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NADH-IN-1
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。
NADH-IN-1图片
CAS NO:1432445-15-2

NADH-IN-1 对NADH: 泛醌氧化还原酶 (NADH:ubiquinone oxidoreductase)具有抑制活性,IC50为 27 μM。NADH-IN-1 在体外能有效刺激葡萄糖摄取。NADH-IN-1易被肝脏代谢。可用于糖尿病的研究。
生物活性

NADH-IN-1 hasNADH:ubiquinone oxidoreductaseinhibitory activity with anIC50value of 27 μM. NADH-IN-1 can effectively stimulate glucose uptakein vitro. NADH-IN-1 is readily metabolised by the liver. NADH-IN-1 can be used for researching diabetes[1].

IC50& Target

IC50: 27 μM (NADH:ubiquinone oxidoreductase)[1]

体内研究
(In Vivo)

NADH-IN-1 (1 μM) exhibits a short half-life and fast intrinsic clearance indicating that it is readily metabolised by the liverin vivo; shows no adverse effects on primary rat hepatocytes, and does not inhibit the hERG channel[1].
NADH-IN-1 (10 mg/kg; IV or PO; single dosage) produces no observable toxic effects at 10 mg/kg by IV or PO; exhibits a short half-life and high plasma clearance; exhibits high mouse and human serum protein binding, as well as moderate bioavailability[1].

Animal Model:Male C57BL/6 mice[1]
Dosage:10 mg/kg
Administration:IV or PO; single dosage (Pharmacokinetics Analysis)
Result:Produced no observable toxic effects at 10 mg/kg by IV or PO; exhibited a short half-life of 0.45 h and high plasma clearance; exhibited high mouse and human serum protein binding, as well as moderate bioavailability (21.4%).
分子量

382.44

Formula

C19H21F3N2OS

CAS 号

1432445-15-2

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.

 
 
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