BDBM50361286 CHEMBL1935611

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

InChI Key InChIKey=XGFUSEMJOOJECK-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 = 50361286   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Kyoto Pharmaceutical Industries

Curated by ChEMBL
LigandPNGBDBM50361286(CHEMBL1935611)
Affinity DataIC50: 940nMAssay 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
TargetPeroxisome proliferator-activated receptor gamma(Human)
Kyoto Pharmaceutical Industries

Curated by ChEMBL
LigandPNGBDBM50361286(CHEMBL1935611)
Affinity DataEC50:  20nMAssay 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