C(=O)N[C@@H](CC(=O)OC)C(=O)CF
) potentiates the toxicity produced by yohimbine in mice
CP-547632 3654 InChiKey: CILIXQOJUNDIDU-ASQIGDHWSA-NCP 547632 is an orally active, ATP competitive and potent VEGFR 2 and FGF kinases inhibitor with IC50s of 11 nM and 9 nM, respectively. CP 547632 is selective for VEGFR2 and bFGF over EGFR, PDGFR, and related tyrosine kinases (TKs). CP 547632 has antitumor efficacy. Product information CAS Number: 252003 65 9 Molecular Weight: 532. 40 Formula: C20H24BrF2N5O3S Chemical Name: 3 [(4 bromo 2,6 difluorophenyl)methoxy] 5 ({[4 (pyrrolidin 1