ID: ALA4293720

Max Phase: Preclinical

Molecular Formula: C18H23BrO3

Molecular Weight: 367.28

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C18H23BrO3/c1-14-12-18(20)22-17-13-15(8-9-16(14)17)21-11-7-5-3-2-4-6-10-19/h8-9,12-13H,2-7,10-11H2,1H3

Standard InChI Key:  GFRARDVTUANCDM-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: 367.28Molecular Weight (Monoisotopic): 366.0831AlogP: 5.22#Rotatable Bonds: 9
Polar Surface Area: 39.44Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.13CX LogD: 5.13
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.35Np Likeness Score: -0.22

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