化学信息:
化学名 | 3-[1-[[4-(7-phenyl-3H-imidazo[4,5-g]quinoxalin-6-yl)phenyl]methyl]piperidin-4-yl]-1H-benzimidazol-2-one | |
简称 | AKT inhibitor VIII | |
别名 |
1,3-dihydro-PIQPBO, Akti-1/2, Imidazoquinoxaline |
|
中文名 | N/A | |
化学式 | C34H29N7O | |
分子量 | 551.64 | |
CAS号 | 612847-09-3 | |
纯度 | 98% | |
溶剂/溶解度 |
Water<1mg/ml; DMSO6mg/ml; Ethanol<1mg/ml |
|
溶液配制 | 5mg加入0.91ml DMSO,或者每5.52mg加入1ml DMSO,配制成10mM溶液。SF2784-10mM用DMSO配制。 |
生物信息:
产品描述 | Akt Inhibitor VIII is a cell-permeable quinoxaline compound that has been shown to potently, selectively, allosterically, and reversibly inhibit Akt1, Akt2, and Akt3 activity (IC50=58nM, 210nM, and 2.12μM; respectively). | ||||
信号通路 | PI3K/Akt/mTOR | ||||
靶点 | Akt1 | Akt2 | Akt3 | - | - |
IC50 | 58nM | 210nM | 2.12μM | - | - |
体外研究 | Akt Inhibitor VIII does not exhibit any inhibitory effect against pleckstrin homology (PH) domain-lacking Akts, AGC family kinases, PKA, PKC or SGK. Akt Inhibitor VIII prevails over Akt1/Akt2-mediated resistance to chemotherapeutics in tumor cells and has been shown to block basal and stimulated phosphorylation/activation of Akt1/Akt2 in cultured cells and in mice. | ||||
体内研究 | N/A | ||||
临床实验 | N/A | ||||
特征 | N/A |
相关实验数据(此数据来自于公开文献,碧云天并不保证其有效性):
酶活性检测实验 | |
方法 | N/A |
细胞实验 | |
细胞系 | N/A |
浓度 | N/A |
处理时间 | N/A |
方法 | N/A |
动物实验 | |
动物模型 | N/A |
配制 | N/A |
剂量 | N/A |
给药方式 | N/A |
产品编号 | 产品名称 | 包装 |
SF2784-10mM | AKT inhibitor VIII (Akt抑制剂) | 10mM×0.2ml |
SF2784-5mg | AKT inhibitor VIII (Akt抑制剂) | 5mg |
SF2784-25mg | AKT inhibitor VIII (Akt抑制剂) | 25mg |
— | 说明书 | 1份 |
保存条件:
-20℃保存,至少一年有效。5mg和25mg包装也可室温保存,至少6个月有效。如果溶于非DMSO溶剂,建议分装后-80℃保存,预计6个月内有效。