ID: ALA2272488

Max Phase: Preclinical

Molecular Formula: C21H17NO2

Molecular Weight: 315.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1ccc([C@H]2O[C@@H]2C(=O)c2ccc(-c3ccccc3)cc2)cc1

Standard InChI:  InChI=1S/C21H17NO2/c22-18-12-10-17(11-13-18)20-21(24-20)19(23)16-8-6-15(7-9-16)14-4-2-1-3-5-14/h1-13,20-21H,22H2/t20-,21-/m1/s1

Standard InChI Key:  UXXLTEALIGHBAP-NHCUHLMSSA-N

Associated Targets(non-human)

Enterococcus faecalis 29875 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Proteus vulgaris 5823 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Klebsiella 302 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas 460 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 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: 315.37Molecular Weight (Monoisotopic): 315.1259AlogP: 4.26#Rotatable Bonds: 4
Polar Surface Area: 55.62Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.08CX LogP: 4.00CX LogD: 4.00
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.44Np Likeness Score: 0.07

References

1. Thirunarayanan G, Vanangamudi G.  (2011)  Synthesis, spectral studies, antimicrobial and insect antifeedant potent keto oxiranes,  [10.1016/j.arabjc.2011.03.020]

Source