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Merck
CN

I127

Sigma-Aldrich

ICI 118,551 盐酸盐

≥98% (HPLC), powder, β2 inverse agonist

别名:

(2R,3R)-rel-3-异丙胺-1-(7-甲基吲哚-4-氧基)-丁-2-醇 盐酸盐

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关于此项目

经验公式(希尔记法):
C17H27NO2 · HCl
化学文摘社编号:
分子量:
313.86
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

ICI 118,551 盐酸盐, ≥98% (HPLC), powder

质量水平

方案

≥98% (HPLC)

表单

powder

储存条件

desiccated

颜色

white

溶解性

H2O: >10 mg/mL

SMILES字符串

Cl.CC(C)N[C@@H](C)[C@@H](O)COc1ccc(C)c2CCCc12

InChI

1S/C17H27NO2.ClH/c1-11(2)18-13(4)16(19)10-20-17-9-8-12(3)14-6-5-7-15(14)17;/h8-9,11,13,16,18-19H,5-7,10H2,1-4H3;1H/t13-,16-;/m0./s1

InChI key

KBXMBGWSOLBOQM-LINSIKMZSA-N

基因信息

human ... ADRB2(154)

应用

ICI 118,551 盐酸已用于:
  • 在各种实验中阻挡β-肾上腺素信号
  • 通过内源性T淋巴细胞单胺氧化酶抑制降解
  • 测定异丙肾上腺素上调基因转录所需的特定受体压型

生化/生理作用

ICI 118,551 盐酸盐是一种高选择性 β2-肾上腺素受体拮抗剂。
ICI 118,551已用于治疗与焦虑相关的血管舒缩性偏头痛和体细胞疾病。

特点和优势

该化合物在受体分类和信号转导手册中β-肾上腺素能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

免责声明

吸湿

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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访问文档库

beta-Adrenergic-stimulated macrophages: comprehensive localization in the M1-M2 spectrum
Lamkin DM, et al.
Brain, behavior, and immunity, 57(, 338-346 (2016)
Analysis of ICI 118551, a new beta2 blocking drug, and related compounds by RP-HPLC?DAD
Quaglia MG, et al.
Journal of Pharmaceutical and Biomedical Analysis, 10(10-12), 1081-1084 (1992)
Hongliang Li et al.
The Journal of biological chemistry, 288(42), 30734-30741 (2013-09-18)
Functional autoantibodies to the autonomic receptors are increasingly recognized in the pathophysiology of cardiovascular diseases. To date, no human activating monoclonal autoantibodies to these receptors have been available. In this study, we describe for the first time a β2-adrenergic receptor
R M Booze et al.
The Journal of pharmacology and experimental therapeutics, 249(3), 911-920 (1989-06-01)
The localization and number of beta adrenergic receptors were directly compared in the brains of rats and guinea pigs. The time course of association and saturability of [125I]cyanopindolol (CYP) binding to slide-mounted tissue sections was similar in rats (Kd =
M R Bristow et al.
Molecular pharmacology, 35(3), 295-303 (1989-03-01)
Prenalterol (beta 1-agonist), denopamine (beta 1-agonist), and zinterol (beta 2-agonist) were partial agonists of adenylate cyclase (AC) stimulation in human ventricular myocardium obtained from nonfailing chambers whose beta 1/beta 2 receptor subtype ratio was approximately 80/20. At a concentration less

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