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BMS 599626 714971-09-2

简要描述:BMS 599626 714971-09-2
AC480 (BMS-599626) is a selective and efficacious inhibitor of HER1 and HER2 with IC50 of 20 nM and 30 nM, ~8-fold less potent to HER4, >100-fold to VEGFR2, c-Kit, Lck, MET etc

  • 产品型号:abs47028108
  • 厂商性质:生产厂家
  • 更新时间:2026-01-19
  • 访  问  量:593

详细介绍

品牌absinCAS714971-09-2
分子式C27H27FN8O3纯度>98%
分子量530.55货号abs47028108
规格5mg供货周期现货
主要用途is a selective and efficacious inhibitor应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

BMS 599626  714971-09-2

产品描述
描述

AC480 (BMS-599626) is a selective and efficacious inhibitor of HER1 and HER2 with IC50 of 20 nM and 30 nM, ~8-fold less potent to HER4, >100-fold to VEGFR2, c-Kit, Lck, MET etc. Phase 1.

纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
AC480;BMS-599626
可溶性/溶解性
Ethanol :16 mg/mL (30.2 mM)

DMSO :104 mg/mL (196 mM)
生物活性
靶点
HER1 ,HER2,HER4
In vitro(体外研究)
BMS-599626 also inhibits the related receptor HER4, but with reduced potency with IC50 of 190 nM. BMS-599626 is identified as an ATP-competitive inhibitor for HER1 and as an ATP-noncompetitive inhibitor for HER2 with Ki of 2 nM and 5 nM, respectively. BMS-599626 inhibits the proliferation of tumor cells expressing high levels of HER1 and/or HER2, including Sal2, BT474, N87, KPL-4, HCC202, HCC1954, HCC1419, AU565, ZR-75-30, MDA-MB-175, GEO, and PC9 cells with IC50 of 0.24 μM, 0.31 μM, 0.45 μM, 0.38μM, 0.94 μM, 0.34 μM, 0.75 μM, 0.63 μM, 0.51 μM, 0.84 μM, 0.90 μM and 0.34 μM, respectively. While the proliferation of the ovarian tumor cell line A2780 and MRC5 fibroblasts, neither of which expresses HER1 or HER2, are not inhibited significant by BMS-599626. A recent study shows that BMS-599626 significantly enhances the radiosensitivity of HN-5 cells expressing both EGFR and Her2 cell, by promoting cycle redistribution and inhibiting DNA repair.
In vivo(体内研究)
In vivo, oral administration of BMS-599626 results in a dose-dependent inhibition of Sal2 tumor growth at doses ranging from 60 mg/kg to 240 mg/kg, yielding a potent antitumor activity in a human breast tumor KPL-4 xenograft at its maximum tolerated dose of 180 mg/kg, and also has similar antitumor activity in other HER2 amplified xenograft models, as well as other HER1-overexpressing xenograft models.
参考文献
参考文献
1. Wong TW, et al. Clin Y Res, 2006, 12(20 Pt 1), 6186-6193.
研究领域
研究领域
CancerGrowth factorsEGF
CancerOncoproteins/suppressorsOncoproteinsGrowth factor receptors
CancerSignal transductionProtein phosphorylationTyrosine kinasesReceptor tyrosine kinases
CancerTumor biomarkersReceptors
Cell CycleCell differentiation
MicrobiologyOrganismVirusDNA VirusssRNA positive strand virusSARS Coronavirus
NeuroscienceDevelopment
NeuroscienceProcesses
Signal TransductionGrowth Factors/HormonesEGF
Signal TransductionProtein PhosphorylationTyrosine KinasesReceptor Tyrosine Kinases
Drug DiscoverySmall Molecule DrugLead Compound Discovery
BMS 599626  714971-09-2温馨提示:本产品仅作科研实验使用,不支持临床等研究

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