ID: ALA2287670

Max Phase: Preclinical

Molecular Formula: C22H13ClF6N2O3

Molecular Weight: 502.80

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C(=O)NC(=O)c1c(F)cccc1F)c1ccc(Oc2ccc(C(F)(F)F)cc2Cl)c(F)c1

Standard InChI:  InChI=1S/C22H13ClF6N2O3/c1-31(21(33)30-20(32)19-14(24)3-2-4-15(19)25)12-6-8-18(16(26)10-12)34-17-7-5-11(9-13(17)23)22(27,28)29/h2-10H,1H3,(H,30,32,33)

Standard InChI Key:  UEQLIMFVTUJELN-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: 502.80Molecular Weight (Monoisotopic): 502.0519AlogP: 6.55#Rotatable Bonds: 4
Polar Surface Area: 58.64Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 8.92CX Basic pKa: CX LogP: 5.99CX LogD: 5.98
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.41Np Likeness Score: -1.62

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