纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,B-Raf IN 1 is a highlt potent and selective B-Raf inhibitor with IC50 of 24 nM
货号 | 规格 | 数量 | 价格 |
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Q-0019230 | 100mg |
1
|
询价 |
Q-0019230 | 250mg |
1
|
询价 |
Q-0019230 | 500mg |
1
|
询价 |
Q-0019230 | 1g |
1
|
询价 |
Q-0019230 | 5g |
1
|
询价 |
参数信息 | |
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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 |
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常用名 METHYL 2-((TRIMETHYLSILYL)ETHYNYL)BENZOATE 英文名 METHYL 2-((TRIMETHYLSILYL)ETHYNYL)BENZOATE CAS号 107793-07-7
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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
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分子式:C16H13N2Oscl,分子量:316.80,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,LH846 is a selective inhibitor of CK1δ (IC50 values are 290 nM, 1.3 uM and 2.5 uM for CK1δ, ε and α)
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分子式:C28H34N2O.2[HCl],分子量:487.50,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,GBR 12935 dihydrochloride inhibits DAT (dopamine transporter) (Ki = 21.5 nM) and SLC6A2 (norepinephrine transporter) (Ki = 225 nM).