ID: ALA2297084

Max Phase: Preclinical

Molecular Formula: C20H14N2O4

Molecular Weight: 346.34

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1CC2c3ccc4ccccc4c3OC2N1c1ccc([N+](=O)[O-])cc1

Standard InChI:  InChI=1S/C20H14N2O4/c23-18-11-17-16-10-5-12-3-1-2-4-15(12)19(16)26-20(17)21(18)13-6-8-14(9-7-13)22(24)25/h1-10,17,20H,11H2

Standard InChI Key:  WKMBACBNMFMYOD-UHFFFAOYSA-N

Associated Targets(non-human)

Cladosporium 17 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alternaria 24 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium graminearum 1554 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Micrococcus luteus 7463 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 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: 346.34Molecular Weight (Monoisotopic): 346.0954AlogP: 3.99#Rotatable Bonds: 2
Polar Surface Area: 72.68Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.61CX LogD: 3.61
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.52Np Likeness Score: -0.20

References

1. Soman SS, Thaker TH.  (2013)  Synthesis of tetracyclic aza-/oxa-naphthalen-8-ones and their antimicrobial activity,  22  (9): [10.1007/s00044-012-0425-z]

Source