BDBM50523348 CHEMBL4519564

SMILES: COc1ccc(cc1)C1=NN(C(=O)CC1)c1ccc(cc1)S(N)(=O)=O

InChI Key: InChIKey=ODCSKQOYUFEELP-UHFFFAOYSA-N

Data: 4 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50523348   

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 2 (Homo sapiens (Human))	BDBM50523348 (CHEMBL4519564) Show SMILES COc1ccc(cc1)C1=NN(C(=O)CC1)c1ccc(cc1)S(N)(=O)=O |t:9| Show InChI InChI=1S/C17H17N3O4S/c1-24-14-6-2-12(3-7-14)16-10-11-17(21)20(19-16)13-4-8-15(9-5-13)25(18,22)23/h2-9H,10-11H2,1H3,(H2,18,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.0800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Saint Petersburg State University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA 2 preincubated for 15 mins by phenol red dye-based stopped-flow CO2 hydration assay				Eur J Med Chem 168: 301-314 (2019) Article DOI: 10.1016/j.ejmech.2019.02.044
					More data for this Ligand-Target Pair
Carbonic anhydrases; II & IX (Homo sapiens (Human))	BDBM50523348 (CHEMBL4519564) Show SMILES COc1ccc(cc1)C1=NN(C(=O)CC1)c1ccc(cc1)S(N)(=O)=O |t:9| Show InChI InChI=1S/C17H17N3O4S/c1-24-14-6-2-12(3-7-14)16-10-11-17(21)20(19-16)13-4-8-15(9-5-13)25(18,22)23/h2-9H,10-11H2,1H3,(H2,18,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Saint Petersburg State University Curated by ChEMBL					Assay Description Inhibition of membrane bound human CA 9 preincubated for 15 mins by phenol red dye-based stopped-flow CO2 hydration assay				Eur J Med Chem 168: 301-314 (2019) Article DOI: 10.1016/j.ejmech.2019.02.044
					More data for this Ligand-Target Pair
Carbonic anhydrase (Homo sapiens (Human))	BDBM50523348 (CHEMBL4519564) Show SMILES COc1ccc(cc1)C1=NN(C(=O)CC1)c1ccc(cc1)S(N)(=O)=O |t:9| Show InChI InChI=1S/C17H17N3O4S/c1-24-14-6-2-12(3-7-14)16-10-11-17(21)20(19-16)13-4-8-15(9-5-13)25(18,22)23/h2-9H,10-11H2,1H3,(H2,18,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	9.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Saint Petersburg State University Curated by ChEMBL					Assay Description Inhibition of membrane bound human CA 12 preincubated for 15 mins by phenol red dye-based stopped-flow CO2 hydration assay				Eur J Med Chem 168: 301-314 (2019) Article DOI: 10.1016/j.ejmech.2019.02.044
					More data for this Ligand-Target Pair
Carbonic anhydrase (Homo sapiens (Human))	BDBM50523348 (CHEMBL4519564) Show SMILES COc1ccc(cc1)C1=NN(C(=O)CC1)c1ccc(cc1)S(N)(=O)=O |t:9| Show InChI InChI=1S/C17H17N3O4S/c1-24-14-6-2-12(3-7-14)16-10-11-17(21)20(19-16)13-4-8-15(9-5-13)25(18,22)23/h2-9H,10-11H2,1H3,(H2,18,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	93	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Saint Petersburg State University Curated by ChEMBL					Assay Description Inhibition of human cytosolic CA 1 preincubated for 15 mins by phenol red dye-based stopped-flow CO2 hydration assay				Eur J Med Chem 168: 301-314 (2019) Article DOI: 10.1016/j.ejmech.2019.02.044
					More data for this Ligand-Target Pair