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SMILES: COc1cccc2OC(C(C)C)c3c(ccc4NC(C)(C)C=C(C)c34)-c12

InChI Key: InChIKey=LONLTTQFSBAAKV-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50107364   

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
Glucocorticoid receptor (Homo sapiens (Human))	BDBM50107364 (5-Isopropyl-10-methoxy-2,2,4-trimethyl-2,5-dihydro...) Show SMILES COc1cccc2OC(C(C)C)c3c(ccc4NC(C)(C)C=C(C)c34)-c12 |t:21| Show InChI InChI=1S/C23H27NO2/c1-13(2)22-21-15(20-17(25-6)8-7-9-18(20)26-22)10-11-16-19(21)14(3)12-23(4,5)24-16/h7-13,22,24H,1-6H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity towards glucocorticoid receptor (GR) by displacing [3H]-Dexamethasone				J Med Chem 44: 4481-91 (2001) BindingDB Entry DOI: 10.7270/Q2CZ36F4
					More data for this Ligand-Target Pair
Progesterone receptor (Homo sapiens (Human))	BDBM50107364 (5-Isopropyl-10-methoxy-2,2,4-trimethyl-2,5-dihydro...) Show SMILES COc1cccc2OC(C(C)C)c3c(ccc4NC(C)(C)C=C(C)c34)-c12 |t:21| Show InChI InChI=1S/C23H27NO2/c1-13(2)22-21-15(20-17(25-6)8-7-9-18(20)26-22)10-11-16-19(21)14(3)12-23(4,5)24-16/h7-13,22,24H,1-6H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity towards progesterone receptor (PR) by displacing [3H]-progesterone.				J Med Chem 44: 4481-91 (2001) BindingDB Entry DOI: 10.7270/Q2CZ36F4
					More data for this Ligand-Target Pair
Glucocorticoid receptor (Homo sapiens (Human))	BDBM50107364 (5-Isopropyl-10-methoxy-2,2,4-trimethyl-2,5-dihydro...) Show SMILES COc1cccc2OC(C(C)C)c3c(ccc4NC(C)(C)C=C(C)c34)-c12 |t:21| Show InChI InChI=1S/C23H27NO2/c1-13(2)22-21-15(20-17(25-6)8-7-9-18(20)26-22)10-11-16-19(21)14(3)12-23(4,5)24-16/h7-13,22,24H,1-6H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	146	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description The effective concentration in CV-1 cells for glucocorticoid response element activation (GRE).				J Med Chem 44: 4481-91 (2001) BindingDB Entry DOI: 10.7270/Q2CZ36F4
					More data for this Ligand-Target Pair
Glucocorticoid receptor (Homo sapiens (Human))	BDBM50107364 (5-Isopropyl-10-methoxy-2,2,4-trimethyl-2,5-dihydro...) Show SMILES COc1cccc2OC(C(C)C)c3c(ccc4NC(C)(C)C=C(C)c34)-c12 |t:21| Show InChI InChI=1S/C23H27NO2/c1-13(2)22-21-15(20-17(25-6)8-7-9-18(20)26-22)10-11-16-19(21)14(3)12-23(4,5)24-16/h7-13,22,24H,1-6H3	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	39	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Effective concentration in HepG2 cells transfected with LUC gene (E-sel-Luc).				J Med Chem 44: 4481-91 (2001) BindingDB Entry DOI: 10.7270/Q2CZ36F4
					More data for this Ligand-Target Pair