ID: ALA2287913

Max Phase: Preclinical

Molecular Formula: C12H17F3N2O3

Molecular Weight: 294.27

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCN(C)C(=O)COc1onc(C(F)(F)F)c1C

Standard InChI:  InChI=1S/C12H17F3N2O3/c1-4-5-6-17(3)9(18)7-19-11-8(2)10(16-20-11)12(13,14)15/h4-7H2,1-3H3

Standard InChI Key:  YSYKTWOAYUMPDT-UHFFFAOYSA-N

Associated Targets(non-human)

Persicaria lapathifolia 57 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: 294.27Molecular Weight (Monoisotopic): 294.1191AlogP: 2.64#Rotatable Bonds: 6
Polar Surface Area: 55.57Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.49CX LogD: 2.49
Aromatic Rings: 1Heavy Atoms: 20QED Weighted: 0.81Np Likeness Score: -1.55

References

1. KAI H, HORITA Y, MIKI N, IDE K, TAKASE A.  (1998)  Synthesis and Herbicidal Activities of 2-(5-Isoxazolyloxy)-acetamide Derivatives,  23  (3): [10.1584/jpestics.23.255]

Source