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HP661

目录号 : GC91057

一种线粒体复合物I抑制剂。

HP661 Chemical Structure

规格 价格 库存 购买数量
1 mg
¥1,572.00
现货
5 mg
¥6,676.00
现货

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Sample solution is provided at 25 µL, 10mM.

Description

HP661 is an inhibitor of mitochondrial complex I, also known as NADH dedrogenase.1 It is selective for complex I, inhibiting it by 77.6%, over complex III, which it inhibits by 28.1%, and complexes II and IV, which it does not inhibit, at 1 µM. HP661 selectively reduces viability of the human lung cancer cells H460, NCI H441, and trametinib-resistant A549 cells (IC50s = 10.6, 29.7, and 15.1 nM, respectively), which all have high levels of oxidative phosphorylation, over NCI H358 human lung cancer cells (IC50 = >10,000 nM), which have low levels of oxidative phosphorylation, and non-cancerous human pancreatic normal epithelial (HPNE) and MRC-5 human fetal lung fibroblast cells (IC50s = >10,000 nM for both). HP661 reduces tumor volume in an H460 mouse xenograft model when administered at a dose of 30 mg/kg twice per day and has an additive effect on trametinib-induced reduction of tumor growth.

化学性质

Cas No. SDF
分子式 C31H29F6N7O3 分子量 661.6
溶解度 Chloroform: Soluble,Methanol: Soluble 储存条件 Store at -20°C
General tips 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。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 1.5115 mL 7.5574 mL 15.1149 mL
5 mM 0.3023 mL 1.5115 mL 3.023 mL
10 mM 0.1511 mL 0.7557 mL 1.5115 mL
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