搜索结果

Search Results for " strand transfer "

抑制剂 & 化合物

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T6420	BMS-707035 N-[(4-氟苯基)甲基1,6-二氢-5-羟基-1-甲基-6-氧代-2-(四氢-1,1-二氧-2H-1,2-噻嗪-2-基)-4-嘧啶甲酰胺	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	BMS707035是一种 HIV-1 整合酶抑制剂，IC50为15 nM。
T6098	Cabotegravir GSK744,GSK-1265744,卡博特韦,S/GSK1265744	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Cabotegravir (S/GSK1265744) 是一种HIV 整合酶抑制剂，可研究艾滋病。它抑制OAT1 和OAT3，IC50值为 0.81 和0.41 μM。
T2332	Elvitegravir 埃替格韦,GS-9137,EVG,D06677,JTK-303	HIV Protease	Microbiology/Virology; Proteases/Proteasome
	Elvitegravir (JTK-303) 是一种人类免疫缺陷病毒整合酶链转移抑制剂，作用于 HIV-1IIIB、HIV-2EHO 和 HIV-2ROD，IC50分别为 0.7 nM、2.8 nM 和 1.4 nM。
T11568	HIV-1 integrase inhibitor 4	Others	Others
	HIV-1 integrase inhibitor 4 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 3.7 nM).
T11567	HIV-1 integrase inhibitor 3	Others	Others
	HIV-1 integrase inhibitor 3 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 2.7 nM).
T73524	XZ426
	XZ426 是一种有效的整合酶链转移抑制剂，具有抗HIV 活性。
T70881	Dolutegravir RR Isomer
	Dolutegravir RR Isomer is an isomer of Dolutegravir -- a second generation HIV-1 integrase strand transfer inhibitor. Dolutegravir has been shown to potently inhibit HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector.
T68364	GS-9160
	GS-9160 is a novel and potent inhibitor of human immunodeficiency virus type 1 (HIV-1) integrase (IN) that specifically targets the process of strand transfer. It is an authentic inhibitor of HIV-1 integration, since treatment of infected cells results in an elevation of two-long terminal repeat circles and a decrease of integration junctions.
T71009	Dolutegravir SR Isomer
	Dolutegravir SR Isomer is an isomeric derivative of Dolutegravir -- a second generation HIV-1 integrase strand transfer inhibitor. Dolutegravir has been shown to potently inhibit HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector.
T36794	Dolutegravir O-β-D-Glucuronide
	Dolutegravir O-β-D-glucuronide is a metabolite of the HIV integrase inhibitor dolutegravir .1It is formed from dolutegravir primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A1in vivobut is also metabolized by UGT1A9 in human liver and kidney microsomes and UGT1A3 in human intestinal microsomes.2,1 1.Liu, S.N., Lu, J.B., Watson, C.J.W., et al.Mechanistic assessment of extrahepatic contributions to glucuronidation of integrase strand transfer inhibitorsDrug Metab. Dispos.47(5)535-544...

化合物

BMS-707035

Cat.No: T6420

Synonym: N-[(4-氟苯基)甲基1,6-二氢-5-羟基-1-甲基-6-氧代-2-(四氢-1,1-二氧-2H-1,2-噻嗪-2-基)-4-嘧啶甲酰胺

Target: HIV Protease

Cabotegravir

Cat.No: T6098

Synonym: GSK744,GSK-1265744,卡博特韦,S/GSK1265744

Target: HIV Protease

Elvitegravir

Cat.No: T2332

Synonym: 埃替格韦,GS-9137,EVG,D06677,JTK-303

Target: HIV Protease

HIV-1 integrase inhibitor 4

Cat.No: T11568

Synonym:

Target: Others

HIV-1 integrase inhibitor 3

Dolutegravir RR Isomer

Dolutegravir SR Isomer

Cat.No: T71009

Synonym:

Target:

Dolutegravir O-β-D-Glucuronide

Cat.No: T36794

Synonym:

Target:

Cat. No.	Product Name	Target	Signaling Pathways
T36000	3-Hydroxyterphenyllin
	3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,3,4 It has a 96% scavenging effect on 2,2-diphenyl-1-picrylhydrazyl radicals when used at a concentration of 100 μg/ml.2 3-Hydroxyterphenyllin inhibits the growth of HeLa cervical, A549 lung, and HepG2 liver cancer cells (IC50s = 23, 36, and 32 μM, respectively), as well as methi...

天然产物

3-Hydroxyterphenyllin

Cat.No: T36000

Synonym:

Target:

* 搜索：		* 机关/企业：
* 邮箱：		* 电话：
备注：
验证码：

搜索结果

抑制剂 & 化合物

天然产物

提交您的定制咨询

化合物

天然产物