2-Benzylsulfanyl-N-(2-oxo-tetrahydro-furan-3-yl)-acetamide

ID: ALA16014

Chembl Id: CHEMBL16014

PubChem CID: 21579076

Max Phase: Preclinical

Molecular Formula: C13H15NO3S

Molecular Weight: 265.33

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(CSCc1ccccc1)NC1CCOC1=O

Standard InChI:  InChI=1S/C13H15NO3S/c15-12(14-11-6-7-17-13(11)16)9-18-8-10-4-2-1-3-5-10/h1-5,11H,6-9H2,(H,14,15)

Standard InChI Key:  MXMHOTLWHVZXDY-UHFFFAOYSA-N

Alternative Forms

Associated Targets(non-human)

luxR Transcriptional activator protein luxR (400 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

Calculated Properties

Molecular Weight: 265.33Molecular Weight (Monoisotopic): 265.0773AlogP: 1.35#Rotatable Bonds: 5
Polar Surface Area: 55.40Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 12.25CX Basic pKa: CX LogP: 1.15CX LogD: 1.15
Aromatic Rings: 1Heavy Atoms: 18QED Weighted: 0.82Np Likeness Score: -1.09

References

1. Reverchon S, Chantegrel B, Deshayes C, Doutheau A, Cotte-Pattat N..  (2002)  New synthetic analogues of N-acyl homoserine lactones as agonists or antagonists of transcriptional regulators involved in bacterial quorum sensing.,  12  (8): [PMID:11934577] [10.1016/s0960-894x(02)00124-5]
2. 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