null

SMILES: Cc1ccc(cc1)S(=O)(=O)Nc1cc(C)ccc1[Se][Se]c1ccc(C)cc1NS(=O)(=O)c1ccc(C)cc1

InChI Key: InChIKey=PQLDISKCBJFIRV-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50248564   

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))	BDBM50248564 (CHEMBL4069637) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1cc(C)ccc1[Se][Se]c1ccc(C)cc1NS(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C28H28N2O4S2Se2/c1-19-5-11-23(12-6-19)35(31,32)29-25-17-21(3)9-15-27(25)37-38-28-16-10-22(4)18-26(28)30-36(33,34)24-13-7-20(2)8-14-24/h5-18,29-30H,1-4H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	1.60E+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 recombinant human transmembrane carbonic anhydrase 9 pretreated for 15 mins prior to testing measured for 10 to 100 secs by phenol red ...				Bioorg Med Chem 25: 2518-2523 (2017) Article DOI: 10.1016/j.bmc.2017.03.013 BindingDB Entry DOI: 10.7270/Q25B04XC
					More data for this Ligand-Target Pair
Carbonic anhydrase 7 (Homo sapiens (Human))	BDBM50248564 (CHEMBL4069637) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1cc(C)ccc1[Se][Se]c1ccc(C)cc1NS(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C28H28N2O4S2Se2/c1-19-5-11-23(12-6-19)35(31,32)29-25-17-21(3)9-15-27(25)37-38-28-16-10-22(4)18-26(28)30-36(33,34)24-13-7-20(2)8-14-24/h5-18,29-30H,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	5.80E+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 recombinant human cytosolic carbonic anhydrase 7 pretreated for 15 mins prior to testing measured for 10 to 100 secs by phenol red base...				Bioorg Med Chem 25: 2518-2523 (2017) Article DOI: 10.1016/j.bmc.2017.03.013 BindingDB Entry DOI: 10.7270/Q25B04XC
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50248564 (CHEMBL4069637) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1cc(C)ccc1[Se][Se]c1ccc(C)cc1NS(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C28H28N2O4S2Se2/c1-19-5-11-23(12-6-19)35(31,32)29-25-17-21(3)9-15-27(25)37-38-28-16-10-22(4)18-26(28)30-36(33,34)24-13-7-20(2)8-14-24/h5-18,29-30H,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	3.09E+4	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 recombinant human cytosolic carbonic anhydrase 2 pretreated for 15 mins prior to testing measured for 10 to 100 secs by phenol red base...				Bioorg Med Chem 25: 2518-2523 (2017) Article DOI: 10.1016/j.bmc.2017.03.013 BindingDB Entry DOI: 10.7270/Q25B04XC
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Homo sapiens (Human))	BDBM50248564 (CHEMBL4069637) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1cc(C)ccc1[Se][Se]c1ccc(C)cc1NS(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C28H28N2O4S2Se2/c1-19-5-11-23(12-6-19)35(31,32)29-25-17-21(3)9-15-27(25)37-38-28-16-10-22(4)18-26(28)30-36(33,34)24-13-7-20(2)8-14-24/h5-18,29-30H,1-4H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	7.89E+4	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 recombinant human membrane bound carbonic anhydrase 4 pretreated for 15 mins prior to testing measured for 10 to 100 secs by phenol red...				Bioorg Med Chem 25: 2518-2523 (2017) Article DOI: 10.1016/j.bmc.2017.03.013 BindingDB Entry DOI: 10.7270/Q25B04XC
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50248564 (CHEMBL4069637) Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1cc(C)ccc1[Se][Se]c1ccc(C)cc1NS(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C28H28N2O4S2Se2/c1-19-5-11-23(12-6-19)35(31,32)29-25-17-21(3)9-15-27(25)37-38-28-16-10-22(4)18-26(28)30-36(33,34)24-13-7-20(2)8-14-24/h5-18,29-30H,1-4H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	8.13E+4	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 recombinant human cytosolic carbonic anhydrase 1 pretreated for 15 mins prior to testing measured for 10 to 100 secs by phenol red base...				Bioorg Med Chem 25: 2518-2523 (2017) Article DOI: 10.1016/j.bmc.2017.03.013 BindingDB Entry DOI: 10.7270/Q25B04XC
					More data for this Ligand-Target Pair