ID: ALA2288444

Max Phase: Preclinical

Molecular Formula: C10H12ClNO2

Molecular Weight: 213.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCNC(=O)Oc1ccc(Cl)c(C)c1

Standard InChI:  InChI=1S/C10H12ClNO2/c1-3-12-10(13)14-8-4-5-9(11)7(2)6-8/h4-6H,3H2,1-2H3,(H,12,13)

Standard InChI Key:  IFENAKFRSKZMAR-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: 213.66Molecular Weight (Monoisotopic): 213.0557AlogP: 2.76#Rotatable Bonds: 2
Polar Surface Area: 38.33Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.94CX LogD: 2.94
Aromatic Rings: 1Heavy Atoms: 14QED Weighted: 0.82Np Likeness Score: -1.39

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