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AT 406, 98%, 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
AT 406拮抗劑(訂貨以英文名稱為準(zhǔn))

  • 分子式: C32H43N5O4
  • 產(chǎn)品編號(hào): 1564197
  • 分子量: 562
  • CAS: 1071992-99-8
  • 純度: 98%
  • MDL: N/A
  • J&K