ID: ALA2286280

Max Phase: Preclinical

Molecular Formula: C13H20N2O3

Molecular Weight: 252.31

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCO/N=C/Nc1ccc(OCC)c(OCC)c1

Standard InChI:  InChI=1S/C13H20N2O3/c1-4-16-12-8-7-11(9-13(12)17-5-2)14-10-15-18-6-3/h7-10H,4-6H2,1-3H3,(H,14,15)

Standard InChI Key:  ZXGIXMQMEPPOSL-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: 252.31Molecular Weight (Monoisotopic): 252.1474AlogP: 2.88#Rotatable Bonds: 8
Polar Surface Area: 52.08Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.71CX LogP: 2.30CX LogD: 2.30
Aromatic Rings: 1Heavy Atoms: 18QED Weighted: 0.44Np Likeness Score: -1.00

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