Found 19 hits for monomerid = 50303499 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 |
Carbonic anhydrase 7
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 2.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 7 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic Anhydrase VA
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | Reactome pathway KEGG
UniProtKB/SwissProt
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| Article PubMed
| 5.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 5A by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 6 (CA-VI)
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB
UniProtKB/SwissProt
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| Article PubMed
| 5.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 6 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 1
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
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| Article PubMed
| 5.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 1 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 4
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
Reactome pathway KEGG
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| Article PubMed
| 8.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 4 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 15
(Mus musculus) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | KEGG
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| 8.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of mouse carbonic anhydrase 15 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic Anhydrase XIII
(Mus musculus (mouse)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
Reactome pathway KEGG
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| Article PubMed
| 8.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of mouse carbonic anhydrase 13 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic Anhydrase XIV
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB
Reactome pathway KEGG
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| Article PubMed
| 9.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 14 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 12
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
Reactome pathway KEGG
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| Article PubMed
| 9.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 12 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 9
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
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| Article PubMed
| 9.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 9 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic Anhydrase III
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
Reactome pathway KEGG
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| Article PubMed
| 9.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 3 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
Reactome pathway KEGG
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| Article PubMed
| >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 2 by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Carbonic Anhydrase VB
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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CHEMBL KEGG PC cid PC sid PDB UniChem
Patents
Similars
| Article PubMed
| >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universita degli Studi di Firenze
Curated by ChEMBL
| Assay Description Inhibition of human carbonic anhydrase 5B by stopped flow CO2 hydration assay |
J Med Chem 53: 335-44 (2010)
Article DOI: 10.1021/jm901287j BindingDB Entry DOI: 10.7270/Q2MS3TP5 |
More data for this Ligand-Target Pair | |
Cytochrome P450 19A1
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
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| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Health Sciences University of Hokkaido
Curated by ChEMBL
| Assay Description Inhibition of CYP19 in human placental microsome using [1beta-3H]-androstenedione as substrate after 15 mins in presence of NADPH by liquid scintilla... |
Bioorg Med Chem Lett 27: 2645-2649 (2017)
Article DOI: 10.1016/j.bmcl.2017.01.062 BindingDB Entry DOI: 10.7270/Q2CF9SH5 |
More data for this Ligand-Target Pair | |
Aldose reductase (AR)
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
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| Article PubMed
| n/a | n/a | 6.75E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Toyama
Curated by ChEMBL
| Assay Description Inhibition human recombinant aldose reductase 1 by spectrophotometric analysis |
Bioorg Med Chem Lett 20: 5630-3 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.038 BindingDB Entry DOI: 10.7270/Q28052TK |
More data for this Ligand-Target Pair | |
Exportin-1
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
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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 |
Osaka University
Curated by ChEMBL
| Assay Description Inhibition of CRM1-mediated hemagglutinin-tagged HIV1 Rev protein nuclear export in human HeLa cells assessed as nucleus localization after 12 hrs by... |
Bioorg Med Chem Lett 20: 3717-20 (2010)
Article DOI: 10.1016/j.bmcl.2010.04.081 BindingDB Entry DOI: 10.7270/Q21G0MF1 |
More data for this Ligand-Target Pair | |
Beta-secretase 1
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
KEGG
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| Article PubMed
| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Kinki University
Curated by ChEMBL
| Assay Description Inhibition of recombinant human BACE1 using Rh-EVNLDAEFK as substrate after 60 mins by fluorescence quenching assay |
Bioorg Med Chem 20: 784-8 (2012)
Article DOI: 10.1016/j.bmc.2011.12.002 BindingDB Entry DOI: 10.7270/Q2F47PKK |
More data for this Ligand-Target Pair | |
Sorbitol dehydrogenase
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB MMDB
KEGG
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Patents
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| Article PubMed
| n/a | n/a | 1.24E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Toyama
Curated by ChEMBL
| Assay Description Inhibition sorbitol dehydrogenase by spectrophotometric analysis |
Bioorg Med Chem Lett 20: 5630-3 (2010)
Article DOI: 10.1016/j.bmcl.2010.08.038 BindingDB Entry DOI: 10.7270/Q28052TK |
More data for this Ligand-Target Pair | |
Aldose reductase (AR)
(Homo sapiens (Human)) | BDBM50303499
(7-(methyloxy)-2H-chromen-2-one | 7-Methoxycoumarin...)Show InChI InChI=1S/C10H8O3/c1-12-8-4-2-7-3-5-10(11)13-9(7)6-8/h2-6H,1H3 | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
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| Article PubMed
| n/a | n/a | 1.31E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
King's College London
Curated by ChEMBL
| Assay Description Inhibition of human recombinant aldose reductase using D-glyceraldehyde as substrate preincubated for 10 mins before substrate addition measured for ... |
Bioorg Med Chem 20: 1251-8 (2012)
Article DOI: 10.1016/j.bmc.2011.12.033 BindingDB Entry DOI: 10.7270/Q2639Q5V |
More data for this Ligand-Target Pair | |