| 溶解性 | DMSO ≥60mg/mL Water <1.2mg/mL Ethanol ≥1.8mg/mL |
| 存贮条件 | 储存温度-20°C |
| 应用 | A selective large conductance calcium activated potassium channel activator |
| 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。 |
| 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. |
| 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. |
| 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 |
BIIB021,HSP90抑制剂
BIIB021 （订货以英文为准）
编号：B127837
CAS号：848695-25-0
分子式：C14H15CLN6O
分子量：318.77
| 产品名称 | BIIB021 |
| 中文名称 | BIIB021,HSP90抑制剂 |
| CAS号 | 848695-25-0 |
| 分子式（M.F.） | C14H15CLN6O |
| 分子量（M.W.） | 318.77 |
| 储存条件 | -20°C储存 |
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