null

SMILES: NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1

InChI Key: InChIKey=MLNGSBPCBLCDLK-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50387162   

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 1 (Homo sapiens (Human))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	1.20	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
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2	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 9 (Homo sapiens (Human))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.60	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 12 (Homo sapiens (Human))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.90	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))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	5	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))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	12	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 9 (Homo sapiens (Human))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	12	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 2 (Homo sapiens (Human))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	421	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))	BDBM50387162 (4-ureidophenyl sulfamate ring derivative 3ba | CHE...) Show SMILES NS(=O)(=O)Oc1ccc(NC(=O)NCc2ccccn2)cc1 Show InChI InChI=1S/C13H14N4O4S/c14-22(19,20)21-12-6-4-10(5-7-12)17-13(18)16-9-11-3-1-2-8-15-11/h1-8H,9H2,(H2,14,19,20)(H2,16,17,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.01E+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