<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">3889</id>
  <title>T3D3834</title>
  <common-name>Etoxazole</common-name>
  <description>Etoxazole is an insecticide use to control spider mites infesting indoor (greenhouse, lath and shade house) grown ornamental crops including flowering and foliage crops, ground covers, shrubs and trees and non-bearing fruit and nuts trees. Etoxazole is a member of the oxazoline class of insecticides. It kills mite eggs and nymphs and prevents adults from laying viable eggs. Etoxazole is readily absorbed by the plant and will translocate locally in the leaf. The insecticidal mode of action of etoxazole is chitin biosynthesis inhibition. Etoxazole induces moulting defects in fall armyworm larvae similar to those caused by benzoylphenylureas, a well-known class of insecticidal chitin biosynthesis inhibitors.</description>
  <cas>153233-91-1</cas>
  <pubchem-id>153974</pubchem-id>
  <chemical-formula>C21H23F2NO2</chemical-formula>
  <weight nil="true"/>
  <appearance>White, crystalline powder.</appearance>
  <melting-point>101-102 deg C</melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility></solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure></route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity></mechanism-of-toxicity>
  <metabolism></metabolism>
  <toxicity></toxicity>
  <lethaldose></lethaldose>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>This is a man-made compound that is used as a pesticide.</use-source>
  <min-risk-level></min-risk-level>
  <health-effects></health-effects>
  <symptoms></symptoms>
  <treatment></treatment>
  <created-at type="dateTime">2013-04-25T07:56:51Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:26:33Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia></wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>C18495</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>39329</chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id></ctd-id>
  <stitch-id></stitch-id>
  <drugbank-id></drugbank-id>
  <pdb-id></pdb-id>
  <actor-id></actor-id>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CCOC1=C(C=CC(=C1)C(C)(C)C)C1COC(=N1)C1=C(F)C=CC=C1F</moldb-smiles>
  <moldb-formula>C21H23F2NO2</moldb-formula>
  <moldb-inchi>InChI=1S/C21H23F2NO2/c1-5-25-18-11-13(21(2,3)4)9-10-14(18)17-12-26-20(24-17)19-15(22)7-6-8-16(19)23/h6-11,17H,5,12H2,1-4H3</moldb-inchi>
  <moldb-inchikey>InChIKey=IXSZQYVWNJNRAL-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">359.4096</moldb-average-mass>
  <moldb-mono-mass type="decimal">359.169685395</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp></logp>
  <hmdb-id></hmdb-id>
  <chembl-id>CHEMBL1881674</chembl-id>
  <chemspider-id>135707</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference></synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
