BDBM50361299 CHEMBL1935494

SMILES C\C=C\C=C\C(=O)N1Cc2cc(OCCc3nc(\C=C\C(C)(C)C)oc3C)ccc2C[C@H]1C(O)=O

InChI Key InChIKey=YGDZMPWWLQYQQR-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 = 50361299   

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

Curated by ChEMBL
LigandPNGBDBM50361299(CHEMBL1935494)
Affinity DataEC50:  540nMAssay 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
LigandPNGBDBM50361299(CHEMBL1935494)
Affinity DataIC50: 2.25E+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