<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4603</id>
  <title>T3D4549</title>
  <common-name>Triticonazole</common-name>
  <description>Triticonazole is a seed treatment fungicide for the control of common bunt, loose smut and covered smut on barley, oats and wheat by inhibiting sterol demethylation.</description>
  <cas>131983-72-7</cas>
  <pubchem-id>86233</pubchem-id>
  <chemical-formula>C17H20ClN3O</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>Oral (rat) LD50: &gt;2000 mg/kg
Dermal (rat) LD50: &gt;2000 mg/kg
Inhalation (rat) LC50: &gt;1.4 mg/l/4h</toxicity>
  <lethaldose></lethaldose>
  <carcinogenicity>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>Triticonazole may cause irritation of eyes, skin, respiratory tract and lung injury. It can also cause burns of the esophagus or gastrointestinal tract. In animals (rat, mouse, rabbit and dog), some subchronic and chronic feeding studies show that triticonazole caused adrenal and liver toxicity. It caused some developmental, reproductive toxicity and maternal toxicity in rats and rabbits. Triticonazole was neither genotoxic nor carcinogenic and the U.S. Environmental Protection Agency (U.S. EPA) classified triticonazole as “not likely to be carcinogenic to humans.”</health-effects>
  <symptoms>Symptoms include headache, dizziness, weakness, and nausea.</symptoms>
  <treatment>For oral exposure, the gastric lavage can be used to remove some of the ingested triticonazole in conscious patients who still have airway protective reflexes and not intubated. Be aware of the potential complications of bleeding or perforation of esophageal or gastrointestinal tract. Activated charcoal can also be used to bind triticonazole and decrease its absorption. Drinking water or water may be of benefit too as soon as ingestion for immediate dilution. (L2112)</treatment>
  <created-at type="dateTime">2014-08-29T06:51:46Z</created-at>
  <updated-at type="dateTime">2026-03-31T18:33:50Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia></wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id></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>CC1(C)CCC(=CC2=CC=C(Cl)C=C2)C1(O)CN1C=NC=N1</moldb-smiles>
  <moldb-formula>C17H20ClN3O</moldb-formula>
  <moldb-inchi>InChI=1S/C17H20ClN3O/c1-16(2)8-7-14(9-13-3-5-15(18)6-4-13)17(16,22)10-21-12-19-11-20-21/h3-6,9,11-12,22H,7-8,10H2,1-2H3</moldb-inchi>
  <moldb-inchikey>PPDBOQMNKNNODG-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">317.813</moldb-average-mass>
  <moldb-mono-mass type="decimal">317.129489984</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp></logp>
  <hmdb-id></hmdb-id>
  <chembl-id>CHEMBL2356309</chembl-id>
  <chemspider-id>26461628</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"/>
  <chemdb-id>CHEM003509</chemdb-id>
  <dsstox-id>DTXSID0032655</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00010104</susdat-id>
  <iupac>5-[(4-chlorophenyl)methylidene]-2,2-dimethyl-1-[(1H-1,2,4-triazol-1-yl)methyl]cyclopentan-1-ol</iupac>
</compound>
