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1163-36-6

中文名稱 1-[(4-氯苯基)甲基]-2-(吡咯烷-1-基甲基)苯并咪唑鹽酸鹽
英文名稱 Clemizole hydrochloride
CAS 1163-36-6
EINECS 編號 214-605-4
分子式 C19H21Cl2N3
MDL 編號 MFCD00051435
分子量 362.3
MOL 文件 1163-36-6.mol
更新日期 2024/10/25 11:12:36
1163-36-6 結(jié)構(gòu)式 1163-36-6 結(jié)構(gòu)式

基本信息

中文別名
1-[(4-氯苯基)甲基]-2-(吡咯烷-1-基甲基)苯并咪唑鹽酸鹽
鹽酸氯咪唑
英文別名
1-[(4-Chlorophenyl)methyl]-2-(pyrrolidin-1-ylmethyl)benzoimidazole hydrochloride
1-P-CHLOROBENZYL-2-[1-PYRROLIDINYL]-METHYLBENZIMIDAZOLE HYDROCHLORIDE
CLEMIZOLE HCL
CLEMIZOLE HYDROCHLORIDE
LABOTEST-BB LT00453174
1-(p-chlorobenzil)-2-pirrolidil-metil-benzimidazolocloridato
1-(p-chlorobenzyl)-2-(1-pyrrolidinylmethyl)-benzimidazolmonohydrochloride
1-p-chlorobenzyl-pyrrolidyl-methylene-benzimidazolehydrochloride
allercur
allercurehydrochloride
p48
1-(4-Chlorophenyl)methyl)-2-(1-pyrrolidinylmethyl)-(1H)-benzimidazoleHCl
1-(P-CHLOROBENZYL)-2-(1-PYRROLIDINYLMETHYL)-BENZIMIDAZOL
所屬類別
生物化工:激動劑抑制劑

物理化學(xué)性質(zhì)

熔點239-241°
儲存條件Inert atmosphere,2-8°C
溶解度在水中的溶解度為性2mg/mL,澄清(加熱)
形態(tài)粉末
顏色白色至米色
水溶解性16.84mg/L at 25℃
Merck13,2368
InChIKeyDNFMJYXRIMLMBZ-UHFFFAOYSA-N
LogP1.99
CAS 數(shù)據(jù)庫1163-36-6(CAS DataBase Reference)

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302
防范說明P301+P312+P330
危險品標(biāo)志Xn
危險類別碼R22
安全說明S36
WGK Germany3
RTECS號DD6730000
海關(guān)編碼2933.99.8290

應(yīng)用領(lǐng)域

用途一
用作氯咪唑青霉素等藥物的中間體
1-[(4-氯苯基)甲基]-2-(吡咯烷-1-基甲基)苯并咪唑鹽酸鹽價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/08/19HY-30234A1-[(4-氯苯基)甲基]-2-(吡咯烷-1-基甲基)苯并咪唑鹽酸鹽
Clemizole hydrochloride
1163-36-65mg500元
2024/08/19HY-30234A1-[(4-氯苯基)甲基]-2-(吡咯烷-1-基甲基)苯并咪唑鹽酸鹽
Clemizole hydrochloride
1163-36-610mM * 1mLin DMSO550元
2024/08/19HY-30234A1-[(4-氯苯基)甲基]-2-(吡咯烷-1-基甲基)苯并咪唑鹽酸鹽
Clemizole hydrochloride
1163-36-610mg800元

常見問題列表

生物活性
Clemizole hydrochloride 是一種 H1 組胺受體 (H1 histamine receptor) 拮抗劑,抑制 HCV 復(fù)制。
靶點

IC50: 24 nM (NS4B)
H1 histamine receptor

體外研究

Clemizole hydrochloride is found to inhibit HCV RNA replication in cell culture that is mediated by its suppression of NS4B’s RNA binding, with little toxicity for the host cell. The EC 50 of Clemizole on the W55R mutant J6/JFH RNA is ~18 μM (2.25 times the EC 50 of the wild-type RNA). Clemizole is a novel inhibitor of TRPC5 channels. Clemizole efficiently blocks TRPC5 currents and Ca 2+ entry in the low micromolar range (IC 50 =1.0-1.3 μM). Clemizole exhibits a six-fold selectivity for TRPC5 over TRPC4β (IC 50 =6.4 μM), the closest structural relative of TRPC5, and an almost 10-fold selectivity over TRPC3 (IC 50 =9.1 μM) and TRPC6 (IC 50 =11.3 μM). Clemizole hydrochloride as a novel blocker of TRPC5 with a half-maximal inhibitory concentration of 1.1 μM. The concentration-response curves confirmed a concentration-dependent block of TRPC5 by Clemizole and revealed an apparent IC 50 of 1.1±0.04 μM.

體內(nèi)研究

Clemizole hydrochloride has an unexpectedly short plasma half-life (measured at 0.15 hours); it is very rapidly biotransformed into a glucuronide (M14) and a dealkylated metabolite (M12) and into a variety of lesser metabolites in C57BL/6J mice.

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