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SMILES: OC(=O)c1ccc(cc1)-c1cc(Cl)cc(Cl)c1

InChI Key: InChIKey=IFTKERBYCONAST-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50060972   

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
Regulatory protein E2 (Human papillomavirus type 16)	BDBM50060972 (3',5'-Dichloro-biphenyl-4-carboxylic acid | CHEMBL...) Show SMILES OC(=O)c1ccc(cc1)-c1cc(Cl)cc(Cl)c1 Show InChI InChI=1S/C13H8Cl2O2/c14-11-5-10(6-12(15)7-11)8-1-3-9(4-2-8)13(16)17/h1-7H,(H,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	6.00E+4	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Dissociation constant after binding to human papillomavirus E2 DNA-binding domain (DBD) by observing the changes in [15N]-HSQC spectra.				J Med Chem 40: 3144-50 (1997) Article DOI: 10.1021/jm9703404 BindingDB Entry DOI: 10.7270/Q2MG7NN2
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-gamma (Homo sapiens (Human))	BDBM50060972 (3',5'-Dichloro-biphenyl-4-carboxylic acid | CHEMBL...) Show SMILES OC(=O)c1ccc(cc1)-c1cc(Cl)cc(Cl)c1 Show InChI InChI=1S/C13H8Cl2O2/c14-11-5-10(6-12(15)7-11)8-1-3-9(4-2-8)13(16)17/h1-7H,(H,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a
Goethe-University Frankfurt Curated by ChEMBL					Assay Description Agonist activity at Gal4-LBD fused RXRgamma (unknown origin) expressed in HEK293T cells after 14 to 16 hrs by dual-Glo luciferase assay				ACS Med Chem Lett 10: 1346-1352 (2019) Article DOI: 10.1021/acsmedchemlett.9b00306 BindingDB Entry DOI: 10.7270/Q2TQ64T0
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50060972 (3',5'-Dichloro-biphenyl-4-carboxylic acid | CHEMBL...) Show SMILES OC(=O)c1ccc(cc1)-c1cc(Cl)cc(Cl)c1 Show InChI InChI=1S/C13H8Cl2O2/c14-11-5-10(6-12(15)7-11)8-1-3-9(4-2-8)13(16)17/h1-7H,(H,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	9.30E+3	n/a	n/a	n/a	n/a
Goethe-University Frankfurt Curated by ChEMBL					Assay Description Agonist activity at Gal4-LBD fused RXRalpha (unknown origin) expressed in HEK293T cells after 14 to 16 hrs by dual-Glo luciferase assay				ACS Med Chem Lett 10: 1346-1352 (2019) Article DOI: 10.1021/acsmedchemlett.9b00306 BindingDB Entry DOI: 10.7270/Q2TQ64T0
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-beta (Homo sapiens (Human))	BDBM50060972 (3',5'-Dichloro-biphenyl-4-carboxylic acid | CHEMBL...) Show SMILES OC(=O)c1ccc(cc1)-c1cc(Cl)cc(Cl)c1 Show InChI InChI=1S/C13H8Cl2O2/c14-11-5-10(6-12(15)7-11)8-1-3-9(4-2-8)13(16)17/h1-7H,(H,16,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a
Goethe-University Frankfurt Curated by ChEMBL					Assay Description Agonist activity at Gal4-LBD fused RXRbeta (unknown origin) expressed in HEK293T cells after 14 to 16 hrs by dual-Glo luciferase assay				ACS Med Chem Lett 10: 1346-1352 (2019) Article DOI: 10.1021/acsmedchemlett.9b00306 BindingDB Entry DOI: 10.7270/Q2TQ64T0
					More data for this Ligand-Target Pair