ID: ALA3287839

Max Phase: Preclinical

Molecular Formula: C31H22O2

Molecular Weight: 426.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)c1ccc(/C=C/c2ccc3c(-c4ccccc4)ccc(-c4ccccc4)c3c2)cc1

Standard InChI:  InChI=1S/C31H22O2/c32-31(33)26-16-13-22(14-17-26)11-12-23-15-18-29-27(24-7-3-1-4-8-24)19-20-28(30(29)21-23)25-9-5-2-6-10-25/h1-21H,(H,32,33)/b12-11+

Standard InChI Key:  YQGZYHZTJDOJQB-VAWYXSNFSA-N

Associated Targets(Human)

Retinoid X receptor beta 726 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Retinoic acid receptor alpha 153 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Retinoic acid receptor beta 93 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Retinoic acid receptor gamma 95 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 426.52Molecular Weight (Monoisotopic): 426.1620AlogP: 8.04#Rotatable Bonds: 5
Polar Surface Area: 37.30Molecular Species: ACIDHBA: 1HBD: 1
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.12CX Basic pKa: CX LogP: 8.25CX LogD: 5.17
Aromatic Rings: 5Heavy Atoms: 33QED Weighted: 0.29Np Likeness Score: 0.11

References

1. Martínez C, Lieb M, Alvarez S, Rodríguez-Barrios F, Alvarez R, Khanwalkar H, Gronemeyer H, de Lera AR..  (2014)  Dual RXR Agonists and RAR Antagonists Based on the Stilbene Retinoid Scaffold.,  (5): [PMID:24900875] [10.1021/ml400521f]

Source