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Nevanimibe
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。
Nevanimibe图片
CAS NO:133825-80-6
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品名称
PD-132301
ATR-101
产品介绍
Nevanimibe (PD-132301) 是一种口服有效的,选择性酰基辅酶 A:胆固醇 O-酰基转移酶 1 (ACAT1) 抑制剂,EC50为 9 nM。Nevanimibe 抑制 ACAT2,EC50为 368 nM。Nevanimibe 诱导细胞凋亡 (apoptosis),并具有抗肾上腺皮质癌的潜力。
生物活性

Nevanimibe (PD-132301) is an orally active and selective acyl-coenzyme A:cholesterol O-acyltransferase 1 (ACAT1) inhibitor with anEC50of 9 nM. Nevanimibe inhibitsACAT2with an EC50of 368 nM. Nevanimibe induces cellapoptosisand has the potential for adrenocorticalcancer[1].

IC50& Target

ACAT1

9 nM (EC50)

ACAT2

368 nM (EC50)

体外研究
(In Vitro)

Coincubation of Nevanimibe (PD-132301; ATR101; 3 nM-30 μM) and Cholesterol markedly increases toxicity in a dose-dependent manner, where 3 nM Nevanimibe in the presence of 60 μg/mL Cholesterol reduces survival by 60% after 24 hours. All doses of Nevanimibe (3 nM-30 μM) induces cytoxicity in the presence of Cholesterol, whereas treatment with Cholesterol in the absence of Nevanimibe has no effect on cell viability[1].

Cell Cytotoxicity Assay[1]

Cell Line:The H295R and HAC clone 15 (HAC15) human ACC cell lines
Concentration:3 nM-30 μM
Incubation Time:24 hours
Result:3 nM-3 μM exhibited no toxicity, whereas 30 μM treatment reduced survival by approximately 40% within 24 hours.
Clinical Trial
分子量

421.62

Formula

C27H39N3O

CAS 号

133825-80-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.