BDBM50345222 2-ethyl-N-(4-sulfamoylphenyl)pentanamide::CHEMBL1084063

SMILES: CCCC(CC)C(=O)Nc1ccc(cc1)S(N)(=O)=O

InChI Key: InChIKey=HAACFJPQNWDJLD-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 = 50345222   

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))	BDBM50345222 (2-ethyl-N-(4-sulfamoylphenyl)pentanamide | CHEMBL1...) Show SMILES CCCC(CC)C(=O)Nc1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C13H20N2O3S/c1-3-5-10(4-2)13(16)15-11-6-8-12(9-7-11)19(14,17)18/h6-10H,3-5H2,1-2H3,(H,15,16)(H2,14,17,18)	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Hebrew University of Jerusalem Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 14 preincubated with compound for 15 mins by carbon dioxide hydration assay				J Med Chem 54: 3977-81 (2011) Article DOI: 10.1021/jm200209n BindingDB Entry DOI: 10.7270/Q2736R8S
					More data for this Ligand-Target Pair
Carbonic anhydrase 7 (Homo sapiens (Human))	BDBM50345222 (2-ethyl-N-(4-sulfamoylphenyl)pentanamide | CHEMBL1...) Show SMILES CCCC(CC)C(=O)Nc1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C13H20N2O3S/c1-3-5-10(4-2)13(16)15-11-6-8-12(9-7-11)19(14,17)18/h6-10H,3-5H2,1-2H3,(H,15,16)(H2,14,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Hebrew University of Jerusalem Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 7 preincubated with compound for 15 mins by carbon dioxide hydration assay				J Med Chem 54: 3977-81 (2011) Article DOI: 10.1021/jm200209n BindingDB Entry DOI: 10.7270/Q2736R8S
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50345222 (2-ethyl-N-(4-sulfamoylphenyl)pentanamide | CHEMBL1...) Show SMILES CCCC(CC)C(=O)Nc1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C13H20N2O3S/c1-3-5-10(4-2)13(16)15-11-6-8-12(9-7-11)19(14,17)18/h6-10H,3-5H2,1-2H3,(H,15,16)(H2,14,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	321	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Hebrew University of Jerusalem Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 2 preincubated with compound for 15 mins by carbon dioxide hydration assay				J Med Chem 54: 3977-81 (2011) Article DOI: 10.1021/jm200209n BindingDB Entry DOI: 10.7270/Q2736R8S
					More data for this Ligand-Target Pair				3D Structure (docked)
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50345222 (2-ethyl-N-(4-sulfamoylphenyl)pentanamide | CHEMBL1...) Show SMILES CCCC(CC)C(=O)Nc1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C13H20N2O3S/c1-3-5-10(4-2)13(16)15-11-6-8-12(9-7-11)19(14,17)18/h6-10H,3-5H2,1-2H3,(H,15,16)(H2,14,17,18)	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	1.56E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Hebrew University of Jerusalem Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 1 preincubated with compound for 15 mins by carbon dioxide hydration assay				J Med Chem 54: 3977-81 (2011) Article DOI: 10.1021/jm200209n BindingDB Entry DOI: 10.7270/Q2736R8S
					More data for this Ligand-Target Pair