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CUDC-427

    
≥99%

CUDC-427

源叶(MedMol)
S83365 一键复制产品信息
1446182-94-0
C29H36N6O4S
564.6989
CUDC-427; GDC-0917; (S)-1-((S)-2-cyclohexyl-2-((S)-2-(methylamino)propanamido)acetyl)-N-(2-(oxazol-2-yl)-4-phenylthiazol-5-yl)pyrrolidine-2-carboxamide; (S)-1-[(S)-2-cyclohexyl-2-((S)-2-methylamino-pr
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S83365-5mg
≥99%

¥710.00

货期:3-5天 - - - -
S83365-10mg
≥99%

¥1120.00

货期:3-5天 - - - -
S83365-50mg
≥99%

¥2910.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: CUDC-427 is a potent second-generation pan-selective IAP antagonist, used for treatment of various cancers.
靶点: IAP
体外研究: GDC-0917 (0.1 nM-10 μM) induces reduction of cIAP1 levels in PBMCs in a concentration-dependent manner showing greater than 80% inhibition at concentrations greater than 0.1 µM (56.5 ng/mL)
体内研究: GDC-0917 (0.08-16.3 mg/kg) exhibits antitumor activity in a dose dependent manner in the MDA-MB-231-X1.1 Breast Cancer Xenograft, and GDC-0917 is well tolerated, with all dose groups experiencing a <11% decrease in mean body weight. GDC-0917 has low to moderate clearance in the mouse (12.0 mL/min/kg), rat (27.0 mL/min/kg), and dog (15.3 mL/min/kg), and high clearance in the monkey (67.6 mL/min/kg). Oral bioavailability is lowest in monkeys compared with other species
参考文献: 1. Wong H, et al. Learning and confirming with preclinical studies: modeling and simulation in the discovery of GDC-0917, an inhibitor of apoptosis proteins antagonist. Drug Metab Dispos. 2013 Dec;41(12):2104-13.
溶解性: soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.771 ml 8.854 ml 17.709 ml
5 mM 0.354 ml 1.771 ml 3.542 ml
10 mM 0.177 ml 0.885 ml 1.771 ml
50 mM 0.035 ml 0.177 ml 0.354 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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