ID: ALA58209

Max Phase: Preclinical

Molecular Formula: C17H19FO3

Molecular Weight: 290.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(/C=C/C=C(\C)COc1ccc(F)cc1C)=C\C(=O)O

Standard InChI:  InChI=1S/C17H19FO3/c1-12(9-17(19)20)5-4-6-13(2)11-21-16-8-7-15(18)10-14(16)3/h4-10H,11H2,1-3H3,(H,19,20)/b5-4+,12-9+,13-6+

Standard InChI Key:  PMJNZLWSQZJNHJ-QPCGNHOSSA-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: 290.33Molecular Weight (Monoisotopic): 290.1318AlogP: 4.05#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: 4.17CX LogD: 1.31
Aromatic Rings: 1Heavy Atoms: 21QED Weighted: 0.63Np Likeness Score: 0.39

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