ID: ALA2253379

Max Phase: Preclinical

Molecular Formula: C15H13F5O2

Molecular Weight: 320.26

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)[C@H]1[C@H](C=Cc2c(F)c(F)c(F)c(F)c2F)C1(C)C

Standard InChI:  InChI=1S/C15H13F5O2/c1-15(2)7(8(15)14(21)22-3)5-4-6-9(16)11(18)13(20)12(19)10(6)17/h4-5,7-8H,1-3H3/t7-,8+/m0/s1

Standard InChI Key:  NMYAPULNYVVYSC-JGVFFNPUSA-N

Associated Targets(non-human)

Periplaneta americana 513 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ascia monuste 100 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Sitophilus zeamais 188 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acanthoscelides obtectus 18 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: 320.26Molecular Weight (Monoisotopic): 320.0836AlogP: 3.84#Rotatable Bonds: 3
Polar Surface Area: 26.30Molecular Species: HBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.03CX LogD: 4.03
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.37Np Likeness Score: 0.50

References

1. de Alvarenga ES, Carneiro VM, Resende GC, Picanço MC, Farias Ede S, Lopes MC..  (2012)  Synthesis and insecticidal activity of an oxabicyclolactone and novel pyrethroids.,  17  (12): [PMID:23183889] [10.3390/molecules171213989]

Source