<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">2797</id>
  <title>T3D2755</title>
  <common-name>Metixene</common-name>
  <description>Metixene is only found in individuals that have used or taken this drug. It is a anticholinergic used as an anti-parkinson drug. </description>
  <cas>4969-02-2</cas>
  <pubchem-id>4167</pubchem-id>
  <chemical-formula>C20H23NS</chemical-formula>
  <weight>309.155120</weight>
  <appearance nil="true"/>
  <melting-point>&lt; 25°C</melting-point>
  <boiling-point>173°C at 7.00E-02 mm Hg</boiling-point>
  <density nil="true"/>
  <solubility>Soluble as HCl salt</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Absorbed in the gastrointestinal tract following oral administration, however the extent of absorption is not known.</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Parkinsonism is thought to result from an imbalance between the excitatory (cholinergic) and inhibitory (dopaminergic) systems in the corpus striatum. The mechanism of action of centrally active anticholinergic drugs such as metixene is considered to relate to competitive antagonism of acetylcholine at muscarinic receptors in the corpus striatum, which then restores the balance.</mechanism-of-toxicity>
  <metabolism>Hepatic. Metabolism occurs via sulfoxydation and N-demethylation.</metabolism>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>Used for the symptomatic treatment of parkinsonism.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms>Signs of overdose include dilated and sluggish pupils, warm, dry skin, facial flushing, decreased secretions of the mouth, pharynx, nose, and bronchi, foul-smelling breath, elevated temperature, tachycardia, cardiac arrhythmias, decreased bowel sounds, urinary retention, delirium, disorientation, anxiety, hallucinations, illusions, confusion, incoherence, agitation, hyperactivity, ataxia, loss of memory, paranoia, combativeness, and seizures.</symptoms>
  <treatment nil="true"/>
  <created-at type="dateTime">2009-07-21T20:26:38Z</created-at>
  <updated-at type="dateTime">2026-03-31T17:57:08Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Metixene</wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id></kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>51024</chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id>Metixene</stitch-id>
  <drugbank-id>DB00340</drugbank-id>
  <pdb-id></pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CN1CCCC(CC2C3=CC=CC=C3SC3=CC=CC=C23)C1</moldb-smiles>
  <moldb-formula>C20H23NS</moldb-formula>
  <moldb-inchi>InChI=1S/C20H23NS/c1-21-12-6-7-15(14-21)13-18-16-8-2-4-10-19(16)22-20-11-5-3-9-17(18)20/h2-5,8-11,15,18H,6-7,12-14H2,1H3</moldb-inchi>
  <moldb-inchikey>MJFJKKXQDNNUJF-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">309.468</moldb-average-mass>
  <moldb-mono-mass type="decimal">309.155120431</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Liquid</state>
  <logp>4.7</logp>
  <hmdb-id>HMDB14484</hmdb-id>
  <chembl-id nil="true"/>
  <chemspider-id>4023</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>CHEM002174</chemdb-id>
  <dsstox-id>DTXSID1047867</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00009750</susdat-id>
  <iupac>1-methyl-3-(9H-thioxanthen-9-ylmethyl)piperidine</iupac>
</compound>
