vidarabine [Ligand Id: 4806] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL1090 (ARA-A, Arabinosyladenine, Arasena-a, CI 673, CI-673, NSC-247519, NSC-404241, NSC-757383, Vidarabine, Vidarabine anhydrous, Vidarabine, anhydrous, Vidarabine monohydrate, Vira-a)
  • S-Adenosylhomocysteine hydrolase/Adenosylhomocysteinase in Mouse [ChEMBL: CHEMBL2389] [GtoPdb: 1233] [UniProtKB: P50247]
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  • adenylyl cyclase 5/Adenylate cyclase type V in Rat [ChEMBL: CHEMBL2880] [GtoPdb: 1282] [UniProtKB: Q04400]
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  • dipeptidyl peptidase 4/Dipeptidyl peptidase IV in Human [ChEMBL: CHEMBL284] [GtoPdb: 1612] [UniProtKB: P27487]
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  • Hepatitis C virus NS5B RNA-dependent RNA polymerase in Hepatitis C virus [ChEMBL: CHEMBL5375] [UniProtKB: Q8JXU8]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
S-Adenosylhomocysteine hydrolase/Adenosylhomocysteinase in Mouse (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2389] [GtoPdb: 1233] [UniProtKB: P50247]
ChEMBL Activity determined in mouse liver S-adenosyl-L-homocysteine hydrolase and expressed as KI values. B 4.52 pKi 30000 nM Ki J Med Chem (1991) 34: 647-656 [PMID:1995889]
adenylyl cyclase 5/Adenylate cyclase type V in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2880] [GtoPdb: 1282] [UniProtKB: Q04400]
ChEMBL Compound was evaluated for inhibition of adenylate cyclase from rat brain B 4.09 pIC50 82000 nM IC50 J Med Chem (2004) 47: 1207-1213 [PMID:14971900]
dipeptidyl peptidase 4/Dipeptidyl peptidase IV in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL284] [GtoPdb: 1612] [UniProtKB: P27487]
ChEMBL Inhibition of human DPP4 from human Caco-2 cells B 7.21 pIC50 62 nM IC50 J Med Chem (2010) 53: 559-572 [PMID:20000418]
Hepatitis C virus NS5B RNA-dependent RNA polymerase in Hepatitis C virus (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5375] [UniProtKB: Q8JXU8]
ChEMBL Inhibition HCV NS5B-mediated RNA synthesis F 4.3 pIC50 50000 nM IC50 J Med Chem (2004) 47: 2283-2295 [PMID:15084127]
ChEMBL Inhibition HCV RNA replication F 4.3 pEC50 >50000 nM EC50 J Med Chem (2004) 47: 2283-2295 [PMID:15084127]

ChEMBL data shown on this page come from version 34:

Zdrazil B, Felix E, Hunter F, Manners EJ, Blackshaw J, Corbett S, de Veij M, Ioannidis H, Lopez DM, Mosquera JF, Magarinos MP, Bosc N, Arcila R, Kizilören T, Gaulton A, Bento AP, Adasme MF, Monecke P, Landrum GA, Leach AR. (2024). The ChEMBL Database in 2023: a drug discovery platform spanning multiple bioactivity data types and time periods. Nucleic Acids Res., 52(D1). DOI: 10.1093/nar/gkad1004. [EPMCID:10767899] [PMID:37933841]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]