ID: ALA305579

Max Phase: Preclinical

Molecular Formula: C17H12ClNO2

Molecular Weight: 297.74

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1ccc(Cl)cc1)c1ccc2ccccc2c1O

Standard InChI:  InChI=1S/C17H12ClNO2/c18-12-6-8-13(9-7-12)19-17(21)15-10-5-11-3-1-2-4-14(11)16(15)20/h1-10,20H,(H,19,21)

Standard InChI Key:  DMQGAZLVAUUHLW-UHFFFAOYSA-N

Associated Targets(Human)

THP-1 11052 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

Mycolicibacterium smegmatis 8003 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycobacterium kansasii 6484 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycobacterium marinum 465 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: 297.74Molecular Weight (Monoisotopic): 297.0557AlogP: 4.45#Rotatable Bonds: 2
Polar Surface Area: 49.33Molecular Species: NEUTRALHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.54CX Basic pKa: CX LogP: 4.36CX LogD: 4.12
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.73Np Likeness Score: -1.07

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]
2. Gonec T, Kos J, Zadrazilova I, Pesko M, Keltosova S, Tengler J, Bobal P, Kollar P, Cizek A, Kralova K, Jampilek J..  (2013)  Antimycobacterial and herbicidal activity of ring-substituted 1-hydroxynaphthalene-2-carboxanilides.,  21  (21): [PMID:24075143] [10.1016/j.bmc.2013.08.030]

Source