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• 產(chǎn)品描述： Xevinapant (AT-406) is a potent and orally bioavailable Smac mimetic and an antagonist of IAPs, and it binds to XIAP, cIAP1, and cIAP2 proteins with Ki of 66.4, 1.9, and 5.1 nM, respectively.

• 靶點： cIAP1:1.9 nM (Ki);cIAP2:5.1 nM (Ki);XIAP:66.4 nM (Ki);IAP

• 體內(nèi)研究：
  Xevinapant (AT-406) is very effective in inhibition of tumor growth in the MDA-MB-231 xenograft model, and has minimal toxicity to animals.Xevinapant is evaluated for its pharmacokinetic (PK) properties in mice, rats, non-human primates and dogs.

• 參考文獻：
  1. Cai Q, Sun H, Peng Y, et al. A potent and orally active antagonist (SM-406/AT-406) of multiple inhibitor of apoptosis proteins (IAPs) in clinical development for cancer treatment. J Med Chem. 2011;54(8):2714-2726.

• 溶解性： DMSO  :  100  mg/mL  (178.03  mM;  Need  ultrasonic)

• 保存條件： -20℃

• 配置溶液濃度參考：
  

  	1mg	5mg	10mg
  1 mM	1.78 ml	8.901 ml	17.803 ml
  5 mM	0.356 ml	1.78 ml	3.561 ml
  10 mM	0.178 ml	0.89 ml	1.78 ml
  50 mM	0.036 ml	0.178 ml	0.356 ml

• 注意：部分產(chǎn)品我司僅能提供部分信息，我司不保證所提供信息的權(quán)威性，僅供客戶參考交流研究之用。

輸入產(chǎn)品批號：

本計算器可幫助您計算出特定溶液中溶質(zhì)的質(zhì)量、溶液濃度和體積之間的關(guān)系，公式為：

質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

• pg ng μg mg g kg =
  fM pM nM μM mM M *
  nL μL mL L *