ID: ALA3805876

Max Phase: Preclinical

Molecular Formula: C11H7FN2O3

Molecular Weight: 234.19

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1Cn2c(cc3cc(F)ccc32)C(=O)N1O

Standard InChI:  InChI=1S/C11H7FN2O3/c12-7-1-2-8-6(3-7)4-9-11(16)14(17)10(15)5-13(8)9/h1-4,17H,5H2

Standard InChI Key:  JSKMANVPEGGBAC-UHFFFAOYSA-N

Associated Targets(non-human)

Polymerase acidic protein 35 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hepatitis C virus 23859 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: 234.19Molecular Weight (Monoisotopic): 234.0441AlogP: 1.15#Rotatable Bonds: 0
Polar Surface Area: 62.54Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.17CX Basic pKa: CX LogP: 0.90CX LogD: 0.47
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.55Np Likeness Score: -1.07

References

1. Zoidis G, Giannakopoulou E, Stevaert A, Frakolaki E, Myrianthopoulos V, Fytas G, Mavromara P, Mikros E, Bartenschlager R, Vassilaki N, Naesens L.  (2016)  Novel indoleflutimide heterocycles with activity against influenza PA endonuclease and hepatitis C virus,  (3): [10.1039/C5MD00439J]

Source