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Merck

C5423

Sigma-Aldrich

克仑特罗 盐酸盐

≥95% (TLC), powder, β2-adrenoceptor agonist

别名:

4-氨基-& # 945;-(叔丁基氨基甲基)-3,5-二氯苄醇 盐酸盐

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About This Item

经验公式(希尔记法):
C12H18Cl2N2O · HCl
CAS号:
分子量:
313.65
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

产品名称

克仑特罗 盐酸盐, ≥95%

方案

≥95%

表单

powder

drug control

Home Office Schedule 4.2

储存温度

2-8°C

SMILES字符串

Cl.CC(C)(C)NCC(O)c1cc(Cl)c(N)c(Cl)c1

InChI

1S/C12H18Cl2N2O.ClH/c1-12(2,3)16-6-10(17)7-4-8(13)11(15)9(14)5-7;/h4-5,10,16-17H,6,15H2,1-3H3;1H

InChI key

OPXKTCUYRHXSBK-UHFFFAOYSA-N

基因信息

human ... ADRB2(154)

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应用

盐酸克伦特罗已被用作:
  • 来自鸡骨骼肌的 β-肾上腺素能受体(β -AR)的激动剂,以诱导大鼠
  • 的咬肌、二腹肌和颞肌中的肥大效应。
  • 作为串联质谱(MS-MS)中的参照β-激动剂标准

生化/生理作用

盐酸克伦特罗是一种& # 946;2-肾上腺素受体激动剂和支气管扩张剂。它能有效改善哮喘患者的呼气峰流速(PEFR)。克伦特罗也是一种提高性能的药物,因为它刺激中枢神经系统并改善氧转运。克伦特罗在扩张型心肌病患者中引发心脏保护功能。

象形图

Health hazard

警示用语:

Danger

危险声明

危险分类

Carc. 2 - Repr. 1B

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A trial of clenbuterol in bronchial asthma.
Anderson G and Wilkins E
Thorax, 32(6), 717-719 (1977)
C A Izeboud et al.
Inflammation research : official journal of the European Histamine Research Society ... [et al.], 48(9), 497-502 (1999-10-16)
To investigate the suppressive effects of the beta-agonist clenbuterol on the release of TNF-alpha and IL-6 in a lipopolysaccharide (LPS)-model of inflammation, both in vitro and in vivo. Human U-937 cell line (monocyte-derived macrophages), and male Wistar rats (200-250 g).
Jelka Pleadin et al.
Meat science, 86(3), 733-737 (2010-07-30)
The aim of this study was to determine the level of clenbuterol residues in muscle tissue of pigs after repeat administration in a growth-promoting dose. An anabolic dose of clenbuterol (20 μg/kg body mass per day) was administered orally to
Effects of clenbuterol, a beta2-adrenergic agonist, on sizes of masseter, temporalis, digastric, and tongue muscles
Ishikawa C, et al.
The Open Dentistry Journal, 3, 191-191 (2009)
H M Zuurmond et al.
Molecular pharmacology, 56(5), 909-916 (1999-10-26)
Previously, we demonstrated the involvement of Asn293 in helix VI of the human beta(2)-adrenergic receptor in stereoselective agonist recognition and activation. In the present study, we have further explored the role of this residue by synthesizing derivatives of isoproterenol and

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