ID: ALA4283129

Max Phase: Preclinical

Molecular Formula: C21H26N2O3

Molecular Weight: 354.45

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(=O)oc2cc(OCCCCCCCCn3ccnc3)ccc12

Standard InChI:  InChI=1S/C21H26N2O3/c1-17-14-21(24)26-20-15-18(8-9-19(17)20)25-13-7-5-3-2-4-6-11-23-12-10-22-16-23/h8-10,12,14-16H,2-7,11,13H2,1H3

Standard InChI Key:  OPJHRADBNBNRLR-UHFFFAOYSA-N

Associated Targets(non-human)

Flavobacterium columnare 138 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptococcus agalactiae 1777 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: 354.45Molecular Weight (Monoisotopic): 354.1943AlogP: 4.72#Rotatable Bonds: 10
Polar Surface Area: 57.26Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.54CX LogP: 4.19CX LogD: 4.15
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.39Np Likeness Score: -0.83

References

1. Hu Y, Shen Y, Wu X, Tu X, Wang GX..  (2018)  Synthesis and biological evaluation of coumarin derivatives containing imidazole skeleton as potential antibacterial agents.,  143  [PMID:29232586] [10.1016/j.ejmech.2017.11.100]

Source