ID: ALA2288457

Max Phase: Preclinical

Molecular Formula: C10H12ClNOS

Molecular Weight: 229.73

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(OC(=S)N(C)C)ccc1Cl

Standard InChI:  InChI=1S/C10H12ClNOS/c1-7-6-8(4-5-9(7)11)13-10(14)12(2)3/h4-6H,1-3H3

Standard InChI Key:  WLRGHPLWXHMSLD-UHFFFAOYSA-N

Associated Targets(non-human)

Chilo suppressalis 440 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: 229.73Molecular Weight (Monoisotopic): 229.0328AlogP: 2.87#Rotatable Bonds: 1
Polar Surface Area: 12.47Molecular Species: HBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.70CX LogD: 3.70
Aromatic Rings: 1Heavy Atoms: 14QED Weighted: 0.69Np Likeness Score: -1.32

References

1. KONNO Y, SHISHIDO T.  (1990)  Aryl N, N-Dimethylcarbamates, Synergists for Organophosphorus Insecticides against Organophos-phorusresistant Rice Stem Borers,  15  (2): [10.1584/jpestics.15.175]

Source