ID: ALA515217

Max Phase: Preclinical

Molecular Formula: C14H11F6NO3

Molecular Weight: 355.23

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)N[C@H]1CCOC1=O

Standard InChI:  InChI=1S/C14H11F6NO3/c15-13(16,17)8-3-7(4-9(6-8)14(18,19)20)5-11(22)21-10-1-2-24-12(10)23/h3-4,6,10H,1-2,5H2,(H,21,22)/t10-/m0/s1

Standard InChI Key:  MPBHYAGAWNMEHP-JTQLQIEISA-N

Associated Targets(non-human)

Transcriptional activator protein traR 147 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Transcriptional activator protein luxR 62 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: 355.23Molecular Weight (Monoisotopic): 355.0643AlogP: 2.70#Rotatable Bonds: 3
Polar Surface Area: 55.40Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.00CX Basic pKa: CX LogP: 2.51CX LogD: 2.51
Aromatic Rings: 1Heavy Atoms: 24QED Weighted: 0.67Np Likeness Score: -0.75

References

1. Geske GD, Mattmann ME, Blackwell HE..  (2008)  Evaluation of a focused library of N-aryl L-homoserine lactones reveals a new set of potent quorum sensing modulators.,  18  (22): [PMID:18760602] [10.1016/j.bmcl.2008.07.089]

Source