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SMILES: CC(C)c1cccc(c1)[C@H](C)NC(=O)c1ccc2n(Cc3cccc(O[C@H](C)C(O)=O)c3)c(C)c(C)c2c1

InChI Key: InChIKey=HJSFJKFQTHNUFG-JTHBVZDNSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 161134   
Target/Host
(Institution)		LigandTarget/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		pHTemp
°C
Peroxisome proliferator-activated receptor gamma


(Homo sapiens (Human))		BDBM161134
PNG
(US9051265, 42)
Show SMILES CC(C)c1cccc(c1)[C@H](C)NC(=O)c1ccc2n(Cc3cccc(O[C@H](C)C(O)=O)c3)c(C)c(C)c2c1 |r|
Show InChI InChI=1S/C32H36N2O4/c1-19(2)25-10-8-11-26(16-25)21(4)33-31(35)27-13-14-30-29(17-27)20(3)22(5)34(30)18-24-9-7-12-28(15-24)38-23(6)32(36)37/h7-17,19,21,23H,18H2,1-6H3,(H,33,35)(H,36,37)/t21-,23+/m0/s1
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Similars
US Patent
n/an/a 550n/an/an/an/an/an/a



The Scripps Research Institute

US Patent


Assay Description
The assay was performed according to manufacturer protocol. A mixture of 5 nM GST-PPARG-LBD, 5 nM Tb-GST-antibody, 5 nM Fluormone Pan- PPAR Green, an...

US Patent US9051265 (2015)


BindingDB Entry DOI: 10.7270/Q2FT8JSW
More data for this
Ligand-Target Pair