ID: ALA4517457

Max Phase: Preclinical

Molecular Formula: C13H19NO4

Molecular Weight: 253.30

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(CC(=O)N[C@H]1CCOC1=O)CC1CCCC1

Standard InChI:  InChI=1S/C13H19NO4/c15-10(7-9-3-1-2-4-9)8-12(16)14-11-5-6-18-13(11)17/h9,11H,1-8H2,(H,14,16)/t11-/m0/s1

Standard InChI Key:  WEFSXAMEWPDYBJ-NSHDSACASA-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: 253.30Molecular Weight (Monoisotopic): 253.1314AlogP: 0.96#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: 10.10CX Basic pKa: CX LogP: 1.00CX LogD: 1.00
Aromatic Rings: 0Heavy Atoms: 18QED Weighted: 0.58Np Likeness Score: -0.02

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