Details of the Drug

General Information of Drug (ID: DM2T4NL)

Drug Name
1-Bromo-6-(4-hydroxy-phenyl)-naphthalen-2-ol
Synonyms CHEMBL194936; 1-Bromo-6-(4-hydroxy-phenyl)-naphthalen-2-ol; SCHEMBL3936480; IPBYYNRPJBGKET-UHFFFAOYSA-N; ZINC13645011; BDBM50168334
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Drug Type
Small molecular drug
Structure
3D MOL 2D MOL
#Ro5 Violations (Lipinski): 0 Molecular Weight (mw) 315.16
Logarithm of the Partition Coefficient (xlogp) 4.8
Rotatable Bond Count (rotbonds) 1
Hydrogen Bond Donor Count (hbonddonor) 2
Hydrogen Bond Acceptor Count (hbondacc) 2
Chemical Identifiers
Formula
C16H11BrO2
IUPAC Name
1-bromo-6-(4-hydroxyphenyl)naphthalen-2-ol
Canonical SMILES
C1=CC(=CC=C1C2=CC3=C(C=C2)C(=C(C=C3)O)Br)O
InChI
InChI=1S/C16H11BrO2/c17-16-14-7-3-11(9-12(14)4-8-15(16)19)10-1-5-13(18)6-2-10/h1-9,18-19H
InChIKey
IPBYYNRPJBGKET-UHFFFAOYSA-N
Cross-matching ID
PubChem CID
10149684
TTD ID
D0S6NV

Molecular Interaction Atlas of This Drug


Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Estrogen receptor (ESR) TTZAYWL ESR1_HUMAN Inhibitor [1]
Estrogen receptor beta (ESR2) TTOM3J0 ESR2_HUMAN Inhibitor [1]
Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This Drug

References

1 ERbeta ligands. 3. Exploiting two binding orientations of the 2-phenylnaphthalene scaffold to achieve ERbeta selectivity. J Med Chem. 2005 Jun 16;48(12):3953-79.