ID: ALA2286564

Max Phase: Preclinical

Molecular Formula: C11H16N2O

Molecular Weight: 192.26

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCO/N=C/Nc1cc(C)cc(C)c1

Standard InChI:  InChI=1S/C11H16N2O/c1-4-14-13-8-12-11-6-9(2)5-10(3)7-11/h5-8H,4H2,1-3H3,(H,12,13)

Standard InChI Key:  LBAHOEKRKTVXME-UHFFFAOYSA-N

Associated Targets(non-human)

Phaseolus vulgaris 518 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Botrytis cinerea 4183 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: 192.26Molecular Weight (Monoisotopic): 192.1263AlogP: 2.70#Rotatable Bonds: 4
Polar Surface Area: 33.62Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.78CX LogP: 2.93CX LogD: 2.93
Aromatic Rings: 1Heavy Atoms: 14QED Weighted: 0.45Np Likeness Score: -0.88

References

1. HAYAKAWA K, NAKAYAMA A, NISHIKAWA H, NAKATA A, SANO S, YOKOTA C.  (1992)  Quantitative Structure-Activity Relationships of Fungicidal N-Phenylformamidoximes,  17  (1): [10.1584/jpestics.17.17]

Source