BDBM33274 azo-sulfonamide, 2d

SMILES: CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O

InChI Key: InChIKey=AZWGZSIGPVBVHJ-WUKNDPDISA-N

Data: 7 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 7 hits for monomerid = 33274   

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 9 (Homo sapiens (Human))	BDBM33274 (azo-sulfonamide, 2d) Show SMILES CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-8-6-11(7-9-13)16-17-12-4-3-5-14(10-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	6.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Firenze					Assay Description An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...				Bioorg Med Chem 17: 7093-9 (2009) Article DOI: 10.1016/j.bmc.2009.09.003 BindingDB Entry DOI: 10.7270/Q2M32T4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM33274 (azo-sulfonamide, 2d) Show SMILES CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-8-6-11(7-9-13)16-17-12-4-3-5-14(10-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	7.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Firenze					Assay Description An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...				Bioorg Med Chem 17: 7093-9 (2009) Article DOI: 10.1016/j.bmc.2009.09.003 BindingDB Entry DOI: 10.7270/Q2M32T4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM33274 (azo-sulfonamide, 2d) Show SMILES CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-8-6-11(7-9-13)16-17-12-4-3-5-14(10-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	105	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 cloned full length carbonic anhydrase 2 by stopped flow CO2 hydration assay				Bioorg Med Chem Lett 19: 4929-32 (2009) Article DOI: 10.1016/j.bmcl.2009.07.088 BindingDB Entry DOI: 10.7270/Q2H70GSS
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM33274 (azo-sulfonamide, 2d) Show SMILES CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-8-6-11(7-9-13)16-17-12-4-3-5-14(10-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	105	-9.51	n/a	n/a	n/a	n/a	n/a	7.4	25
Universita degli Studi di Firenze					Assay Description An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...				Bioorg Med Chem 17: 7093-9 (2009) Article DOI: 10.1016/j.bmc.2009.09.003 BindingDB Entry DOI: 10.7270/Q2M32T4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM33274 (azo-sulfonamide, 2d) Show SMILES CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-8-6-11(7-9-13)16-17-12-4-3-5-14(10-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	113	-9.47	n/a	n/a	n/a	n/a	n/a	7.4	25
Universita degli Studi di Firenze					Assay Description An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...				Bioorg Med Chem 17: 7093-9 (2009) Article DOI: 10.1016/j.bmc.2009.09.003 BindingDB Entry DOI: 10.7270/Q2M32T4Q
					More data for this Ligand-Target Pair
Carbonic Anhydrase (mtCA 1) (Mycobacterium tuberculosis)	BDBM33274 (azo-sulfonamide, 2d) Show SMILES CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-8-6-11(7-9-13)16-17-12-4-3-5-14(10-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	7.54E+3	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 Mycobacterium tuberculosis recombinant carbonic anhydrase Rv1284 by stopped flow CO2 hydration assay				Bioorg Med Chem Lett 19: 4929-32 (2009) Article DOI: 10.1016/j.bmcl.2009.07.088 BindingDB Entry DOI: 10.7270/Q2H70GSS
					More data for this Ligand-Target Pair
PROBABLE TRANSMEMBRANE CARBONIC ANHYDRASE (CARBONATE DEHYDRATASE) (CARBONIC DEHYDRATASE) (Mycobacterium tuberculosis)	BDBM33274 (azo-sulfonamide, 2d) Show SMILES CN(C)c1ccc(cc1)\N=N\c1cccc(c1)S(N)(=O)=O Show InChI InChI=1S/C14H16N4O2S/c1-18(2)13-8-6-11(7-9-13)16-17-12-4-3-5-14(10-12)21(15,19)20/h3-10H,1-2H3,(H2,15,19,20)/b17-16+	KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	9.36E+3	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 Mycobacterium tuberculosis recombinant carbonic anhydrase Rv3273 by stopped flow CO2 hydration assay				Bioorg Med Chem Lett 19: 4929-32 (2009) Article DOI: 10.1016/j.bmcl.2009.07.088 BindingDB Entry DOI: 10.7270/Q2H70GSS
					More data for this Ligand-Target Pair