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Merck
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文件

I2279

Sigma-Aldrich

IMID-4F hydrochloride

solid, solubility: >9 mg/mL in H2O, soluble

别名:

2-[N-(2,6-dichlorophenyl)-N-(4-fluorobenzyl)amino]-2-imidazoline hydrochloride

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About This Item

经验公式（希尔记法）:
C16H14Cl2FN3 ·HCl
CAS号:
1049740-09-1
分子量:
374.67
MDL號碼:
MFCD03452939
分類程式碼代碼:
12352202
PubChem物質ID:
24278489
NACRES:
NA.77

化驗

≥98%

形狀

solid

顏色

white

溶解度

H2O: soluble >9 mg/mL

SMILES 字串

Cl[H].Fc1cccc(CN(C2=NCCN2)c3c(Cl)cccc3Cl)c1

InChI

1S/C16H14Cl2FN3.ClH/c17-13-5-2-6-14(18)15(13)22(16-20-7-8-21-16)10-11-3-1-4-12(19)9-11;/h1-6,9H,7-8,10H2,(H,20,21);1H

InChI 密鑰

TWVCONNNZSKLLX-UHFFFAOYSA-N

生化／生理作用

Novel imidazoline-based K(ATP) channel blocker.

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

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G A McPherson et al.
British journal of pharmacology, 128(8), 1636-1642 (1999-12-10)
1. The functional and electrophysiological effects of IMID-4F (2-[N-(2, 6-dichlorophenyl)-N-(4-flurorobenzyl)amino]imidazoline), a fluoro-benzyl derivative of clonidine, on vascular K(ATP) channels were investigated. In pig coronary artery, IMID-4F inhibited the vasorelaxation response to the K(ATP) channel opener levcromakalim with a pK(B) value
K Bell et al.
Naunyn-Schmiedeberg's archives of pharmacology, 362(2), 145-151 (2000-08-29)
In this study the activity of a number of novel imidazoline-based compounds (IMID series) was assessed by functional and binding studies to determine their actions at K(ATP) channels. The novel compounds, which we synthesised, were methoxy-, methyl-, butyl- and fluorophenyl

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