3-(methoxymethoxy)-N-(4-nitrophenyl)naphthalene-2-carboxamide

ID: ALA63723

Max Phase: Preclinical

Molecular Formula: C19H16N2O5

Molecular Weight: 352.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COCOc1cc2ccccc2cc1C(=O)Nc1ccc([N+](=O)[O-])cc1

Standard InChI:  InChI=1S/C19H16N2O5/c1-25-12-26-18-11-14-5-3-2-4-13(14)10-17(18)19(22)20-15-6-8-16(9-7-15)21(23)24/h2-11H,12H2,1H3,(H,20,22)

Standard InChI Key:  OSRAPSLHEARREC-UHFFFAOYSA-N

Associated Targets(non-human)

U38 Human herpesvirus 6 DNA polymerase (36 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: 352.35Molecular Weight (Monoisotopic): 352.1059AlogP: 3.98#Rotatable Bonds: 6
Polar Surface Area: 90.70Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.90CX LogD: 3.90
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.41Np Likeness Score: -1.15

References

1. Vaillancourt VA, Cudahy MM, Staley SA, Brideau RJ, Conrad SJ, Knechtel ML, Oien NL, Wieber JL, Yagi Y, Wathen MW..  (2000)  Naphthalene carboxamides as inhibitors of human cytomegalovirus DNA polymerase.,  10  (18): [PMID:10999475] [10.1016/s0960-894x(00)00402-9]

Source