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Merck
CN

S8688

Sigma-Aldrich

SR 59230A

≥98% (HPLC), powder, β3-Adrenoceptor antagonist

别名:

3-(2-乙基苯氧基)-1-[[(1S)-1,2,3,4-四氢萘-1-基]氨基]-(2S)-2-丙醇 草酸盐

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关于此项目

经验公式(希尔记法):
C21H27NO2 · C2H2O4
化学文摘社编号:
分子量:
415.48
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
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产品名称

SR 59230A, ≥98% (HPLC), powder

质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white

溶解性

DMSO: >10 mg/mL
H2O: insoluble

创始人

Sanofi Aventis

SMILES字符串

OC(=O)C(O)=O.CCc1ccccc1OC[C@@H](O)CN[C@H]2CCCc3ccccc23

InChI

1S/C21H27NO2.C2H2O4/c1-2-16-8-4-6-13-21(16)24-15-18(23)14-22-20-12-7-10-17-9-3-5-11-19(17)20;3-1(4)2(5)6/h3-6,8-9,11,13,18,20,22-23H,2,7,10,12,14-15H2,1H3;(H,3,4)(H,5,6)/t18-,20-;/m0./s1

InChI key

XTBQNQMNFXNGLR-MKSBGGEFSA-N

基因信息

human ... ADRB3(155)

应用

SR 59230A用于& # 946;大鼠主动脉中的肾上腺素受体。3经测试,它被认为是一种改善心力衰竭大鼠模型心脏功能的潜在治疗剂。4

生化/生理作用

SR 59230A是一种& # 946;3-肾上腺素受体拮抗剂。它对& # 946;有很高的亲和力。3肾上腺素能受体出现在人体肠道中,影响人体结肠循环平滑肌的功能。1据报道SR 59230A抑制心脏钾通道2.1-2.3。2

特点和优势

该化合物在受体分类和信号转导手册中β-肾上腺素受体页面中进行了详细介绍。想要浏览手册的其他页面, 请单击此处
该化合物由Sanofi Aventis开发。要浏览其他药物开发化合物和批准的药物/候选药物列表,单击此处

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Understanding the mechanisms of immune tolerance is currently one of the most important challenges of scientific research. Pregnancy affects the immune system balance, leading the host to tolerate embryo alloantigens. Previous reports demonstrated that β-adrenergic receptor (β-AR) signaling promotes immune
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European journal of pharmacology, 723, 62-66 (2013-11-28)
The effect of two novel β3-adrenoceptor (β3-AR) agonists SP-1f and SP-1h on human colon circular smooth muscle contractility and β3-AR mRNA expression have been determined. β3-AR is ascertained co-participates to the control of the gut motility. Isometric tension on human
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Stimulation of the heart beta 3-adrenoceptor (AR) may result in a negative inotropic effect. Being up-regulated, beta 3-AR plays a more important role in the regulation of cardiac function during heart failure. However, the effect of chronic blocking of beta
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Biochemical and biophysical research communications, 424(2), 315-320 (2012-07-04)
Kir2.x channels form the molecular basis of cardiac I(K1) current and play a major role in cardiac electrophysiology. However, there is a substantial lack of selective Kir2 antagonists. We found the β(3)-adrenoceptor antagonist SR59230A to be an inhibitor of Kir2.x

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