null

SMILES: CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O

InChI Key: InChIKey=NOYDKOIPFXMKRF-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50135774   

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
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	2.60E+3	n/a	n/a	n/a	n/a
Division of Eli Lilly & Company Curated by ChEMBL					Assay Description Cotransfection activity of compound against human Peroxisome proliferator activated receptor gamma was determined				J Med Chem 46: 5121-4 (2003) Article DOI: 10.1021/jm034173l BindingDB Entry DOI: 10.7270/Q2D50MB0
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	56	n/a	n/a	n/a	n/a
Division of Eli Lilly & Company Curated by ChEMBL					Assay Description Cotransfection activity against human Peroxisome proliferator activated receptor alpha				J Med Chem 46: 5121-4 (2003) Article DOI: 10.1021/jm034173l BindingDB Entry DOI: 10.7270/Q2D50MB0
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Division of Eli Lilly & Company Curated by ChEMBL					Assay Description Inhibitory activity of compound against the binding of human Peroxisome proliferator activated receptor gamma was determined				J Med Chem 46: 5121-4 (2003) Article DOI: 10.1021/jm034173l BindingDB Entry DOI: 10.7270/Q2D50MB0
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Division of Eli Lilly & Company Curated by ChEMBL					Assay Description Inhibitory activity against human Peroxisome proliferator activated receptor alpha				J Med Chem 46: 5121-4 (2003) Article DOI: 10.1021/jm034173l BindingDB Entry DOI: 10.7270/Q2D50MB0
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	879	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional Aut£noma de M£xico Curated by ChEMBL					Assay Description Agonist activity at PPARdelta				Bioorg Med Chem 20: 3523-32 (2012) Article DOI: 10.1016/j.bmc.2012.04.005 BindingDB Entry DOI: 10.7270/Q2MP54B4
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a
Division of Eli Lilly & Company Curated by ChEMBL					Assay Description Cotransfection activity of compound against human Peroxisome proliferator activated receptor delta was determined				J Med Chem 46: 5121-4 (2003) Article DOI: 10.1021/jm034173l BindingDB Entry DOI: 10.7270/Q2D50MB0
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor alpha (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional Aut£noma de M£xico Curated by ChEMBL					Assay Description Agonist activity at PPARalpha				Bioorg Med Chem 20: 3523-32 (2012) Article DOI: 10.1016/j.bmc.2012.04.005 BindingDB Entry DOI: 10.7270/Q2MP54B4
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor gamma (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional Aut£noma de M£xico Curated by ChEMBL					Assay Description Agonist activity at PPARgamma				Bioorg Med Chem 20: 3523-32 (2012) Article DOI: 10.1016/j.bmc.2012.04.005 BindingDB Entry DOI: 10.7270/Q2MP54B4
					More data for this Ligand-Target Pair
Peroxisome proliferator-activated receptor delta (Homo sapiens (Human))	BDBM50135774 (2-{4-[3-(1-Cyclohexylmethyl-5-oxo-4-propyl-4,5-dih...) Show SMILES CCCn1c(CCCc2ccc(OC(C)(C)C(O)=O)cc2)nn(CC2CCCCC2)c1=O Show InChI InChI=1S/C25H37N3O4/c1-4-17-27-22(26-28(24(27)31)18-20-9-6-5-7-10-20)12-8-11-19-13-15-21(16-14-19)32-25(2,3)23(29)30/h13-16,20H,4-12,17-18H2,1-3H3,(H,29,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	880	n/a	n/a	n/a	n/a	n/a	n/a
Division of Eli Lilly & Company Curated by ChEMBL					Assay Description Inhibitory activity of compound against the binding of human Peroxisome proliferator activated receptor delta was determined				J Med Chem 46: 5121-4 (2003) Article DOI: 10.1021/jm034173l BindingDB Entry DOI: 10.7270/Q2D50MB0
					More data for this Ligand-Target Pair