分子式:C25H27N5,分子量:397.51,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,AT-56 is am orally active inhibitor of lipocalin-type prostaglandin D synthase (L-PGDS) (Ki = 75 μM, IC50 = 95 μM)
货号 | 规格 | 数量 | 价格 |
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Q-0019147 | 100mg |
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询价 |
Q-0019147 | 250mg |
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询价 |
Q-0019147 | 500mg |
1
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询价 |
Q-0019147 | 1g |
1
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询价 |
Q-0019147 | 5g |
1
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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:C19H19N3OF4,分子量:381.36726,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,HPGDS inhibitor 1 is a novel and selective Hematopoietic Prostaglandin D Synthase (HPGDS) inhibitor with an IC50 Value of 0.7 nM. IC50 Value: 0.7 nM.
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分子式:C16H20N8O,分子量:340.383,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO