ID: ALA56986

Max Phase: Preclinical

Molecular Formula: C19H24O3

Molecular Weight: 300.40

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(/C=C/C=C(\C)COc1cc(C)cc(C)c1C)=C\C(=O)O

Standard InChI:  InChI=1S/C19H24O3/c1-13(11-19(20)21)7-6-8-14(2)12-22-18-10-15(3)9-16(4)17(18)5/h6-11H,12H2,1-5H3,(H,20,21)/b7-6+,13-11+,14-8+

Standard InChI Key:  CAAYHNFWDVSNMH-ZBFYLJCLSA-N

Associated Targets(Human)

Cellular retinoic acid-binding protein I 14 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus 284745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Retinoic acid receptor alpha 153 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: 300.40Molecular Weight (Monoisotopic): 300.1725AlogP: 4.52#Rotatable Bonds: 6
Polar Surface Area: 46.53Molecular Species: ACIDHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.44CX Basic pKa: CX LogP: 5.05CX LogD: 2.20
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.62Np Likeness Score: 0.74

References

1. Shealy YF, Riordan JM, Frye JL, Simpson-Herren L, Sani BP, Hill DL..  (2003)  Inhibition of papilloma formation by analogues of 7,8-dihydroretinoic acid.,  46  (10): [PMID:12723955] [10.1021/jm020324t]

Source