ID: ALA2286557

Max Phase: Preclinical

Molecular Formula: C11H16N2O2

Molecular Weight: 208.26

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCO/N=C/Nc1ccc(OCC)cc1

Standard InChI:  InChI=1S/C11H16N2O2/c1-3-14-11-7-5-10(6-8-11)12-9-13-15-4-2/h5-9H,3-4H2,1-2H3,(H,12,13)

Standard InChI Key:  VBPVVVRFNAIKAN-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: 208.26Molecular Weight (Monoisotopic): 208.1212AlogP: 2.48#Rotatable Bonds: 6
Polar Surface Area: 42.85Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.97CX LogP: 2.11CX LogD: 2.11
Aromatic Rings: 1Heavy Atoms: 15QED Weighted: 0.44Np Likeness Score: -1.15

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