Found 29 hits for monomerid = 50115579 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
PA/PB1
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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| PDB Article PubMed
| 480 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
University of Tennessee Health Science Center
Curated by ChEMBL
| Assay Description Binding affinity to PA N-terminal domain (Competitive) |
ACS Chem Biol 7: 526-34 (2012)
Article DOI: 10.1021/cb200439z BindingDB Entry DOI: 10.7270/Q2JQ121G |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Carbonic anhydrase 1
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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| Article PubMed
| 3.35E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ di Sassari
Curated by ChEMBL
| Assay Description Inhibition of human CA1 using CO2 as substrate incubated for 6 hrs prior to substrate addition measured for 10 to 100 secs by stopped flow technique |
Bioorg Med Chem Lett 22: 5801-6 (2012)
Article DOI: 10.1016/j.bmcl.2012.07.094 BindingDB Entry DOI: 10.7270/Q2319X0G |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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| Article PubMed
| 4.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ di Sassari
Curated by ChEMBL
| Assay Description Inhibition of human CA2 using CO2 as substrate incubated for 6 hrs prior to substrate addition measured for 10 to 100 secs by stopped flow technique |
Bioorg Med Chem Lett 22: 5801-6 (2012)
Article DOI: 10.1016/j.bmcl.2012.07.094 BindingDB Entry DOI: 10.7270/Q2319X0G |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 9
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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| Article PubMed
| 6.79E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ di Sassari
Curated by ChEMBL
| Assay Description Inhibition of human CA9 using CO2 as substrate incubated for 6 hrs prior to substrate addition measured for 10 to 100 secs by stopped flow technique |
Bioorg Med Chem Lett 22: 5801-6 (2012)
Article DOI: 10.1016/j.bmcl.2012.07.094 BindingDB Entry DOI: 10.7270/Q2319X0G |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 12
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 7.75E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ di Sassari
Curated by ChEMBL
| Assay Description Inhibition of human CA12 using CO2 as substrate incubated for 6 hrs prior to substrate addition measured for 10 to 100 secs by stopped flow technique |
Bioorg Med Chem Lett 22: 5801-6 (2012)
Article DOI: 10.1016/j.bmcl.2012.07.094 BindingDB Entry DOI: 10.7270/Q2319X0G |
More data for this Ligand-Target Pair | |
Hepatitis C virus NS5B RNA-dependent RNA polymerase
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | UniProtKB/TrEMBL
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| Article PubMed
| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Italy. Vinc
Curated by ChEMBL
| Assay Description Inhibitory concentration required to inhibit HCV RNA dependent RNA polymerase Nonstructural protein 5B is determined |
J Med Chem 47: 5336-9 (2004)
Article DOI: 10.1021/jm0494669 BindingDB Entry DOI: 10.7270/Q2G1609M |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 reverse transcriptase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
B.MOAD DrugBank GoogleScholar AffyNet
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| Article PubMed
| n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Université des Sciences et Technologies de Lille
Curated by ChEMBL
| Assay Description Concentration required to inhibit strand transfer of HIV-1 integrase using Mn2+ as a divalent cation source. |
J Med Chem 47: 5583-6 (2004)
Article DOI: 10.1021/jm0408464 BindingDB Entry DOI: 10.7270/Q2JS9PX9 |
More data for this Ligand-Target Pair | |
Hepatitis C virus NS5B RNA-dependent RNA polymerase
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | UniProtKB/TrEMBL
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| Article PubMed
| n/a | n/a | 5.60E+3 | n/a | n/a | n/a | n/a | 7.5 | n/a |
University of Rome La Sapienza
Curated by ChEMBL
| Assay Description Inhibitory concentration against NS5B HCV polymerase using [alpha-32P]UTP as radioligand (30 degree C for 2 h, at pH 7.5 with Tris-HCl buffer) |
J Med Chem 48: 6304-14 (2005)
Article DOI: 10.1021/jm0504454 BindingDB Entry DOI: 10.7270/Q2T43SNM |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
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Similars
| Article PubMed
| n/a | n/a | 2.42E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università di Messina
Curated by ChEMBL
| Assay Description Strand transfer inhibitory activity against HIV-1 integrase |
J Med Chem 48: 7084-8 (2005)
Article DOI: 10.1021/jm050549e BindingDB Entry DOI: 10.7270/Q27W6BR1 |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
B.MOAD DrugBank GoogleScholar AffyNet
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| Article PubMed
| n/a | n/a | >3.33E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Università di Sassari
Curated by ChEMBL
| Assay Description Inhibition of HIV1 integrase 3' processing activity |
J Med Chem 49: 4248-60 (2006)
Article DOI: 10.1021/jm060193m BindingDB Entry DOI: 10.7270/Q2T15384 |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
B.MOAD DrugBank GoogleScholar AffyNet
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Similars
| Article PubMed
| n/a | n/a | 6.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università di Sassari
Curated by ChEMBL
| Assay Description Inhibition of HIV1 integrase strand transfer activity |
J Med Chem 49: 4248-60 (2006)
Article DOI: 10.1021/jm060193m BindingDB Entry DOI: 10.7270/Q2T15384 |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
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| Article PubMed
| n/a | n/a | 8.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università di Sassari
Curated by ChEMBL
| Assay Description Inhibition of HIV1 integrase 3' processing activity in presence of exogenous cobalt ion |
J Med Chem 49: 4248-60 (2006)
Article DOI: 10.1021/jm060193m BindingDB Entry DOI: 10.7270/Q2T15384 |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
B.MOAD DrugBank GoogleScholar AffyNet
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Patents
Similars
| Article PubMed
| n/a | n/a | 8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Università di Sassari
Curated by ChEMBL
| Assay Description Inhibition of HIV1 integrase strand transfer activity in presence of exogenous cobalt ion |
J Med Chem 49: 4248-60 (2006)
Article DOI: 10.1021/jm060193m BindingDB Entry DOI: 10.7270/Q2T15384 |
More data for this Ligand-Target Pair | |
PA/PB1
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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Patents
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| PDB Article PubMed
| n/a | n/a | 2.13E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Discovery Welwyn
Curated by ChEMBL
| Assay Description Inhibitory concentration against cap-dependent endonuclease activity of influenza virus RNP |
J Med Chem 46: 1153-64 (2003)
Article DOI: 10.1021/jm020334u BindingDB Entry DOI: 10.7270/Q22J6B6V |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Flap endonuclease 1
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD antibodypedia GoogleScholar AffyNet
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| Article PubMed
| n/a | n/a | 2.49E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Athersys, Inc.
Curated by ChEMBL
| Assay Description Concentration required for 50% inhibition of Flap endonuclease-1 |
Bioorg Med Chem Lett 14: 4915-8 (2004)
Article DOI: 10.1016/j.bmcl.2004.07.028 BindingDB Entry DOI: 10.7270/Q2ZC82BF |
More data for this Ligand-Target Pair | |
DNA excision repair protein ERCC-5
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
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Patents
Similars
| Article PubMed
| n/a | n/a | 7.54E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Athersys, Inc.
Curated by ChEMBL
| Assay Description Concentration required for 50% inhibition of Xeroderma pigmentosum G |
Bioorg Med Chem Lett 14: 4915-8 (2004)
Article DOI: 10.1016/j.bmcl.2004.07.028 BindingDB Entry DOI: 10.7270/Q2ZC82BF |
More data for this Ligand-Target Pair | |
Protein-tyrosine phosphatase 1B
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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Patents
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| Article PubMed
| n/a | n/a | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Max-Planck-Institute of Molecular Physiology
Curated by ChEMBL
| Assay Description Inhibition of PTP1B |
Bioorg Med Chem 19: 2145-55 (2011)
Article DOI: 10.1016/j.bmc.2011.02.047 BindingDB Entry DOI: 10.7270/Q2BR8SHK |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
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Patents
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| PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
National Cancer Institute/NIH
Curated by ChEMBL
| Assay Description Inhibitory effect on 3'-processing(3'-P) of proviral DNA in an extracellular HIV-1 integrase assay |
J Med Chem 45: 3184-94 (2002)
BindingDB Entry DOI: 10.7270/Q26D5TPD |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
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Patents
Similars
| PubMed
| n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
National Cancer Institute/NIH
Curated by ChEMBL
| Assay Description Inhibitory effect on strand transfer of proviral DNA into host DNA in an extracellular HIV-1 integrase assay in experiment 2 |
J Med Chem 45: 3184-94 (2002)
BindingDB Entry DOI: 10.7270/Q26D5TPD |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
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Patents
Similars
| PubMed
| n/a | n/a | 2.42E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
National Cancer Institute/NIH
Curated by ChEMBL
| Assay Description Inhibitory effect on strand transfer of proviral DNA into host DNA in an extracellular HIV-1 integrase assay in experiment 1 |
J Med Chem 45: 3184-94 (2002)
BindingDB Entry DOI: 10.7270/Q26D5TPD |
More data for this Ligand-Target Pair | |
Genome polyprotein
(Hepatitis C virus (HCV)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB
UniProtKB/SwissProt
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Patents
Similars
| Article PubMed
| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Wollongong
Curated by ChEMBL
| Assay Description Inhibitory concentration against hepatitis C virus polymerase |
J Med Chem 48: 1-20 (2005)
Article DOI: 10.1021/jm0400101 BindingDB Entry DOI: 10.7270/Q2XP75Q1 |
More data for this Ligand-Target Pair | |
PA/PB1
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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Patents
Similars
| PDB Article PubMed
| n/a | n/a | n/a | n/a | 2.07E+3 | n/a | n/a | n/a | n/a |
University of Tennessee Health Science Center
Curated by ChEMBL
| Assay Description Plaque growth inhibition |
ACS Chem Biol 7: 526-34 (2012)
Article DOI: 10.1021/cb200439z BindingDB Entry DOI: 10.7270/Q2JQ121G |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
PA/PB1
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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Patents
Similars
| PDB PubMed
| n/a | n/a | 2.13E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description Inhibition of cap 1 ALMV primed Influenza transcriptase |
Antimicrob Agents Chemother 38: 2827-37 (1995)
BindingDB Entry DOI: 10.7270/Q25H7HBP |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Hepatitis C virus NS5B RNA-dependent RNA polymerase
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | UniProtKB/TrEMBL
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Patents
Similars
| Article PubMed
| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
MRL Rome
Curated by ChEMBL
| Assay Description inhibitory concentration against RNA dependent RNA polymerase Nonstructural protein 5B of hepatitis C virus |
Bioorg Med Chem Lett 14: 5085-8 (2004)
Article DOI: 10.1016/j.bmcl.2004.07.075 BindingDB Entry DOI: 10.7270/Q27P8XV3 |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 integrase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
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Patents
Similars
| Article PubMed
| n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
NCI-Frederick
Curated by ChEMBL
| Assay Description Inhibition of Integrase catalyzed strand transfer (ST) as measured in an in vitro assay |
Bioorg Med Chem Lett 14: 1205-7 (2004)
Article DOI: 10.1016/j.bmcl.2003.12.064 BindingDB Entry DOI: 10.7270/Q23X8628 |
More data for this Ligand-Target Pair | |
Human immunodeficiency virus type 1 reverse transcriptase
(Human immunodeficiency virus 1) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB MMDB
UniProtKB/TrEMBL
B.MOAD DrugBank GoogleScholar AffyNet
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CHEMBL KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 5.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Italy. Vinc
Curated by ChEMBL
| Assay Description Inhibitory activity of the compound against HIV-1 reverse transcriptase was determined |
J Med Chem 47: 14-7 (2003)
Article DOI: 10.1021/jm0342109 BindingDB Entry DOI: 10.7270/Q2736QB8 |
More data for this Ligand-Target Pair | |
Polymerase acidic protein
(Influenza A virus (strain A/X-31 H3N2)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB
UniProtKB/SwissProt
GoogleScholar AffyNet
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CHEMBL KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| PDB Article PubMed
| n/a | n/a | 3.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Polo Universitario SS. Annunziata
Curated by ChEMBL
| Assay Description Inhibition of recombinant Influenza A virus (A/X-31(H3N2)) N-terminal 6xHis-tagged PA-Nter (1 to 217 residues) expressed in Escherichia coli BL21-Cod... |
Bioorg Med Chem 26: 4544-4550 (2018)
Article DOI: 10.1016/j.bmc.2018.07.046 BindingDB Entry DOI: 10.7270/Q2TM7DS6 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
GlcB
(Homo sapiens (Human)) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | PDB
GoogleScholar AffyNet
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CHEMBL KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| PDB D3R
| n/a | n/a | 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
D3R
| Assay Description DNTB-Coupled_Enzyme_Assay |
D3R 223: (2015)
BindingDB Entry DOI: 10.7270/Q2NC602G |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Hepatitis C virus NS5B RNA-dependent RNA polymerase
(Hepatitis C virus) | BDBM50115579
((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)Show InChI InChI=1S/C10H8O4/c11-8(6-9(12)10(13)14)7-4-2-1-3-5-7/h1-5H,6H2,(H,13,14) | UniProtKB/TrEMBL
B.MOAD GoogleScholar AffyNet
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CHEMBL KEGG MMDB PC cid PC sid PDB UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Italy. Vinc
Curated by ChEMBL
| Assay Description Inhibitory activity against Hepatitis C virus RNA dependent RNA polymerase nonstructural protein 5B |
J Med Chem 47: 14-7 (2003)
Article DOI: 10.1021/jm0342109 BindingDB Entry DOI: 10.7270/Q2736QB8 |
More data for this Ligand-Target Pair | |