null

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

InChI Key InChIKey=BOODRZWPUUYTES-GHIVURASSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50361295   

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

Curated by ChEMBL
LigandPNGBDBM50361295(CHEMBL1935499)copy SMILEScopy InChI
Affinity DataIC50: 1.18E+3nMAssay Description:Inhibition of PTB1B using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZZSPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Kyoto Pharmaceutical Industries

Curated by ChEMBL
LigandPNGBDBM50361295(CHEMBL1935499)copy SMILEScopy InChI
Affinity DataEC50:  30nMAssay 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 DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZZSPubMed