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HZ-1157
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
HZ-1157图片
CAS NO:1009734-33-1
包装与价格:
包装价格(元)
5mg询价
25mg询价

HZ-1157 抑制 HCV NS3/4A 蛋白酶,IC50 为 1.0 μmol/L。
Cas No.1009734-33-1
别名5-叔丁氧基-2,4-二氨基喹唑啉
化学名5-(tert-butoxy)quinazoline-2,4-diamine
Canonical SMILESNC1=NC(N)=NC2=CC=CC(OC(C)(C)C)=C21
分子式C12H16N4O
分子量232.28
溶解度≥ 11.6mg/mL in DMSO
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

HZ-1157 is a potent hepatitis C virus (HCV) inhibitor toward HCV NS3/4A protease with IC50 value of 1.0 μmol/L [1].

The NS3 protease of HCV is a prime target for the development of anti-HCV agents because it cleaves the viral polyprotein and liberates NS3, NS4A, NS4B, NS5A, and NS5B, allowing them to function normally in viral RNA replication, and it deactivates many host proteins involved in innate immunity to foster a favorable cellular environment for HCV replication. The NS3 protease is most active when complexed with its cofactor NS4A [1].

In vitro: Huh7.5.1 cell line stably transfected with HCV NS3/4A protease reporter was established to investigate the anti-HCV mechanism of HZ-1157 (0.001~1 μmol/L). The results showed that HZ-1157 exhibited inhibitory effect on the HCV NS3/4A protease with IC50 value of 1.0 μmol/L. HZ-1157 was further tested against an infectious HCV virus (J399EM) which can infect and replicate in Huh7.5.1 cells in vitro. The results showed that HZ-1157 effectively inhibited J399EM virus replication in Huh7.5.1 cells with IC50 value of 0.82 μmol/L [1].

Reference:
[1].  Yu Y, Jing J, Tong X, et al. Discovering novel anti-HCV compounds with inhibitory activities toward HCV NS3/4A protease[J]. Acta Pharmacologica Sinica, 2014, 35(8): 1074.

 
 
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