<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">3860</id>
  <title>T3D3805</title>
  <common-name>Carfentrazone-ethyl</common-name>
  <description>Carfentrazone-ethyl is a contact herbicide used to control broadleaf and sedge weeds in cereals.  The mode of action of carfentrazone-ethyl is the disruption of membranes by inhibiting the action of protoporphyrinogen oxidase, causing cell death.  Carfentrazone is non-selective, and can be used for complete vegetation control, as well as as a desiccant and a defoliant in some crops.  </description>
  <cas>128639-02-1</cas>
  <pubchem-id>86222</pubchem-id>
  <chemical-formula>C15H14Cl2F3N3O3</chemical-formula>
  <weight nil="true"/>
  <appearance>White powder.</appearance>
  <melting-point></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>LD50 (rat, oral) &gt;5000 mg/kg
LD50 (rat, dermal) &gt;4000 mg/kg
LC50 (rat, inhalation) &gt;5.09 mg/L</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>Carfentrazone-ethyl is not considered to cause significant toxicity in helathy humans. But in patient with very large acute exposures or long-term chronic exposures, carfentrazone-ethyl may cause variegate porphyria or transient porphyria cutanea tarda-like syndrome. (L2125)</health-effects>
  <symptoms></symptoms>
  <treatment>Remove contaminated clothing and wash skin with soap and water. For eye exposure, copious irrigation with water or saline is used. The treatment is usually symptomatic and supportive.</treatment>
  <created-at type="dateTime">2013-04-25T07:56:50Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:26:32Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia></wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>C11094</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id></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>CCOC(=O)C(Cl)CC1=C(Cl)C=C(F)C(=C1)N1N=C(C)N(C(F)F)C1=O</moldb-smiles>
  <moldb-formula>C15H14Cl2F3N3O3</moldb-formula>
  <moldb-inchi>InChI=1S/C15H14Cl2F3N3O3/c1-3-26-13(24)10(17)4-8-5-12(11(18)6-9(8)16)23-15(25)22(14(19)20)7(2)21-23/h5-6,10,14H,3-4H2,1-2H3</moldb-inchi>
  <moldb-inchikey>InChIKey=MLKCGVHIFJBRCD-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">412.191</moldb-average-mass>
  <moldb-mono-mass type="decimal">411.036431358</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp></logp>
  <hmdb-id></hmdb-id>
  <chembl-id>CHEMBL2145069</chembl-id>
  <chemspider-id>77773</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>
