Methapyrilene

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
"Thionylan" redirects here. The thionyl halides should not be confused with "thionylan" and include thionyl fluoride, thionyl chloride, and thionyl bromide.
Methapyrilene
Methapyrilene.svg
Systematic (IUPAC) name
N,N-dimethyl-N'-pyridin-2-yl-N'-(2-thienylmethyl)ethane-1,2-diamine
Identifiers
CAS Number 91-80-5 YesY
ATC code R06AC05 (WHO)
PubChem CID: 4098
DrugBank DB04819 YesY
ChemSpider 3956 YesY
UNII A01LX40298 YesY
KEGG C11114 YesY
ChEBI CHEBI:6820 YesY
Chemical data
Formula C14H19N3S
Molecular mass 261.387 g/mol
  • n1ccccc1N(CCN(C)C)Cc2sccc2
  • InChI=1S/C14H19N3S/c1-16(2)9-10-17(12-13-6-5-11-18-13)14-7-3-4-8-15-14/h3-8,11H,9-10,12H2,1-2H3 YesY
  • Key:HNJJXZKZRAWDPF-UHFFFAOYSA-N YesY
  (verify)

Methapyrilene is an antihistamine and anticholinergic of the pyridine chemical class which was developed in the early 1950s. It was sold under the trade names Co-Pyronil and Histadyl EC.[1] It has relatively strong sedative effects, to the extent that its primary use was as a medication for insomnia rather than for its antihistamine action. Together with scopolamine, it was the main ingredient in Sominex, Nytol, and Sleep-Eze. It also provided the sedative component of Excedrin PM. All of these products were reformulated in the late 1970s when methapyrilene was demonstrated to cause liver cancer in rats when given chronically.[2]

See also

References

  1. The Birmingham Post Archive. thefreelibrary.com
  2. Lua error in package.lua at line 80: module 'strict' not found.


<templatestyles src="Asbox/styles.css"></templatestyles>

<templatestyles src="Asbox/styles.css"></templatestyles>