BENZYL PHENYLTHIOMETHYLCARBAMATE

ID: ALA2271155

Max Phase: Preclinical

Molecular Formula: C15H15NO2S

Molecular Weight: 273.36

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(NCSc1ccccc1)OCc1ccccc1

Standard InChI:  InChI=1S/C15H15NO2S/c17-15(18-11-13-7-3-1-4-8-13)16-12-19-14-9-5-2-6-10-14/h1-10H,11-12H2,(H,16,17)

Standard InChI Key:  CVZDMKUDXCBMCX-UHFFFAOYSA-N

Associated Targets(non-human)

Avena sativa 212 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

Properties

Molecular Weight: 273.36Molecular Weight (Monoisotopic): 273.0823AlogP: 3.66#Rotatable Bonds: 5
Polar Surface Area: 38.33Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.87CX Basic pKa: CX LogP: 3.61CX LogD: 3.61
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.67Np Likeness Score: -0.76

References

1. Alizadeh BH, Sugiyama T, Oritani T, Kuwahara S..  (2002)  Preparation of N-substituted aryl and alkyl carbamates and their inhibitory effect on oat seed germination.,  66  (2): [PMID:11999420] [10.1271/bbb.66.422]

Source