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NADH-IN-1

目录号 : GC70952

NADH-IN-1具有抑制NADH:泛醌氧化还原酶活性,IC50值为27 μM。

NADH-IN-1 Chemical Structure

Cas No.:1432445-15-2

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥1,465.00
现货
5 mg
¥1,332.00
现货
10 mg
¥2,133.00
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25 mg
¥4,266.00
现货
50 mg
¥6,795.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

NADH-IN-1 has NADH:ubiquinone oxidoreductase inhibitory activity with an IC50 value of 27 μM. NADH-IN-1 can effectively stimulate glucose uptake in vitro. NADH-IN-1 is readily metabolised by the liver. NADH-IN-1 can be used for researching diabetes.

NADH-IN-1 (1 μM) exhibits a short half-life and fast intrinsic clearance indicating that it is readily metabolised by the liver in 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].

References:
[1]. Devine R, et al. Design, synthesis, and biological evaluation of aryl piperazines with potential as antidiabetic agents via the stimulation of glucose uptake and inhibition of NADH:ubiquinone oxidoreductase. Eur J Med Chem. 2020;202:112416.

Chemical Properties

Cas No. 1432445-15-2 SDF
分子式 C19H21F3N2OS 分子量 382.44
溶解度 DMSO : 200 mg/mL (522.96 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO) 储存条件 -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.6148 mL 13.0739 mL 26.1479 mL
5 mM 0.523 mL 2.6148 mL 5.2296 mL
10 mM 0.2615 mL 1.3074 mL 2.6148 mL
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