<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">2761</id>
  <title>T3D2719</title>
  <common-name>Temazepam</common-name>
  <description>Temazepam is only found in individuals that have used or taken this drug. It is a benzodiazepine that acts as a gamma-aminobutyric acid modulator and anti-anxiety agent. [PubChem]Benzodiazepines bind nonspecifically to benzodiazepine receptors, which affects muscle relaxation, anticonvulsant activity, motor coordination, and memory. As benzodiazepine receptors are thought to be coupled to gamma-aminobutyric acid-A (GABA&lt;sub&gt;A&lt;/sub&gt;) receptors, this enhances the effects of GABA by increasing GABA affinity for the GABA receptor. Binding of the inhibitory neurotransmitter GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.</description>
  <cas>846-50-4</cas>
  <pubchem-id>5391</pubchem-id>
  <chemical-formula>C16H13ClN2O2</chemical-formula>
  <weight>300.066550</weight>
  <appearance>White powder.</appearance>
  <melting-point>119-121°C</melting-point>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility>164 mg/L</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Oral, well absorbed, minimal first-pass metabolism.</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Benzodiazepines bind nonspecifically to benzodiazepine receptors, which affects muscle relaxation, anticonvulsant activity, motor coordination, and memory. As benzodiazepine receptors are thought to be coupled to gamma-aminobutyric acid-A (GABA&lt;sub&gt;A&lt;/sub&gt;) receptors, this enhances the effects of GABA by increasing GABA affinity for the GABA receptor. Binding of the inhibitory neurotransmitter GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.</mechanism-of-toxicity>
  <metabolism>Hepatic. Temazepam is completely metabolized through conjugation prior to excretion. The major metabolite is the O-conjugate of temazepam (90%).Route of Elimination: Temazepam was completely metabolized through conjugation prior to excretion; 80% to 90% of the dose appeared in the urine.Half Life: 10-20 hours</metabolism>
  <toxicity>LD50: 1963 mg/kg (oral, mice) (L1338)
LD50: 1833 mg/kg (oral, rat) (L1338)
LD50: &gt;2400 mg/kg (oral, rabbit) (L1338)</toxicity>
  <lethaldose nil="true"/>
  <carcinogenicity>3, not classifiable as to its carcinogenicity to humans. (L135)</carcinogenicity>
  <use-source>Officially indicated for severe insomnia and other severe or disabling sleep disorders. For the short-term treatment of insomnia (generally 7-10 days).</use-source>
  <min-risk-level nil="true"/>
  <health-effects>They cause slurred speech, disorientation and "drunken" behavior. They are physically and psychologically addictive.</health-effects>
  <symptoms nil="true"/>
  <treatment>If the patient is conscious, vomiting should be induced mechanically or with emetics. Gastric lavage should be employed utilizing concurrently a cuffed endotracheal tube if the patient is unconscious to prevent aspiration and pulmonary complications. Maintenance of adequate pulmonary ventilation is essential. The use of pressor agents intravenously may be necessary to combat hypotension. Fluids should be administered intravenously to encourage diuresis. (L1712)</treatment>
  <created-at type="dateTime">2009-07-21T20:26:20Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:25:50Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Temazepam</wikipedia>
  <uniprot-id></uniprot-id>
  <kegg-compound-id>C07125</kegg-compound-id>
  <omim-id></omim-id>
  <chebi-id>195909</chebi-id>
  <biocyc-id></biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id>Temazepam</stitch-id>
  <drugbank-id>DB00231</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>CN1C2=C(C=C(Cl)C=C2)C(=NC(O)C1=O)C1=CC=CC=C1</moldb-smiles>
  <moldb-formula>C16H13ClN2O2</moldb-formula>
  <moldb-inchi>InChI=1/C16H13ClN2O2/c1-19-13-8-7-11(17)9-12(13)14(18-15(20)16(19)21)10-5-3-2-4-6-10/h2-9,15,20H,1H3</moldb-inchi>
  <moldb-inchikey>InChIKey=SEQDDYPDSLOBDC-UHFFFAOYNA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">300.74</moldb-average-mass>
  <moldb-mono-mass type="decimal">300.066555377</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Solid</state>
  <logp>2.19</logp>
  <hmdb-id>HMDB14376</hmdb-id>
  <chembl-id>CHEMBL967</chembl-id>
  <chemspider-id>5198</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>
