Found 4 hits for monomerid = 50190238 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 9
(Homo sapiens (Human)) | BDBM50190238
(2-(aminosulfonyl)-5-chloro-4-methylphenyl -N-(4-ni...)Show SMILES CCC(Sc1cc(Cl)c(C)cc1S(N)(=O)=O)=NNc1ccc(cc1)[N+]([O-])=O |w:16.17| Show InChI InChI=1S/C16H17ClN4O4S2/c1-3-16(20-19-11-4-6-12(7-5-11)21(22)23)26-14-9-13(17)10(2)8-15(14)27(18,24)25/h4-9,19H,3H2,1-2H3,(H2,18,24,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Medical University of Gdansk
Curated by ChEMBL
| Assay Description Inhibition of human cloned CA9 catalytic domain by CO2 hydration assay |
Bioorg Med Chem Lett 16: 4846-51 (2006)
Article DOI: 10.1016/j.bmcl.2006.06.064 BindingDB Entry DOI: 10.7270/Q2794493 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 2
(Homo sapiens (Human)) | BDBM50190238
(2-(aminosulfonyl)-5-chloro-4-methylphenyl -N-(4-ni...)Show SMILES CCC(Sc1cc(Cl)c(C)cc1S(N)(=O)=O)=NNc1ccc(cc1)[N+]([O-])=O |w:16.17| Show InChI InChI=1S/C16H17ClN4O4S2/c1-3-16(20-19-11-4-6-12(7-5-11)21(22)23)26-14-9-13(17)10(2)8-15(14)27(18,24)25/h4-9,19H,3H2,1-2H3,(H2,18,24,25) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Medical University of Gdansk
Curated by ChEMBL
| Assay Description Inhibition of human cloned CA2 by CO2 hydration assay |
Bioorg Med Chem Lett 16: 4846-51 (2006)
Article DOI: 10.1016/j.bmcl.2006.06.064 BindingDB Entry DOI: 10.7270/Q2794493 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 12
(Homo sapiens (Human)) | BDBM50190238
(2-(aminosulfonyl)-5-chloro-4-methylphenyl -N-(4-ni...)Show SMILES CCC(Sc1cc(Cl)c(C)cc1S(N)(=O)=O)=NNc1ccc(cc1)[N+]([O-])=O |w:16.17| Show InChI InChI=1S/C16H17ClN4O4S2/c1-3-16(20-19-11-4-6-12(7-5-11)21(22)23)26-14-9-13(17)10(2)8-15(14)27(18,24)25/h4-9,19H,3H2,1-2H3,(H2,18,24,25) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Medical University of Gdansk
Curated by ChEMBL
| Assay Description Inhibition of human cloned CA12 catalytic domain by CO2 hydration assay |
Bioorg Med Chem Lett 16: 4846-51 (2006)
Article DOI: 10.1016/j.bmcl.2006.06.064 BindingDB Entry DOI: 10.7270/Q2794493 |
More data for this Ligand-Target Pair | |
Carbonic anhydrase 1
(Homo sapiens (Human)) | BDBM50190238
(2-(aminosulfonyl)-5-chloro-4-methylphenyl -N-(4-ni...)Show SMILES CCC(Sc1cc(Cl)c(C)cc1S(N)(=O)=O)=NNc1ccc(cc1)[N+]([O-])=O |w:16.17| Show InChI InChI=1S/C16H17ClN4O4S2/c1-3-16(20-19-11-4-6-12(7-5-11)21(22)23)26-14-9-13(17)10(2)8-15(14)27(18,24)25/h4-9,19H,3H2,1-2H3,(H2,18,24,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 2.20E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Medical University of Gdansk
Curated by ChEMBL
| Assay Description Inhibition of human cloned CA1 by CO2 hydration assay |
Bioorg Med Chem Lett 16: 4846-51 (2006)
Article DOI: 10.1016/j.bmcl.2006.06.064 BindingDB Entry DOI: 10.7270/Q2794493 |
More data for this Ligand-Target Pair | |