ID: ALA2287677

Max Phase: Preclinical

Molecular Formula: C21H11Cl3F5N3O3

Molecular Weight: 554.69

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C(=O)NC(=O)c1c(F)cccc1F)c1cc(Cl)c(Oc2ncc(C(F)(F)F)cc2Cl)c(Cl)c1

Standard InChI:  InChI=1S/C21H11Cl3F5N3O3/c1-32(20(34)31-18(33)16-14(25)3-2-4-15(16)26)10-6-11(22)17(12(23)7-10)35-19-13(24)5-9(8-30-19)21(27,28)29/h2-8H,1H3,(H,31,33,34)

Standard InChI Key:  YFULWRUONUHFEU-UHFFFAOYSA-N

Associated Targets(non-human)

Daphnia magna 43 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plutella xylostella 1838 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: 554.69Molecular Weight (Monoisotopic): 552.9786AlogP: 7.12#Rotatable Bonds: 4
Polar Surface Area: 71.53Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 8.92CX Basic pKa: 0.12CX LogP: 6.44CX LogD: 6.42
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.35Np Likeness Score: -1.58

References

1. KOYANAGI T, MORITA M, FUJII Y.  (1998)  Synthesis and Insecticidal Activity of Alkylated N-Benzoyl-N-Phenylureas and Their Toxicity to Aquatic Invertebrate,  23  (3): [10.1584/jpestics.23.250]

Source