BDBM50330334 CHEMBL1276024::Ethyl1-(2-methyl-1-(2-oxopropyl)-1H-indol-4-yl)-5-phenyl-3-(5-sulfamoyl-1,3,4-thiadiazol-2-ylcarbamoyl)-1Hpyrazole-4-carboxylate

SMILES: CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc2n(CC(C)=O)c(C)cc12)C(=O)Nc1nnc(s1)S(N)(=O)=O

InChI Key: InChIKey=SXHIGFDZDJWQOJ-UHFFFAOYSA-N

Data: 2 KI  4 IC50

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 6 hits for monomerid = 50330334   

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))	BDBM50330334 (CHEMBL1276024 | Ethyl1-(2-methyl-1-(2-oxopropyl)-1...) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc2n(CC(C)=O)c(C)cc12)C(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C27H25N7O6S2/c1-4-40-25(37)21-22(24(36)29-26-30-31-27(41-26)42(28,38)39)32-34(23(21)17-9-6-5-7-10-17)20-12-8-11-19-18(20)13-15(2)33(19)14-16(3)35/h5-13H,4,14H2,1-3H3,(H2,28,38,39)(H,29,30,36)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 2 by Lineweaver-Burk plot analysis				Eur J Med Chem 45: 4769-73 (2010) Article DOI: 10.1016/j.ejmech.2010.07.041 BindingDB Entry DOI: 10.7270/Q2X06796
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50330334 (CHEMBL1276024 | Ethyl1-(2-methyl-1-(2-oxopropyl)-1...) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc2n(CC(C)=O)c(C)cc12)C(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C27H25N7O6S2/c1-4-40-25(37)21-22(24(36)29-26-30-31-27(41-26)42(28,38)39)32-34(23(21)17-9-6-5-7-10-17)20-12-8-11-19-18(20)13-15(2)33(19)14-16(3)35/h5-13H,4,14H2,1-3H3,(H2,28,38,39)(H,29,30,36)	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	380	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 1 by Lineweaver-Burk plot analysis				Eur J Med Chem 45: 4769-73 (2010) Article DOI: 10.1016/j.ejmech.2010.07.041 BindingDB Entry DOI: 10.7270/Q2X06796
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50330334 (CHEMBL1276024 | Ethyl1-(2-methyl-1-(2-oxopropyl)-1...) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc2n(CC(C)=O)c(C)cc12)C(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C27H25N7O6S2/c1-4-40-25(37)21-22(24(36)29-26-30-31-27(41-26)42(28,38)39)32-34(23(21)17-9-6-5-7-10-17)20-12-8-11-19-18(20)13-15(2)33(19)14-16(3)35/h5-13H,4,14H2,1-3H3,(H2,28,38,39)(H,29,30,36)	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	n/a	n/a	70	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 1 esterase activity by spectrophotometry				Eur J Med Chem 45: 4769-73 (2010) Article DOI: 10.1016/j.ejmech.2010.07.041 BindingDB Entry DOI: 10.7270/Q2X06796
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50330334 (CHEMBL1276024 | Ethyl1-(2-methyl-1-(2-oxopropyl)-1...) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc2n(CC(C)=O)c(C)cc12)C(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C27H25N7O6S2/c1-4-40-25(37)21-22(24(36)29-26-30-31-27(41-26)42(28,38)39)32-34(23(21)17-9-6-5-7-10-17)20-12-8-11-19-18(20)13-15(2)33(19)14-16(3)35/h5-13H,4,14H2,1-3H3,(H2,28,38,39)(H,29,30,36)	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	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 1 hydratase activity by spectrophotometry				Eur J Med Chem 45: 4769-73 (2010) Article DOI: 10.1016/j.ejmech.2010.07.041 BindingDB Entry DOI: 10.7270/Q2X06796
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50330334 (CHEMBL1276024 | Ethyl1-(2-methyl-1-(2-oxopropyl)-1...) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc2n(CC(C)=O)c(C)cc12)C(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C27H25N7O6S2/c1-4-40-25(37)21-22(24(36)29-26-30-31-27(41-26)42(28,38)39)32-34(23(21)17-9-6-5-7-10-17)20-12-8-11-19-18(20)13-15(2)33(19)14-16(3)35/h5-13H,4,14H2,1-3H3,(H2,28,38,39)(H,29,30,36)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 2 esterase activity by spectrophotometry				Eur J Med Chem 45: 4769-73 (2010) Article DOI: 10.1016/j.ejmech.2010.07.041 BindingDB Entry DOI: 10.7270/Q2X06796
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50330334 (CHEMBL1276024 | Ethyl1-(2-methyl-1-(2-oxopropyl)-1...) Show SMILES CCOC(=O)c1c(nn(c1-c1ccccc1)-c1cccc2n(CC(C)=O)c(C)cc12)C(=O)Nc1nnc(s1)S(N)(=O)=O Show InChI InChI=1S/C27H25N7O6S2/c1-4-40-25(37)21-22(24(36)29-26-30-31-27(41-26)42(28,38)39)32-34(23(21)17-9-6-5-7-10-17)20-12-8-11-19-18(20)13-15(2)33(19)14-16(3)35/h5-13H,4,14H2,1-3H3,(H2,28,38,39)(H,29,30,36)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	240	n/a	n/a	n/a	n/a	n/a	n/a
Dumlupinar University Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase 2 hydratase activity by spectrophotometry				Eur J Med Chem 45: 4769-73 (2010) Article DOI: 10.1016/j.ejmech.2010.07.041 BindingDB Entry DOI: 10.7270/Q2X06796
					More data for this Ligand-Target Pair