<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4608</id>
  <title>T3D4554</title>
  <common-name>Brompheniramine</common-name>
  <description>Histamine H1 antagonist used in treatment of allergies, rhinitis, and urticaria. [PubChem]</description>
  <cas>86-22-6</cas>
  <pubchem-id>6834</pubchem-id>
  <chemical-formula>C16H19BrN2</chemical-formula>
  <weight nil="true"/>
  <appearance nil="true"/>
  <melting-point>&lt; 25 °C</melting-point>
  <boiling-point>149.5 °C at 5.00E-01 mm Hg</boiling-point>
  <density nil="true"/>
  <solubility>Freely soluble (maleate salt)</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure>Antihistamines are well absorbed from the gastrointestinal tract after oral administration.</route-of-exposure>
  <target nil="true"/>
  <mechanism-of-toxicity>Brompheniramine works by acting as an antagonist of the H1 histamine receptors. It also functions as a moderately effective anticholingeric agent, likely an antimuscarinic agent similar to other common antihistamines such as diphenhydramine. Its effects on the cholinergic system may include side-effects such as drowsiness, sedation, dry mouth, dry throat, blurred vision, and increased heart rate.</mechanism-of-toxicity>
  <metabolism>Hepatic (cytochrome P-450 system), some renal.</metabolism>
  <toxicity>Oral, Rat: LD&lt;sub&gt;50&lt;/sub&gt; = 318 mg/kg.</toxicity>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>For the treatment of the symptoms of the common cold and allergic rhinitis, such as runny nose, itchy eyes, watery eyes, and sneezing.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms>Signs of overdose include fast or irregular heartbeat, mental or mood changes, tightness in the chest, and unusual tiredness or weakness.</symptoms>
  <treatment nil="true"/>
  <created-at type="dateTime">2014-08-30T21:03:45Z</created-at>
  <updated-at type="dateTime">2014-12-24T20:26:52Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Brompheniramine</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C06857</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>3183</chebi-id>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB00835</drugbank-id>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CN(C)CCC(C1=CC=C(Br)C=C1)C1=CC=CC=N1</moldb-smiles>
  <moldb-formula>C16H19BrN2</moldb-formula>
  <moldb-inchi>InChI=1/C16H19BrN2/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13/h3-9,11,15H,10,12H2,1-2H3</moldb-inchi>
  <moldb-inchikey>InChIKey=ZDIGNSYAACHWNL-UHFFFAOYNA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">319.239</moldb-average-mass>
  <moldb-mono-mass type="decimal">318.073161265</moldb-mono-mass>
  <origin>Exogenous</origin>
  <state>Liquid</state>
  <logp>3.4</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id>6573</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>&lt;p&gt;Sperber, N., Papa, D. and Schwenk, E.; US. Patent 2,567,245; September 11, 1951; assigned&lt;br /&gt;
to Schering Corporation.&lt;br /&gt;
Sperber, N., Papa, D. and Schwenk, E.; U.S. Patent 2,676,964: April 27,1954; assigned to&lt;br /&gt;
Schering Corporation.&lt;/p&gt;</synthesis-reference>
  <structure-image-caption nil="true"/>
</compound>
