Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T03896 | Target Info | |||
Target Name | Hepatitis C virus Serine protease NS3/4A (HCV NS3/4A) | ||||
Synonyms |
HCV Hepacivirin/NS4A; HCV NS3P/NS4A; HCV p70/NS4A
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Target Type | Successful Target | ||||
Gene Name | HCV NS3/4A | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Pancreatic elastase 1 (CELA1) | Successful Target | ||||
UniProt ID | CELA1_HUMAN | |||||
Gene Name | CELA1 | |||||
Synonyms |
Elastase; CELA1
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Representative Drug(s) | Drug Info | IC50 = 30 nM | [1] | |||
Co-Target Name | Coagulation factor IIa (F2) | Successful Target | ||||
UniProt ID | THRB_HUMAN | |||||
Gene Name | F2 | |||||
Synonyms |
Prothrombin; Coagulation factor II
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Representative Drug(s) | Drug Info | IC50 < 1000 nM | Click to Show More | [2] | ||
2 | Drug Info | IC50 < 1000 nM | [2] | |||
Co-Target Name | Chymase (CYM) | Clinical trial Target | ||||
UniProt ID | CMA1_HUMAN | |||||
Gene Name | CMA1 | |||||
Synonyms |
Mast cell protease I; CYH; Alpha-chymase
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Representative Drug(s) | Drug Info | IC50 = 26 nM | Click to Show More | [1] | ||
2 | Drug Info | IC50 = 32 nM | [1] | |||
Co-Target Name | Cathepsin K (CTSK) | Clinical trial Target | ||||
UniProt ID | CATK_HUMAN | |||||
Gene Name | CTSK | |||||
Synonyms |
Cathepsin X; Cathepsin O2; Cathepsin O; CTSO2; CTSO
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Representative Drug(s) | Drug Info | IC50 = 40 nM | Click to Show More | [1] | ||
2 | Drug Info | IC50 = 630 nM | [1] | |||
Co-Target Name | Cathepsin S (CTSS) | Clinical trial Target | ||||
UniProt ID | CATS_HUMAN | |||||
Gene Name | CTSS | |||||
Synonyms |
Cysteine protease cathepsin S
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Representative Drug(s) | Drug Info | IC50 = 120 nM | Click to Show More | [1] | ||
2 | Drug Info | IC50 = 300 nM | [1] | |||
3 | Simeprevir | Drug Info | IC50 = 800 nM | [4] | ||
Co-Target Name | Neutrophil elastase (NE) | Clinical trial Target | ||||
UniProt ID | ELNE_HUMAN | |||||
Gene Name | ELANE | |||||
Synonyms |
PMN elastase; Medullasin; Human leukocyte elastase; HLE; Elastase-2; ELA2; Bone marrow serine protease
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Representative Drug(s) | Drug Info | IC50 = 680 nM | [3] | |||
Co-Target Name | Cathepsin L (CTSL) | Clinical trial Target | ||||
UniProt ID | CATL1_HUMAN | |||||
Gene Name | CTSL | |||||
Synonyms |
Major excreted protein; MEP; Cathepsin L1; CTSL1
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Representative Drug(s) | Drug Info | IC50 = 760 nM | [1] | |||
Co-Target Name | Cathepsin V (CTSV) | Patented-recorded Target | ||||
UniProt ID | CATL2_HUMAN | |||||
Gene Name | CTSV | |||||
Synonyms |
UNQ268/PRO305; Cathepsin U; Cathepsin L2; CTSU; CTSL2; CATL2
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Representative Drug(s) | Drug Info | IC50 = 75 nM | [1] | |||
Co-Target Name | Cathepsin B (CTSB) | Patented-recorded Target | ||||
UniProt ID | CATB_HUMAN | |||||
Gene Name | CTSB | |||||
Synonyms |
Ctsb; Cathepsins B; Cathepsin-B; Cathepsin B1; CPSB; APPS; APP secretase
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Representative Drug(s) | Drug Info | IC50 = 210 nM | [5] |
References | Top | ||||
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REF 1 | MK-7009, a potent and selective inhibitor of hepatitis C virus NS3/4A protease. Antimicrob Agents Chemother. 2010 Jan;54(1):305-11. | ||||
REF 2 | Azetidines and spiro azetidines as novel P2 units in hepatitis C virus NS3 protease inhibitors. Bioorg Med Chem Lett. 2013 Dec 1;23(23):6325-30. | ||||
REF 3 | Preclinical characterization of BI 201335, a C-terminal carboxylic acid inhibitor of the hepatitis C virus NS3-NS4A protease. Antimicrob Agents Chemother. 2010 Nov;54(11):4611-8. | ||||
REF 4 | In vitro activity and preclinical profile of TMC435350, a potent hepatitis C virus protease inhibitor. Antimicrob Agents Chemother. 2009 Apr;53(4):1377-85. | ||||
REF 5 | Synopsis of some recent tactical application of bioisosteres in drug design. J Med Chem. 2011 Apr 28;54(8):2529-91. |
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