ID: ALA3414862

Max Phase: Preclinical

Molecular Formula: C17H12F3NO3

Molecular Weight: 335.28

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1Cc2cc(Cc3ccc(C(F)(F)F)cc3)ccc2C(=O)N1O

Standard InChI:  InChI=1S/C17H12F3NO3/c18-17(19,20)13-4-1-10(2-5-13)7-11-3-6-14-12(8-11)9-15(22)21(24)16(14)23/h1-6,8,24H,7,9H2

Standard InChI Key:  UBHLPWPNFMBLAM-UHFFFAOYSA-N

Associated Targets(non-human)

pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
gag-pol Moloney murine leukaemia virus Pol protein (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pol Human immunodeficiency virus type 1 integrase (9041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus (3636 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: 335.28Molecular Weight (Monoisotopic): 335.0769AlogP: 3.21#Rotatable Bonds: 2
Polar Surface Area: 57.61Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.32CX Basic pKa: CX LogP: 3.64CX LogD: 3.30
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.68Np Likeness Score: -0.32

References

1. Vernekar SK, Liu Z, Nagy E, Miller L, Kirby KA, Wilson DJ, Kankanala J, Sarafianos SG, Parniak MA, Wang Z..  (2015)  Design, synthesis, biochemical, and antiviral evaluations of C6 benzyl and C6 biarylmethyl substituted 2-hydroxylisoquinoline-1,3-diones: dual inhibition against HIV reverse transcriptase-associated RNase H and polymerase with antiviral activities.,  58  (2): [PMID:25522204] [10.1021/jm501132s]

Source