BDBM50361298 CHEMBL1935496

SMILES CCC(C)(C)\C=C\c1nc(CCOc2ccc3C[C@H](N(Cc3c2)C(=O)\C=C\C=C\C)C(O)=O)c(C)o1

InChI Key InChIKey=KBTJRXUWHKVRNI-UHFFFAOYSA-N

Data  1 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50361298   

TargetPeroxisome proliferator-activated receptor gamma(Human)
Kyoto Pharmaceutical Industries

Curated by ChEMBL
LigandPNGBDBM50361298(CHEMBL1935496)
Affinity DataEC50:  760nMAssay Description:Transactivation of human full length PPARgamma expressed in COS1 cells co-transfected with RXRalpha after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Kyoto Pharmaceutical Industries

Curated by ChEMBL
LigandPNGBDBM50361298(CHEMBL1935496)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of PTB1B using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed