ID: ALA4103535

Max Phase: Preclinical

Molecular Formula: C10H13NO3

Molecular Weight: 195.22

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCOc1ccc(C(=O)OC)nc1

Standard InChI:  InChI=1S/C10H13NO3/c1-3-6-14-8-4-5-9(11-7-8)10(12)13-2/h4-5,7H,3,6H2,1-2H3

Standard InChI Key:  HRDJSKDJVGGLOM-UHFFFAOYSA-N

Associated Targets(non-human)

Regulatory protein RhlR 305 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: 195.22Molecular Weight (Monoisotopic): 195.0895AlogP: 1.66#Rotatable Bonds: 4
Polar Surface Area: 48.42Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.64CX LogP: 1.67CX LogD: 1.67
Aromatic Rings: 1Heavy Atoms: 14QED Weighted: 0.69Np Likeness Score: -1.01

References

1. Tung TT, Jakobsen TH, Dao TT, Fuglsang AT, Givskov M, Christensen SB, Nielsen J..  (2017)  Fusaric acid and analogues as Gram-negative bacterial quorum sensing inhibitors.,  126  [PMID:28033578] [10.1016/j.ejmech.2016.11.044]

Source