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N-2'-Thiazolin dodecanamide ID: ALA3753697
Chembl Id: CHEMBL3753697
PubChem CID: 3337578
Max Phase: Preclinical
Molecular Formula: C15H28N2OS
Molecular Weight: 284.47
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCCCCCCCCCCC(=O)NC1=NCCS1
Standard InChI: InChI=1S/C15H28N2OS/c1-2-3-4-5-6-7-8-9-10-11-14(18)17-15-16-12-13-19-15/h2-13H2,1H3,(H,16,17,18)
Standard InChI Key: ZUPVVNAGQBOEBB-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: 284.47Molecular Weight (Monoisotopic): 284.1922AlogP: 4.13#Rotatable Bonds: 10Polar Surface Area: 41.46Molecular Species: NEUTRALHBA: 3HBD: 1#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: 11.00CX Basic pKa: 5.94CX LogP: 4.84CX LogD: 4.82Aromatic Rings: 0Heavy Atoms: 19QED Weighted: 0.61Np Likeness Score: -0.68
References 1. Bucio-Cano A, Reyes-Arellano A, Correa-Basurto J, Bello M, Torres-Jaramillo J, Salgado-Zamora H, Curiel-Quesada E, Peralta-Cruz J, Avila-Sorrosa A.. (2015) Targeting quorum sensing by designing azoline derivatives to inhibit the N-hexanoyl homoserine lactone-receptor CviR: Synthesis as well as biological and theoretical evaluations., 23 (24): [PMID:26654469 ] [10.1016/j.bmc.2015.10.046 ]