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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
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Cat. No. Product Name CAS No. Purity Chemical Structure
TQ0030 Tomeglovir
托美洛韦
233254-24-5 98%
TargetMol Chemical Structure Tomeglovir
Tomeglovir is a potent anti-CMV agent, inhibiting the processing of viral DNA-concatemers (IC50s: 0.34/0.039 μM for HCMV and MCMV).
T71653 GS-9256
化合物 GS-9256
1001094-46-7 98%
TargetMol Chemical Structure GS-9256
GS-9256为选择性HCV NS3蛋白酶抑制剂,展现出优良的药代动力学特性及抗病毒活性。
T14095 ACH-806
化合物 T14095
870142-71-5 98%
TargetMol Chemical Structure ACH-806
ACH-806 is an NS4A antagonist. It can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.
TN1703 Glycyrin
格里西轮
66056-18-6 98%
TargetMol Chemical Structure Glycyrin
Glycyrin, one of the main PPAR-gamma ligands of licorice, can significantly decrease the blood glucose levels of genetically diabetic KK-A(y) mice.
T12964 Sofosbuvir impurity I
化合物 T12964
T12964 98%
TargetMol Chemical Structure Sofosbuvir impurity I
Sofosbuvir impurity I is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
T12956 Sofosbuvir impurity A
索非布韦杂质A
1496552-16-9 98%
TargetMol Chemical Structure Sofosbuvir impurity A
Sofosbuvir impurity A is an diastereoisomer of Sofosbuvir. Sofosbuvir is anHCV RNA replication inhibitor ,with potent anti-hepatitis C virus activity.
TN4404 Ladanein
化合物 TN4404
10176-71-3 98%
TargetMol Chemical Structure Ladanein
Ladanein is a phytochemicals inhibitor that is known to disrupt the interactions of core and other hepatitis C virus (HCV) proteins.Ladanein possesses free radic...
T14555 BI-1230
化合物 T14555
849022-32-8 98%
TargetMol Chemical Structure BI-1230
BI-1230 is a potent inhibitor of HCV NS3 protease, exhibiting efficacy in the low nanomolar range, and notably suppresses viral replication. This compound demons...
TN6732 Oenothein B
月见草素B
104987-36-2 98%
TargetMol Chemical Structure Oenothein B
Oenothein B 是一种聚(ADP-核糖)糖水解酶的特异性抑制剂。 Oenothein B 具有抗氧化、抗炎、抗真菌、抗 HCV 和抗肿瘤特性。
T16774 RO-9187
化合物 T16774
876708-03-1 98%
TargetMol Chemical Structure RO-9187
RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).
T1188 Mizoribine
咪唑立宾
50924-49-7 99.98%
TargetMol Chemical Structure Mizoribine
Mizoribine (NSC-289637) 是一种免疫抑制剂,抑制HCVRNA 复制,有抗 HCV 活性,IC50约为 100 μM。它抑制SARS-CoV 复制,对 SARS-CoV Frankfurt-1 和 SARS-CoV HKU39849 的 IC50分别为 3.5 μg/mL 和 16 μg/mL。
T5S1598 Mulberroside C
桑皮苷 C
102841-43-0 99.97%
TargetMol Chemical Structure Mulberroside C
Mulberroside C 是桑树中的主要生物活性成分之一,可抑制 HCV 复制,具有抗病毒活性。
T9577 HCV-IN-31
化合物HCV-IN-31
1998705-62-6 99.95%
TargetMol Chemical Structure HCV-IN-31
HCV-IN-31 是一种HCV 抑制剂,EC50/EC95值为15.7 μM。
T22489 2'-MeCCPA
化合物2'-MeCCPA
205171-12-6 99.93%
TargetMol Chemical Structure 2'-MeCCPA
2'-MeCCPA 是一种具有有效性和高选择性的 A1 腺苷受体 (A1AR) 激动剂,对 AR 的 K 值为 1.8 nM。2'-MeCCPA 抑制毛喉素刺激的腺苷酸环化酶活性,IC值为13.1 nM。2'-MeCCPA 具有镇痛活性,可用于研究 HCV 。
T6846 Vesatolimod
维沙莫德
1228585-88-3 99.92%
TargetMol Chemical Structure Vesatolimod
Vesatolimod (GS-9620) 是一种选择性 Toll 样受体 7 口服激动剂,EC50值为291 nM。
T4474 Asunaprevir
阿那匹韦
630420-16-5 99.92%
TargetMol Chemical Structure Asunaprevir
Asunaprevir (BMS-650032) 是一种有口服活性的 HCV NS3 蛋白酶抑制剂,IC50值为 0.2 nM-3.5 nM。它也是 SARS-CoV-2 3CLpro 抑制剂。
T1822L Clemizole hydrochloride
盐酸克立咪唑
1163-36-6 99.91%
TargetMol Chemical Structure Clemizole hydrochloride
Clemizole hydrochloride 是一种 TRPC5通道的抑制剂。它还是一种 H1 组胺受体拮抗剂,抑制 HCV 复制。
T3334 Velpatasvir
维帕他韦
1377049-84-7 99.91%
TargetMol Chemical Structure Velpatasvir
Velpatasvir (GS-5816) 是一种的 HCV NS5A 抑制剂。它也是 SARS-CoV 3CLpro 的抑制剂,IC50为 2.16 μM。
T3810 Saikosaponin B2
柴胡皂苷 B2
58316-41-9 99.88%
TargetMol Chemical Structure Saikosaponin B2
Saikosaponin B2 是从柴胡根中分离得到的一种活性成分,可抑制 HCV 病毒感染的侵入,有抗癌作用。
T3001 Honokiol
和厚朴酚
35354-74-6 99.87%
TargetMol Chemical Structure Honokiol
Honokiol (NSC-293100) 是厚朴提取物的活性成分,靶向多种信号分子,具有抗氧化,抗炎,抗血管生成和抗癌活性。它可抑制 Akt 的激活并增强 ERK1/ERK2 的磷酸化。
Tomeglovir
TQ0030
Tomeglovir is a potent anti-CMV agent, inhibiting the processing of viral DNA-concatemers (IC50s: 0.34/0.039 μM for HCMV and MCMV).
GS-9256
T71653
GS-9256为选择性HCV NS3蛋白酶抑制剂,展现出优良的药代动力学特性及抗病毒活性。
ACH-806
T14095
ACH-806 is an NS4A antagonist. It can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.
Glycyrin
TN1703
Glycyrin, one of the main PPAR-gamma ligands of licorice, can significantly decrease the blood glucose levels of genetically diabetic KK-A(y) mice.
Sofosbuvir impurity I
T12964
Sofosbuvir impurity I is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.
Sofosbuvir impurity A
T12956
Sofosbuvir impurity A is an diastereoisomer of Sofosbuvir. Sofosbuvir is anHCV RNA replication inhibitor ,with potent anti-hepatitis C virus activity.
Ladanein
TN4404
Ladanein is a phytochemicals inhibitor that is known to disrupt the interactions of core and other hepatitis C virus (HCV) proteins.Ladanein possesses free radic...
BI-1230
T14555
BI-1230 is a potent inhibitor of HCV NS3 protease, exhibiting efficacy in the low nanomolar range, and notably suppresses viral replication. This compound demons...
Oenothein B
TN6732
Oenothein B 是一种聚(ADP-核糖)糖水解酶的特异性抑制剂。 Oenothein B 具有抗氧化、抗炎、抗真菌、抗 HCV 和抗肿瘤特性。
RO-9187
T16774
RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).
Mizoribine
T1188
Mizoribine (NSC-289637) 是一种免疫抑制剂,抑制HCVRNA 复制,有抗 HCV 活性,IC50约为 100 μM。它抑制SARS-CoV 复制,对 SARS-CoV Frankfurt-1 和 SARS-CoV HKU39849 的 IC50分别为 3.5 μg/mL 和 16 μg/mL。
Mulberroside C
T5S1598
Mulberroside C 是桑树中的主要生物活性成分之一,可抑制 HCV 复制,具有抗病毒活性。
HCV-IN-31
T9577
HCV-IN-31 是一种HCV 抑制剂,EC50/EC95值为15.7 μM。
2'-MeCCPA
T22489
2'-MeCCPA 是一种具有有效性和高选择性的 A1 腺苷受体 (A1AR) 激动剂,对 AR 的 K 值为 1.8 nM。2'-MeCCPA 抑制毛喉素刺激的腺苷酸环化酶活性,IC值为13.1 nM。2'-MeCCPA 具有镇痛活性,可用于研究 HCV 。
Vesatolimod
T6846
Vesatolimod (GS-9620) 是一种选择性 Toll 样受体 7 口服激动剂,EC50值为291 nM。
Asunaprevir
T4474
Asunaprevir (BMS-650032) 是一种有口服活性的 HCV NS3 蛋白酶抑制剂,IC50值为 0.2 nM-3.5 nM。它也是 SARS-CoV-2 3CLpro 抑制剂。
Clemizole hydrochloride
T1822L
Clemizole hydrochloride 是一种 TRPC5通道的抑制剂。它还是一种 H1 组胺受体拮抗剂,抑制 HCV 复制。
Velpatasvir
T3334
Velpatasvir (GS-5816) 是一种的 HCV NS5A 抑制剂。它也是 SARS-CoV 3CLpro 的抑制剂,IC50为 2.16 μM。
Saikosaponin B2
T3810
Saikosaponin B2 是从柴胡根中分离得到的一种活性成分,可抑制 HCV 病毒感染的侵入,有抗癌作用。
Honokiol
T3001
Honokiol (NSC-293100) 是厚朴提取物的活性成分,靶向多种信号分子,具有抗氧化,抗炎,抗血管生成和抗癌活性。它可抑制 Akt 的激活并增强 ERK1/ERK2 的磷酸化。
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