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CP-640186
本产品不向个人销售，仅用作科学研究，不用于任何人体实验及非科研性质的动物实验。
CP-640186图片
CAS NO:591778-68-6
包装:1mg
市场价:1239元

产品介绍
CP-640186 是一种具有口服活性和细胞渗透性的乙酰辅酶 A 羧化酶 (ACC) 抑制剂，对大鼠肝脏 ACC1 和大鼠骨骼肌 ACC2 的 IC50 分别为 53 nM 和 61 nM。
Cas No.591778-68-6
化学名(R)-anthracen-9-yl(3-(morpholine-4-carbonyl)-[1,4'-bipiperidin]-1'-yl)methanone
Canonical SMILESO=C(N1CCOCC1)[C@]2([H])CCCN(C3CCN(C(C4=C5C=CC=CC5=CC6=CC=CC=C64)=O)CC3)C2
分子式C30H35N3O3
分子量485.62
溶解度≥ 19.95mg/mL in DMSO
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

CP-640186 is a potent and cell-permeable Acetyl-CoA carboxylase (ACC) inhibitor with IC50s of 53 nM and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2 respectively.

References:
[1]. Harwood HJ Jr, et al. Isozyme-nonselective N-substituted bipiperidylcarboxamide acetyl-CoA carboxylase inhibitors reduce tissue malonyl-CoA concentrations, inhibit fatty acid synthesis, and increase fatty acid oxidation in cultured cells and in experimental animals. J Biol Chem. 2003 Sep 26;278(39):37099-111.
[2]. Yamashita T, et al. Design, synthesis, and structure-activity relationships of spirolactones bearing 2-ureidobenzothiophene as acetyl-CoA carboxylases inhibitors. Bioorg Med Chem Lett. 2011 Nov 1;21(21):6314-8.