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SL910102 Sale

目录号 : GC32591

SL910102是一种非肽类的血管紧张素AT1受体拮抗剂。

SL910102 Chemical Structure

Cas No.:144756-71-8

规格 价格 库存 购买数量
1mg
¥13,405.00
现货
5mg
¥21,456.00
现货
10mg
¥34,335.00
现货

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Sample solution is provided at 25 µL, 10mM.

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实验参考方法

Kinase experiment:

For saturation as well as displacement studies, rat lung homogenate is incubated in either Hepes-buffer or blank human or rat plasma yielding 50 μg protein per well in a total assay volume of 300 μL. To ensure equilibrium conditions (see binding kinetics), the samples are maintained for 60 min at 25°C under continuous rotation. All experiments are carried out in duplicate, and the results are confirmed with n=3-5 replicates over the following days[1].

References:

[1]. Soldner A, et al. A radioreceptor assay for the analysis of AT1-receptor antagonists. Correlation with complementary LC data reveals a potential contribution of active metabolites. J Pharm Biomed Anal. 1998 May;17(1):111-24.

产品描述

SL910102 is a nonpeptide angiotensin AT1 receptor antagonist.

SL910102 (SL 91.0102-90 DL) is a unlabelled nonpeptide AT1-antagonist, which is tested for its ability to compete with [125J](Sar1-Ile8)-angiotensin II for specific AT1-receptor sites in rat lung homogenate[1].

[1]. Soldner A, et al. A radioreceptor assay for the analysis of AT1-receptor antagonists. Correlation with complementary LC data reveals a potential contribution of active metabolites. J Pharm Biomed Anal. 1998 May;17(1):111-24.

Chemical Properties

Cas No. 144756-71-8 SDF
Canonical SMILES O=C1N=C(CCC2=CC=CC=C2)NC(CCCC)=C1CC3=CC=C(C4=CC=CC=C4C5=NN=NN5)C=C3
分子式 C30H30N6O 分子量 490.6
溶解度 Soluble in DMSO 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.0383 mL 10.1916 mL 20.3832 mL
5 mM 0.4077 mL 2.0383 mL 4.0766 mL
10 mM 0.2038 mL 1.0192 mL 2.0383 mL
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