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名称: BIIB021英文名称: BIIB021≥98%产品编号 B127837
CAS号: 848695-25-0分子式 C14H15ClN6O分子量318.77
溶解性 | DMSO ≥60mg/mL Water |
存贮条件 | 储存温度-20°C |
产品介绍 | BIIB021(CNF2024)是口服活性的HSP90抑制剂,Ki和EC50分别为1.7 nM和38 nM。 |
别名 | BIIB-021; BIIB 021; 6-氯-9-((4-甲氧基-3,5-二甲基-2-吡啶基)甲基)-9H-嘌呤-2-胺;;CNF2024; ;CNF 2024;CNF-2024;6-chloro-9-((4-methoxy-3,5-dimethyl-2-pyridinyl)methyl)-9h-purin-2-amine;1,3-Dihydro-1-[2-hydroxy-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-2H-benzimidazol-2-one |
生化机理 | Oral administration of BIIB021 leads to tumor growth inhibition in many tumor xenograft models including N87, BT474, CWR22, U87, SKOV3 and Panc-1. BIIB021 effectively inhibits growth of L540cy tumor at a dose of 120 mg/kg. BIIB021 significantly enhances antitumor growth effect of radiation in JHU12 xenograft. |
备注 | BIIB021 is an orally available, fully synthetic small-molecule inhibitor of HSP90 with Ki and EC50 of 1.7 nM and 38 nM, respectively. |
应用 | A selective large conductance calcium activated potassium channel activator |
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