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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.

产品文档

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产品描述

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.

Chemical Properties

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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动物体内配方计算器 (澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
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