ID: ALA65408

Max Phase: Preclinical

Molecular Formula: C19H16ClNO2

Molecular Weight: 325.80

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(NCCc1ccc(Cl)cc1)c1cc2ccccc2cc1O

Standard InChI:  InChI=1S/C19H16ClNO2/c20-16-7-5-13(6-8-16)9-10-21-19(23)17-11-14-3-1-2-4-15(14)12-18(17)22/h1-8,11-12,22H,9-10H2,(H,21,23)

Standard InChI Key:  AWDPSKHWWLVOBV-UHFFFAOYSA-N

Associated Targets(Human)

DNA polymerase alpha subunit 225 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HFF 3142 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

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: 325.80Molecular Weight (Monoisotopic): 325.0870AlogP: 4.17#Rotatable Bonds: 4
Polar Surface Area: 49.33Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.97CX Basic pKa: CX LogP: 5.00CX LogD: 4.90
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.76Np Likeness Score: -0.76

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