null

SMILES C\C(=C/c1ccc(cc1)C(O)=O)c1cc2c(cc1Cl)C(C)(C)CCC2(C)C

InChI Key InChIKey=ZMSVHSPBTBNKJJ-NTCAYCPXSA-N

  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 4 hits for monomerid = 50282693   

TargetRetinoic acid receptor RXR-alpha(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50282693(4-[(E)-2-(3-Chloro-5,5,8,8-tetramethyl-5,6,7,8-tet...)copy SMILEScopy InChI
Affinity DataEC50:  275nMAssay Description:Transcriptional activation for RXR alpha receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B8582K
TargetRetinoic acid receptor beta(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50282693(4-[(E)-2-(3-Chloro-5,5,8,8-tetramethyl-5,6,7,8-tet...)copy SMILEScopy InChI
Affinity DataEC50:  21nMAssay Description:Transcriptional activation for RAR beta receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B8582K
TargetRetinoic acid receptor alpha(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50282693(4-[(E)-2-(3-Chloro-5,5,8,8-tetramethyl-5,6,7,8-tet...)copy SMILEScopy InChI
Affinity DataEC50: >1.00E+3nMAssay Description:Transcriptional activation for RAR alpha receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B8582K
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50282693(4-[(E)-2-(3-Chloro-5,5,8,8-tetramethyl-5,6,7,8-tet...)copy SMILEScopy InChI
Affinity DataEC50:  77nMAssay Description:Transcriptional activation for RAR gamma receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B8582K