<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">2947</id>
  <title>T3D2905</title>
  <common-name>Trifluoperazine</common-name>
  <description>Trifluoperazine is only found in individuals that have used or taken this drug. It is a phenothiazine with actions similar to chlorpromazine. It is used as an antipsychotic and an antiemetic. [PubChem]Trifluoperazine blocks postsynaptic mesolimbic dopaminergic D1 and D2 receptors in the brain; depresses the release of hypothalamic and hypophyseal hormones and is believed to depress the reticular activating system thus affecting basal metabolism, body temperature, wakefulness, vasomotor tone, and emesis.</description>
  <cas>117-89-5</cas>
  <pubchem-id>5566</pubchem-id>
  <chemical-formula>C21H24F3N3S</chemical-formula>
  <weight>407.164300</weight>
  <appearance>White powder.</appearance>
  <melting-point></melting-point>
  <boiling-point>202-210°C  at  6.00E-01 mm Hg</boiling-point>
  <density nil="true"/>
  <solubility>12.2 mg/L (at 24°C)</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Oral</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Trifluoperazine blocks postsynaptic mesolimbic dopaminergic D1 and D2 receptors in the brain; depresses the release of hypothalamic and hypophyseal hormones and is believed to depress the reticular activating system thus affecting basal metabolism, body temperature, wakefulness, vasomotor tone, and emesis.</mechanism-of-toxicity>
  <metabolism>Hepatic.Half Life: 10-20 hours</metabolism>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>For the treatment of anxiety disorders, depressive symptoms secondary to anxiety and agitation.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms>Symptoms of overdose include agitation, coma, convulsions, difficulty breathing, difficulty swallowing, dry mouth, extreme sleepiness, fever, intestinal blockage, irregular heart rate, low blood pressure, and restlessness.</symptoms>
  <treatment>Treatment is essentially symptomatic and supportive. Early gastric lavage is helpful. Keep patient under observation and maintain an open airway, since involvement of the extrapyramidal mechanism may produce dysphagia and respiratory difficulty in severe overdosage. Do not attempt to induce emesis because a dystonic reaction of the head or neck may develop that could result in aspiration of vomitus. Extrapyramidal symptoms may be treated with anti-parkinsonism drugs, barbiturates or Benadryl. See prescribing information for these products. Care should be taken to avoid increasing respiratory depression. If administration of a stimulant is desirable, amphetamine, dextroamphetamine or caffeine with sodium benzoate is recommended. Stimulants that may cause convulsions (e.g., picrotoxin or pentylenetetrazol) should be avoided. If hypotension occurs, the standard measures for managing circulatory shock should be initiated. If it is desirable to administer a vasoconstrictor, Levophed and Neo-Synephrine are most suitable. Other pressor agents, including epinephrine, are not recommended because phenothiazine derivatives may reverse the usual elevating action of these agents and cause a further lowering of blood pressure. (L1712)</treatment>
  <created-at type="dateTime">2009-07-21T20:27:45Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:25:53Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Trifluoperazine</wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>C07168</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>45951</chebi-id>
  <biocyc-id>CPD-7051</biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id>Trifluoperazine</stitch-id>
  <drugbank-id>DB00831</drugbank-id>
  <pdb-id>TFP</pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CN1CCN(CCCN2C3=CC=CC=C3SC3=C2C=C(C=C3)C(F)(F)F)CC1</moldb-smiles>
  <moldb-formula>C21H24F3N3S</moldb-formula>
  <moldb-inchi>InChI=1S/C21H24F3N3S/c1-25-11-13-26(14-12-25)9-4-10-27-17-5-2-3-6-19(17)28-20-8-7-16(15-18(20)27)21(22,23)24/h2-3,5-8,15H,4,9-14H2,1H3</moldb-inchi>
  <moldb-inchikey>InChIKey=ZEWQUBUPAILYHI-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">407.496</moldb-average-mass>
  <moldb-mono-mass type="decimal">407.164303088</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp>5.03</logp>
  <hmdb-id>HMDB14969</hmdb-id>
  <chembl-id>CHEMBL422</chembl-id>
  <chemspider-id>5365</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>
