分子式:C18H16N2O,分子量:276.33,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,SC66 is a novel AKT inhibitor, IC50 values of approximately 0.75 μg/ml at 72 hours in HepG2, HA22T/VGH and PLC/PRF/5 cells.
货号 | 规格 | 数量 | 价格 |
---|---|---|---|
Q-0022294 | 100mg |
1
|
询价 |
Q-0022294 | 250mg |
1
|
询价 |
Q-0022294 | 500mg |
1
|
询价 |
Q-0022294 | 1g |
1
|
询价 |
Q-0022294 | 5g |
1
|
询价 |
参数信息 | |
---|---|
外观状态: | 固体或粉末 |
质量指标: | 95%+ |
溶解条件: | 有机溶剂/水 |
CAS号: | N/A |
分子量: | N/A |
储存条件: | -20℃避光保存 |
储存时间: | 1年 |
运输条件: | 室温2周 |
生产厂家: | 西安齐岳生物科技有限公司 |
-
常用名 METHYL 2-((TRIMETHYLSILYL)ETHYNYL)BENZOATE 英文名 METHYL 2-((TRIMETHYLSILYL)ETHYNYL)BENZOATE CAS号 107793-07-7
-
常用名 Methyl 2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinoline]-5'-carboxylate hydrochloride 英文名 Methyl 2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-isoquinoline]-5'-carboxylate hydrochloride CAS号 1203684-69-8
-
分子式:C22H21N3O2,分子量:359.42,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,YM-90709 is a novel antagonist which inhibits the binding of interleukin-5 to interleukin-5 receptor.
-
分子式:C19H17N3O2Scl2,分子量:422.32,溶解性: (R.T.: 25℃): DMSO,KM11060 is a novel corrector of the F508del-CFTR trafficking defect.