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LCAHA (Synonyms: LCA hydroxyamide) 纯度: 98.05%
LCAHA (LCA hydroxyamide) 是一种脱泛素酶 USP2a 抑制剂,在 Ub-AMC 分析和 Di-Ub 分析中, IC50 分别为 9.7 μM 和 3.7 μM。LCAHA 通过抑制去泛素酶 USP2a 破坏细胞周期蛋白 D1 稳定性并诱导 G0/G1 期阻滞。
LCAHA Chemical Structure
CAS No. : 117094-40-3
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥4400 | In-stock | |
5 mg | ¥4000 | In-stock | |
10 mg | ¥8000 | In-stock | |
25 mg | ¥16500 | In-stock | |
50 mg | ¥25500 | In-stock | |
100 mg | ¥38000 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
* Please select Quantity before adding items.
LCAHA 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 |
LCAHA (LCA hydroxyamide) is a deubiquitinase USP2a inhibitor with IC50s of 9.7 μM and 3.7μM in Ub-AMC Assay and Di-Ub Assay, respectively. LCAHA destabilizes Cyclin D1 and induces G0/G1 arrest by inhibiting deubiquitinase USP2a[1]. |
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体外研究 (In Vitro) |
LCAHA inhibits HCT116wt and HCT116 p53-/- colon cancer cells viability with GI50s of 0.87±0.09 and 0.96±0.29μM, respectively, and the LD50s of 27.8±3.9 and 26.5±0.1μM, respectively[1]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability Assay[1]
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分子量 |
391.59 |
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Formula |
C24H41NO3 |
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CAS 号 |
117094-40-3 |
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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 : 45 mg/mL (114.92 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。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
*以上所有助溶剂都可在 Shanghai Jinpan Biotech Co Ltd 网站选购。
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参考文献 |
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