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HCV Protease

HCV Protease

NS2-3 protease (of hepatitis C virus, HCV) is an enzyme responsible for proteolytic cleavage between NS2 and NS3, which are non-structural proteins that form part of the HCV virus particle. NS3 protease of hepatitis C virus, on the other hand, is responsible for the cleavage of non-structural protein downstream. Both of these proteases are directly involved in HCV genome replication, that is, during the viral life-cycle that leads to virus multiplication in the host that has been infected by the virus.
TargetMol
1 2 3 4 5 6 7
Cat. No. Product Name CAS No. Purity Chemical Structure
TN1033 Sennidin A
番泻苷元A
641-12-3 100%
TargetMol Chemical Structure Sennidin A
Sennidin A 是从狭叶番泻分离得到的一种天然产物,能够抑制 HCV NS3 解旋酶,其 IC50值为0.8 μM。它诱导 Akt 和葡萄糖转运蛋白4的磷酸化,刺激葡萄糖掺入。
TN1138 γ-Fagarine
γ-崖椒碱
524-15-2
TargetMol Chemical Structure γ-Fagarine
gamma-Fagarine possesses moderate levels of anti-HCV activities with IC50 values being 20.4 ± 0.4 ug/ml, respectively. It has sister chromatid exchanges (SCEs)-i...
TN1034 Sennidin B
番泻苷元B
517-44-2
TargetMol Chemical Structure Sennidin B
Sennidin B 是从Cassia angustifolia 分离得到的Sennidin A 异构体,它刺激葡萄糖掺入,诱导Akt 和葡萄糖转运蛋白4 的磷酸化。
T5539 GS-443902
瑞德西韦代谢物
1355149-45-9
TargetMol Chemical Structure GS-443902
Remdesivir triphosphate 是一种有效的病毒 RNA 依赖的 RNA 聚合酶抑制剂,对RSVRdRp 和 HCVRdRp 的IC50分别为 1.1 µM 和 5 µM。它是 Remdesivir 的活性三磷酸代谢物。
TN3809 Dehydrojuncusol
化合物 TN3809
117824-04-1 98%
TargetMol Chemical Structure Dehydrojuncusol
Dehydrojuncusol, a new inhibitor of hepatitis C virus RNA replication, it inhibits infection of different HCV genotypes by targeting the NS5A protein and is acti...
T12966 Sofosbuvir impurity K
索非布韦杂质 K
1496552-51-2 98%
TargetMol Chemical Structure Sofosbuvir impurity K
Sofosbuvir impurity K is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
T12969 Sofosbuvir impurity N
索非布韦杂质 N
1394157-34-6 98%
TargetMol Chemical Structure Sofosbuvir impurity N
Sofosbuvir impurity N is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
T12033 Micrococcin P1
微球菌素 P1
67401-56-3 98%
TargetMol Chemical Structure Micrococcin P1
Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor(EC50 range of 0.1-0.5 μM)
T12965 Sofosbuvir impurity J
索非布韦杂质 J
1334513-10-8 98%
TargetMol Chemical Structure Sofosbuvir impurity J
Sofosbuvir impurity J is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
T12963 Sofosbuvir impurity H
化合物 T12963
T12963 98%
TargetMol Chemical Structure Sofosbuvir impurity H
Sofosbuvir impurity H, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is a diastereoisomer of Sofosbuvir.Sofosbuvir is an...
T10067 2',5-Difluoro-2'-deoxycytidine
化合物 T10067
581772-30-7 98%
TargetMol Chemical Structure 2',5-Difluoro-2'-deoxycytidine
2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA.
T12967 Sofosbuvir impurity L
化合物 T12967
T12967 98%
TargetMol Chemical Structure Sofosbuvir impurity L
Sofosbuvir impurity L is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
T12968 Sofosbuvir impurity M
索非布韦杂质 M
2095551-10-1 98%
TargetMol Chemical Structure Sofosbuvir impurity M
Sofosbuvir impurity M is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
T73223 NS5A-IN-3
化合物 NS5A-IN-3
2764786-56-1 98%
TargetMol Chemical Structure NS5A-IN-3
NS5A-IN-3 (Compound 15) 为高效NS5A抑制剂,对HCV基因型1b显示出高效力,并对基因型3a (GT 3a) 活性提升以及展现出良好的代谢稳定性。NS5A-IN-3相较于daclatasvir,对基因型1b具有更高的耐药门槛。
T73834 NS5A-IN-2
化合物 NS5A-IN-2
2764786-74-3 98%
TargetMol Chemical Structure NS5A-IN-2
NS5A-IN-2 (Compound 33)为一种高效的NS5A抑制剂,对HCV基因型1b展现出极高效力,并对基因型3a (GT 3a) 亦具备增强活性与良好的代谢稳定性。
T16675 PSI-352938
化合物 T16675
1231747-17-3 98%
TargetMol Chemical Structure PSI-352938
PSI-352938 is an inhibitor of hepatitis C virus nucleotide.
TN3438 Arborinine
化合物 TN3438
5489-57-6 98%
TargetMol Chemical Structure Arborinine
Arborinine shows mild in vitro antibacterial activity, it possesses moderate levels of anti-hepatitis C virus(HCV) activities with the IC50 values being 6.4 ± 0....
TN5079 Sulochrin
化合物 TN5079
519-57-3 98%
TargetMol Chemical Structure Sulochrin
Sulochrin shows antifungal and antibacterial activities, it can inhibit hepatitis C virus (HCV) infection in a dose-dependent manner without any apparent cytotox...
T13281 Valopicitabine
化合物 T13281
640281-90-9 98%
TargetMol Chemical Structure Valopicitabine
Valopicitabine is an effective prodrug of the effective anti-HCV drug 2'-C-methylcytidine and can be used as a promising antiviral drug for the study of chronic ...
TQ0122 VCH-916
化合物VCH-916
1200133-34-1 98%
TargetMol Chemical Structure VCH-916
VCH-916 是一种新型非核苷类 HCV NS5B 聚合酶抑制剂。
Sennidin A
TN1033
Sennidin A 是从狭叶番泻分离得到的一种天然产物,能够抑制 HCV NS3 解旋酶,其 IC50值为0.8 μM。它诱导 Akt 和葡萄糖转运蛋白4的磷酸化,刺激葡萄糖掺入。
γ-Fagarine
TN1138
gamma-Fagarine possesses moderate levels of anti-HCV activities with IC50 values being 20.4 ± 0.4 ug/ml, respectively. It has sister chromatid exchanges (SCEs)-i...
Sennidin B
TN1034
Sennidin B 是从Cassia angustifolia 分离得到的Sennidin A 异构体,它刺激葡萄糖掺入,诱导Akt 和葡萄糖转运蛋白4 的磷酸化。
GS-443902
T5539
Remdesivir triphosphate 是一种有效的病毒 RNA 依赖的 RNA 聚合酶抑制剂,对RSVRdRp 和 HCVRdRp 的IC50分别为 1.1 µM 和 5 µM。它是 Remdesivir 的活性三磷酸代谢物。
Dehydrojuncusol
TN3809
Dehydrojuncusol, a new inhibitor of hepatitis C virus RNA replication, it inhibits infection of different HCV genotypes by targeting the NS5A protein and is acti...
Sofosbuvir impurity K
T12966
Sofosbuvir impurity K is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
Sofosbuvir impurity N
T12969
Sofosbuvir impurity N is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
Micrococcin P1
T12033
Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor(EC50 range of 0.1-0.5 μM)
Sofosbuvir impurity J
T12965
Sofosbuvir impurity J is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
Sofosbuvir impurity H
T12963
Sofosbuvir impurity H, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is a diastereoisomer of Sofosbuvir.Sofosbuvir is an...
2',5-Difluoro-2'-deoxycytidine
T10067
2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA.
Sofosbuvir impurity L
T12967
Sofosbuvir impurity L is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
Sofosbuvir impurity M
T12968
Sofosbuvir impurity M is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
NS5A-IN-3
T73223
NS5A-IN-3 (Compound 15) 为高效NS5A抑制剂,对HCV基因型1b显示出高效力,并对基因型3a (GT 3a) 活性提升以及展现出良好的代谢稳定性。NS5A-IN-3相较于daclatasvir,对基因型1b具有更高的耐药门槛。
NS5A-IN-2
T73834
NS5A-IN-2 (Compound 33)为一种高效的NS5A抑制剂,对HCV基因型1b展现出极高效力,并对基因型3a (GT 3a) 亦具备增强活性与良好的代谢稳定性。
PSI-352938
T16675
PSI-352938 is an inhibitor of hepatitis C virus nucleotide.
Arborinine
TN3438
Arborinine shows mild in vitro antibacterial activity, it possesses moderate levels of anti-hepatitis C virus(HCV) activities with the IC50 values being 6.4 ± 0....
Sulochrin
TN5079
Sulochrin shows antifungal and antibacterial activities, it can inhibit hepatitis C virus (HCV) infection in a dose-dependent manner without any apparent cytotox...
Valopicitabine
T13281
Valopicitabine is an effective prodrug of the effective anti-HCV drug 2'-C-methylcytidine and can be used as a promising antiviral drug for the study of chronic ...
VCH-916
TQ0122
VCH-916 是一种新型非核苷类 HCV NS5B 聚合酶抑制剂。
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TargetMol Loading
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