ID: ALA398654

Max Phase: Preclinical

Molecular Formula: C14H8F3NO2

Molecular Weight: 279.22

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Oc1ccc(-c2nc3ccccc3o2)cc1C(F)(F)F

Standard InChI:  InChI=1S/C14H8F3NO2/c15-14(16,17)9-7-8(5-6-11(9)19)13-18-10-3-1-2-4-12(10)20-13/h1-7,19H

Standard InChI Key:  KZMZENFTOPNAQP-UHFFFAOYSA-N

Associated Targets(Human)

TTR Tclin Transthyretin (2847 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRA Tclin Thyroid hormone receptor (146 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: 279.22Molecular Weight (Monoisotopic): 279.0507AlogP: 4.22#Rotatable Bonds: 1
Polar Surface Area: 46.26Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.43CX Basic pKa: 0.18CX LogP: 3.92CX LogD: 3.63
Aromatic Rings: 3Heavy Atoms: 20QED Weighted: 0.73Np Likeness Score: -0.90

References

1. Johnson SM, Connelly S, Wilson IA, Kelly JW..  (2008)  Biochemical and structural evaluation of highly selective 2-arylbenzoxazole-based transthyretin amyloidogenesis inhibitors.,  51  (2): [PMID:18095641] [10.1021/jm0708735]

Source