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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
Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 265.33Molecular Weight (Monoisotopic): 265.0773AlogP: 1.35#Rotatable Bonds: 5Polar 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: 1.15Aromatic 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 ]