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Pactimibe sulfate
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。
Pactimibe sulfate图片
规格:98%
分子量:465.65
包装与价格:
包装价格(元)
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Pactimibe sulfate (CS-505) 是一种 ACAT1/2 双重抑制剂,对于 ACAT1 的 IC50 值为 4.9 µM,对于 ACAT2 的 IC50 值为 3.0 µM。Pactimibe sulfate (CS-505) 抑制 ACAT,其 IC50 值在肝细胞中是 2.0 µM,在巨噬细胞中是 2.7 µM,在 THP-1 细胞中是 4.7 µM。Pactimibe sulfate (CS-505) 非竞争性抑制 oleoyl-CoA,Ki 是5.6 µM。此外,Pactimibe sulfate (CS-505) 明显抑制胆固醇酯的形成,IC50 是6.7 µM。Pactimibe sulfate (CS-505) 具有抗动脉粥样硬化的潜力,可降低血浆胆固醇的活性。
货号:ajcx32646
CAS:608510-47-0
分子式:C25H40N2O3.1/2H2O4S
分子量:465.65
溶解度:DMSO : 120 mg/mL (257.70 mM)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Pactimibe sulfate (CS-505) is a dual ACAT1/2 inhibitor with IC50s of 4.9 µM and 3.0 µM, respectively. Pactimibe sulfate (CS-505) inhibits ACAT with IC50s of 2.0 µM, 2.7 µM, 4.7 µM in the liver, macrophages and THP-1 cells, respectively[1]. Pactimibe sulfate (CS-505) noncompetitively inhibits oleoyl-CoA with a Ki value of 5.6 µM. Moreover, Pactimibe sulfate (CS-505) obviously inhibits cholesteryl ester formation with an IC50 of 6.7 µM. Pactimibe sulfate (CS-505) possesses anti-atherosclerotic potential with lowering plasma cholesterol activity[2].

Pactimibe sulfate (CS-505) induces moderate ACAT inhibition in monocyte-derived macrophages, leading to the suppression of foam cell formation[2].

Pactimibe sulfate (CS-505; 60 and 200 mg/kg/day; oral gavage; twice a day; 12 weeks) induces an inhibition for ACAT-1 and ACAT-2, causing a reduction of plasma cholesterol but no influence on macrophage- or collagen-positive areas[3].

参考文献:
[1]. Naoki Terasaka, et al. ACAT inhibitor pactimibe sulfate (CS-505) reduces and stabilizes atherosclerotic lesions by cholesterol-lowering and direct effects in apolipoprotein E-deficient mice. Atherosclerosis. 2007 Feb;190(2):239-47.
[2]. Ken Kitayama, et al. Importance of acyl-coenzyme A:cholesterol acyltransferase 1/2 dual inhibition for anti-atherosclerotic potency of pactimibe. Eur J Pharmacol. 2006 Jul 1;540(1-3):121-30.
[3]. Yasunobu Yoshinaka, et al. A selective ACAT-1 inhibitor, K-604, stimulates collagen production in cultured smooth muscle cells and alters plaque phenotype in apolipoprotein E-knockout mice. Atherosclerosis. 2010 Nov;213(1):85-91.

 
 
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