上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。
STD1T 纯度: 98.77%
STD1T 是一种脱泛素酶 USP2a 抑制剂,在 Ub-AMC 分析中, IC50 为 3.3 μM。

STD1T Chemical Structure
CAS No. : 893075-58-6
规格 | 价格 | 是否有货 | 数量 |
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5 mg | ¥4800 | In-stock | |
10 mg | ¥8000 | In-stock | |
50 mg | 询价 | ||
100 mg | 询价 |
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STD1T 相关产品
•相关化合物库:
- Bioactive Compound Library Plus
- Cell Cycle/DNA Damage Compound Library
- Anti-Cancer Compound Library
- Anti-Aging Compound Library
- Ubiquitination Compound Library
生物活性 |
STD1T is a deubiquitinase USP2a inhibitor with an IC50 of 3.3 μM in Ub-AMC Assay[1]. |
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体外研究 (In Vitro) |
STD1T inhibits USP2a enzymatic activity in a concentration dependent manner. STD1T shows selective inhibition of USP2a vs. USP7 at the concentrations of 10 µM and 2000 µM, respectively[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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分子量 |
417.50 |
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Formula |
C19H19N3O4S2 |
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CAS 号 |
893075-58-6 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 62.5 mg/mL (149.70 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
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参考文献 |
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