ID: ALA2441135

Max Phase: Preclinical

Molecular Formula: C18H15NO3

Molecular Weight: 293.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cccc(NC(=O)c2ccc3ccccc3c2O)c1

Standard InChI:  InChI=1S/C18H15NO3/c1-22-14-7-4-6-13(11-14)19-18(21)16-10-9-12-5-2-3-8-15(12)17(16)20/h2-11,20H,1H3,(H,19,21)

Standard InChI Key:  UDERNFGBTUHGFH-UHFFFAOYSA-N

Associated Targets(non-human)

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: 293.32Molecular Weight (Monoisotopic): 293.1052AlogP: 3.81#Rotatable Bonds: 3
Polar Surface Area: 58.56Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.54CX Basic pKa: CX LogP: 3.59CX LogD: 3.36
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.77Np Likeness Score: -0.96

References

1. 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