BDBM50349845 CHEMBL1813207

SMILES: COC(=O)CNc1nc(NCC(=O)OC)nc(Nc2ccc(cc2)S(N)(=O)=O)n1

InChI Key: InChIKey=AXBFLIXVCSHIIF-UHFFFAOYSA-N

Data: 5 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 5 hits for monomerid = 50349845   

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 XIV (Homo sapiens (Human))	BDBM50349845 (CHEMBL1813207) Show SMILES COC(=O)CNc1nc(NCC(=O)OC)nc(Nc2ccc(cc2)S(N)(=O)=O)n1 Show InChI InChI=1S/C15H19N7O6S/c1-27-11(23)7-17-13-20-14(18-8-12(24)28-2)22-15(21-13)19-9-3-5-10(6-4-9)29(16,25)26/h3-6H,7-8H2,1-2H3,(H2,16,25,26)(H3,17,18,19,20,21,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibition of human recombinant carbonic anhydrase 14 preincubated for 15 mins by CO2 hydration method				Bioorg Med Chem 19: 3105-19 (2011) Article DOI: 10.1016/j.bmc.2011.04.005 BindingDB Entry DOI: 10.7270/Q2FF3SQ6
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50349845 (CHEMBL1813207) Show SMILES COC(=O)CNc1nc(NCC(=O)OC)nc(Nc2ccc(cc2)S(N)(=O)=O)n1 Show InChI InChI=1S/C15H19N7O6S/c1-27-11(23)7-17-13-20-14(18-8-12(24)28-2)22-15(21-13)19-9-3-5-10(6-4-9)29(16,25)26/h3-6H,7-8H2,1-2H3,(H2,16,25,26)(H3,17,18,19,20,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibition of human recombinant carbonic anhydrase 12 preincubated for 15 mins by CO2 hydration method				Bioorg Med Chem 19: 3105-19 (2011) Article DOI: 10.1016/j.bmc.2011.04.005 BindingDB Entry DOI: 10.7270/Q2FF3SQ6
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50349845 (CHEMBL1813207) Show SMILES COC(=O)CNc1nc(NCC(=O)OC)nc(Nc2ccc(cc2)S(N)(=O)=O)n1 Show InChI InChI=1S/C15H19N7O6S/c1-27-11(23)7-17-13-20-14(18-8-12(24)28-2)22-15(21-13)19-9-3-5-10(6-4-9)29(16,25)26/h3-6H,7-8H2,1-2H3,(H2,16,25,26)(H3,17,18,19,20,21,22)	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	9.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibition of human recombinant carbonic anhydrase 9 preincubated for 15 mins by CO2 hydration method				Bioorg Med Chem 19: 3105-19 (2011) Article DOI: 10.1016/j.bmc.2011.04.005 BindingDB Entry DOI: 10.7270/Q2FF3SQ6
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50349845 (CHEMBL1813207) Show SMILES COC(=O)CNc1nc(NCC(=O)OC)nc(Nc2ccc(cc2)S(N)(=O)=O)n1 Show InChI InChI=1S/C15H19N7O6S/c1-27-11(23)7-17-13-20-14(18-8-12(24)28-2)22-15(21-13)19-9-3-5-10(6-4-9)29(16,25)26/h3-6H,7-8H2,1-2H3,(H2,16,25,26)(H3,17,18,19,20,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	435	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibition of human recombinant cytosolic carbonic anhydrase 2 preincubated for 15 mins by CO2 hydration method				Bioorg Med Chem 19: 3105-19 (2011) Article DOI: 10.1016/j.bmc.2011.04.005 BindingDB Entry DOI: 10.7270/Q2FF3SQ6
					More data for this Ligand-Target Pair				3D Structure (docked)
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50349845 (CHEMBL1813207) Show SMILES COC(=O)CNc1nc(NCC(=O)OC)nc(Nc2ccc(cc2)S(N)(=O)=O)n1 Show InChI InChI=1S/C15H19N7O6S/c1-27-11(23)7-17-13-20-14(18-8-12(24)28-2)22-15(21-13)19-9-3-5-10(6-4-9)29(16,25)26/h3-6H,7-8H2,1-2H3,(H2,16,25,26)(H3,17,18,19,20,21,22)	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	502	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibition of human recombinant cytosolic carbonic anhydrase 1 preincubated for 15 mins by CO2 hydration method				Bioorg Med Chem 19: 3105-19 (2011) Article DOI: 10.1016/j.bmc.2011.04.005 BindingDB Entry DOI: 10.7270/Q2FF3SQ6
					More data for this Ligand-Target Pair