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现货供应对照品CP-547632
产品型号:C13504
英文简称:
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产品详情
Chemical Name: 3-(4-Bromo-2,6-difluorobenzyloxy)-5-[3-[4-(1-pyrrolidinyl)butyl]ureido]isothiazole-4-carboxamide
分子式:C20H24BrF2N5O3S
分子量:532.40
纯度:>99%
CAS:252003-65-9
Biological Activity:
CP-547,632 is as
a potent inhibitor of the VEGFR-2 and basic fibroblast growth
factor (FGF) kinases (IC
50
= 11 and 9 nM, respectively). It
is selective relative to epidermal growth factor receptor, platelet-derived
growth factor ß, and other related TKs. It also inhibits
VEGF-stimulated autophosphorylation of VEGFR-2 in a whole cell
assay with an IC
50
value of 6 nM. After oral administration
of CP-547,632 to mice bearing NIH3T3/H-ras tumors, VEGFR-2 phosphorylation
in tumors was inhibited in a dose-dependent fashion (EC
50
=
590 ng/ml). These plasma concentrations correlated well with
the observed concentrations of the compound necessary to inhibit
VEGF-induced corneal angiogenesis in BALB/c mice. A sponge angiogenesis
assay was used to directly compare the inhibitory activities
of CP-547,632 against FGF receptor 2 or VEGFR-2; this compound
potently inhibits both basic FGF and VEGF-induced angiogenesis
in vivo
. The antitumor efficacy of this agent was evaluated
after once daily p.o. administration to athymic mice bearing
human xenografts and resulted in as much as 85% tumor growth
inhibition. CP-547,632 is a well-tolerated, orally-bioavailable
inhibitor presently under clinical investigation for the treatment
of human malignancies.
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