跳转至内容
Merck
CN

I160

3-(1H-Imidazol-4-yl)propyl di(p-fluorophenyl)methyl ether hydrochloride

powder

登录 查看组织和合同定价。

选择尺寸


关于此项目

经验公式(希尔记法):
C19H18F2N2O · HCl
分子量:
364.82
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

InChI

1S/C19H18F2N2O.ClH/c20-16-7-3-14(4-8-16)19(15-5-9-17(21)10-6-15)24-11-1-2-18-12-22-13-23-18;/h3-10,12-13,19H,1-2,11H2,(H,22,23);1H

SMILES string

Cl.Fc1ccc(cc1)C(OCCCc2c[nH]cn2)c3ccc(F)cc3

InChI key

LCHACRBDLUKTTM-UHFFFAOYSA-N

form

powder

color

pale gray

solubility

H2O: >4 mg/mL, methanol: 50 mg/mL, DMSO: 7 mg/mL

Gene Information

human ... HRH3(11255)

Biochem/physiol Actions

H3 histamine receptor antagonist.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Novel histamine H3-receptor antagonists with benzyl ether structure or related moieties: Synthesis and structure-activity relationships.
Huls, A., et al.
Archives of Pharmacal Research, 329, 379-379 (1996)
Diphenylmethyl ethers: Synthesis and histamine H3-receptor antagonist in vitro and in vivo activity.
Huls, A., et al.
Bioorganic & Medicinal Chemistry Letters, 6, 2013-2018 (1996)
H Stark et al.
Die Pharmazie, 52(7), 495-500 (1997-07-01)
This study was performed in order to develop new leads for antagonists of the histamine H3-receptor subtype. omega-(1 H-Imidazol-4-yl)alkyl derivatives with ester, ketone or alcohol functionality in the side chain were synthesized and tested concerning their H3-receptor antagonist activity on

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持