Compile Data Set for Download or QSAR

Found 9 hits of ki for monomerid = 50387160   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-12				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 12 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay				Bioorg Med Chem Lett 22: 4681-5 (2012) Article DOI: 10.1016/j.bmcl.2012.05.083 BindingDB Entry DOI: 10.7270/Q20866C2
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology									J Enzyme Inhib Med Chem 29: 571-81 (2014) Article DOI: 10.3109/14756366.2013.827677 BindingDB Entry DOI: 10.7270/Q2NC5ZCQ
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-9				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 9 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay				Bioorg Med Chem Lett 22: 4681-5 (2012) Article DOI: 10.1016/j.bmcl.2012.05.083 BindingDB Entry DOI: 10.7270/Q20866C2
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	216	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-2				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	236	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 2 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay				Bioorg Med Chem Lett 22: 4681-5 (2012) Article DOI: 10.1016/j.bmcl.2012.05.083 BindingDB Entry DOI: 10.7270/Q20866C2
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ecole Nationale Sup£rieure de Chimie de Montpellier Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 1 preincubated for 15 mins measured for 10 to 100 sec using phenol red indicator-based stopped flow assay				Bioorg Med Chem Lett 22: 4681-5 (2012) Article DOI: 10.1016/j.bmcl.2012.05.083 BindingDB Entry DOI: 10.7270/Q20866C2
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50387160 (4-ureidophenyl sulfamate ring derivative 3ay | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCCc2cccs2)cc1 Show InChI InChI=1S/C13H15N3O4S2/c14-22(18,19)20-11-5-3-10(4-6-11)16-13(17)15-8-7-12-2-1-9-21-12/h1-6,9H,7-8H2,(H2,14,18,19)(H2,15,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-1				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair