CP-640186 MedChemExpress (MCE)

Product Name	CP-640186
Synonyms	CS-1316 CP-640186 CP 640186 (R)-Anthracen-9-yl(3-(morpholine-4-carbonyl)-[1,4'-bipiperidin]-1'-yl)methanone (R)-ANTHRACEN-9-YL(3-(MORPHOLINE-4-CARBONYL)-1,4'-BIPIPERIDIN-1'-YL)METHANONE.HCL Synonyms CS-1316 CP-640186 CP 640186 (R)-Anthracen-9-yl(3-(morpholine-4-carbonyl)-[1,4'-bipiperidin]-1'-yl)methanone (R)-ANTHRACEN-9-YL(3-(MORPHOLINE-4-CARBONYL)-1,4'-BIPIPERIDIN-1'-YL)METHANONE.HCL (Anthracen-9-yl)[(3R)-3-[(morpholin-4-yl)carbonyl][1,4']bipiperidinyl-1'-yl]methanone [(3R)-1-[1-(anthracene-9-carbonyl)piperidin-4-yl]piperidin-3-yl]-morpholin-4-ylmethanone (R)-anthracen-9-yl(3-(morpholine-4-carbonyl)-[1,4'-bipiperidin]-1'-yl)metha none CP640186 CP 640186 (R)-ANTHRACEN-9-YL(3-(MORPHOLINE-4-CARBONYL)-1,4'-BIPIPERIDIN-1'-YL)METHANONE.HCL
CAS	591778-68-6
EINECS
Chemical Formula	C30H35N3O3
Molecular Weight	485.62
inchi
Package	10 mM * 1 mL;5 mg;10 mg;25 mg;50 mg
Price	Email to quote
Descriptions	CP-640186 CP-640186 MedChemExpress (MCE) HY-15259 591778-68-6 99.72% Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month Room temperature in continental US Descriptions CP-640186 CP-640186 MedChemExpress (MCE) HY-15259 591778-68-6 99.72% Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month Room temperature in continental US may vary elsewhere. CP-640186 is an orally active 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. Acetyl-CoA carboxylase (ACC) is a key enzyme of fatty acid metabolism that enables the synthesis of malonyl-CoA. CP-640186 can also stimulate muscle fatty acid oxidation. CP-640186 (20 µM 48 h) treatment can inhibit H460 cell growth[3]. CP-640186 (0.1 nM-100 µM 2 h) treatment increases fatty acid metabolism in a concentration-dependent manner in C2C12 cells and muscle strips[1]. CP-640186 (0.62-1.8 µM 2 h) treatment inhibits fatty acid synthesis and TG synthesis in HepG2 cells[1]. CP-640186 (oral gavage 4.6-21 mg/kg once) demonstrates acute efficacy[1]. CP-640186 (intravenous injection and oral gavage Intravenous dose, 5 mg/kg oral dose, 10 mg/kg once) shows lowe drug exposure in the rat than the ob/ob mouse at equal doses[1]. CP-640186 (oral gavage 100 mg/kg once) treatment shows a complete shift from carbohydrate utilization to fatty acid utilization as a source of energy at high exposure level[1]. IC50: 53 nM (rat liver ACC1) and 61 nM (rat skeletal muscle ACC2)[1] Cellular Effect Cell Line Type Value Description 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 experiment [Content Brief] [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. [Content Brief] [3]. Daniel Hess, et al. Inhibition of stearoylCoA desaturase activity blocks cell cycle progression and induces programmed cell death in lung cancer cells. PLoS One. 2010 Jun 30 5(6):e11394. [Content Brief]
Last Update	2025-04-01 14:45:47

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