分子式:C18H25N7O,分子量:355.43,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,RO9021 是一种可口服的,ATP 竞争性的 SYK **剂,IC50 值为 5.6 nM。
货号 | 规格 | 数量 | 价格 |
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Q-0023702 | 100mg |
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Q-0023702 | 250mg |
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Q-0023702 | 500mg |
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Q-0023702 | 1g |
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Q-0023702 | 5g |
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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:C23H25N6O2F3, 分子量:474.4788, 纯度: > 98%, 溶解性: (R.T.: 25℃): DMSO, PF-03814735 is a novel, potent and reversible inhibitor of Aurora A/B with IC50of 0.8 nM/5 nM, is less potent to Flt3, FAK, TrkA, and minimally active to Met and FGFR1. Phase 1.
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分子式:C19H16N2O5, 分子量:352.34074, 纯度: > 98%, 溶解性: (R.T.: 25℃): DMSO, IOX2 is a potent inhibitor of HIF-1α prolyl hydroxylase-2 (PHD2) with IC50 of 21 nM in a cell-free assay, >100-fold selectivity over JMJD2A, JMJD2C, JMJD2E, JMJD3, or the 2OG oxygenase FIH.