BDBM25864 3-[4-(4-hydroxyphenyl)phenyl]phenol::hydroxyphenyl substituted benzene, 36

SMILES Oc1ccc(cc1)-c1ccc(cc1)-c1cccc(O)c1

InChI Key InChIKey=RPJZTMNVHGSNCA-UHFFFAOYSA-N

Data  4 IC50

  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 = 25864   

Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Saarland University

LigandPNGBDBM25864(3-[4-(4-hydroxyphenyl)phenyl]phenol | hydroxypheny...)
Affinity DataIC50:  471nMAssay Description:Tritiated E1 was incubated with 17beta-HSD1, cofactor, and inhibitor. The amount of labeled E2 formed was quantified by HPLC. Detection and quantific...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Saarland University

Curated by ChEMBL
LigandPNGBDBM25864(3-[4-(4-hydroxyphenyl)phenyl]phenol | hydroxypheny...)
Affinity DataIC50:  4.51E+3nMAssay Description:Inhibition of human placental 17betaHSD2 by radiodetection assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 1(Homo sapiens (Human))
Saarland University

LigandPNGBDBM25864(3-[4-(4-hydroxyphenyl)phenyl]phenol | hydroxypheny...)
Affinity DataIC50:  471nMAssay Description:Inhibition of human placental 17betaHSD1 by radiodetection assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 2(Homo sapiens (Human))
Saarland University

Curated by ChEMBL
LigandPNGBDBM25864(3-[4-(4-hydroxyphenyl)phenyl]phenol | hydroxypheny...)
Affinity DataIC50:  4.51E+3nMAssay Description:Tritiated E2 was incubated with 17beta-HSD2, cofactor, and inhibitor. The amount of labeled E1 formed was quantified by HPLC. Detection and quantific...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed