Compile Data Set for Download or QSAR

Found 3 hits of ki for monomerid = 50157952   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50157952 (2-Morpholin-4-yl-N-(5-sulfamoyl-[1,3,4]thiadiazol-...) Show SMILES NS(=O)(=O)c1nnc(NC(=O)CN2CCOCC2)s1 Show InChI InChI=1S/C8H13N5O4S2/c9-19(15,16)8-12-11-7(18-8)10-6(14)5-13-1-3-17-4-2-13/h1-5H2,(H2,9,15,16)(H,10,11,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Harran University Curated by ChEMBL					Assay Description Inhibitory potency against human cloned Carbonic anhydrase II expressed in Escherichia coli strain BL21				Bioorg Med Chem Lett 15: 367-72 (2004) Article DOI: 10.1016/j.bmcl.2004.10.070 BindingDB Entry DOI: 10.7270/Q2B858WB
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50157952 (2-Morpholin-4-yl-N-(5-sulfamoyl-[1,3,4]thiadiazol-...) Show SMILES NS(=O)(=O)c1nnc(NC(=O)CN2CCOCC2)s1 Show InChI InChI=1S/C8H13N5O4S2/c9-19(15,16)8-12-11-7(18-8)10-6(14)5-13-1-3-17-4-2-13/h1-5H2,(H2,9,15,16)(H,10,11,14)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	14	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Harran University Curated by ChEMBL					Assay Description Inhibitory potency against human cloned Carbonic anhydrase I expressed in Escherichia coli strain BL21				Bioorg Med Chem Lett 15: 367-72 (2004) Article DOI: 10.1016/j.bmcl.2004.10.070 BindingDB Entry DOI: 10.7270/Q2B858WB
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50157952 (2-Morpholin-4-yl-N-(5-sulfamoyl-[1,3,4]thiadiazol-...) Show SMILES NS(=O)(=O)c1nnc(NC(=O)CN2CCOCC2)s1 Show InChI InChI=1S/C8H13N5O4S2/c9-19(15,16)8-12-11-7(18-8)10-6(14)5-13-1-3-17-4-2-13/h1-5H2,(H2,9,15,16)(H,10,11,14)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	22	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Harran University Curated by ChEMBL					Assay Description Inhibitory potency against catalytic domain of human Carbonic anhydrase IX expressed in Escherichia coli strain BL21				Bioorg Med Chem Lett 15: 367-72 (2004) Article DOI: 10.1016/j.bmcl.2004.10.070 BindingDB Entry DOI: 10.7270/Q2B858WB
					More data for this Ligand-Target Pair