ID: ALA4579576

Max Phase: Preclinical

Molecular Formula: C14H21NO4

Molecular Weight: 267.32

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(CC(=O)N[C@H]1CCOC1=O)CC1CCCCC1

Standard InChI:  InChI=1S/C14H21NO4/c16-11(8-10-4-2-1-3-5-10)9-13(17)15-12-6-7-19-14(12)18/h10,12H,1-9H2,(H,15,17)/t12-/m0/s1

Standard InChI Key:  WFKGCUDGFYJDBT-LBPRGKRZSA-N

Associated Targets(non-human)

Transcriptional activator protein luxR 400 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 267.32Molecular Weight (Monoisotopic): 267.1471AlogP: 1.35#Rotatable Bonds: 5
Polar Surface Area: 72.47Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.11CX Basic pKa: CX LogP: 1.44CX LogD: 1.44
Aromatic Rings: 0Heavy Atoms: 19QED Weighted: 0.60Np Likeness Score: -0.04

References

1. Chbib C..  (2020)  Impact of the structure-activity relationship of AHL analogues on quorum sensing in Gram-negative bacteria.,  28  (3): [PMID:31918952] [10.1016/j.bmc.2019.115282]

Source