Methapyrilene
- "Thionylan" redirects here. The thionyl halides should not be confused with "thionylan" and include thionyl fluoride, thionyl chloride, and thionyl bromide.
Clinical data | |
---|---|
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C14H19N3S |
Molar mass | 261.387 g/mol |
3D model (JSmol) | |
| |
| |
(verify) |
WikiDoc Resources for Methapyrilene |
Articles |
---|
Most recent articles on Methapyrilene Most cited articles on Methapyrilene |
Media |
Powerpoint slides on Methapyrilene |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Methapyrilene at Clinical Trials.gov Trial results on Methapyrilene Clinical Trials on Methapyrilene at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Methapyrilene NICE Guidance on Methapyrilene
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Methapyrilene Discussion groups on Methapyrilene Patient Handouts on Methapyrilene Directions to Hospitals Treating Methapyrilene Risk calculators and risk factors for Methapyrilene
|
Healthcare Provider Resources |
Causes & Risk Factors for Methapyrilene |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
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]
Synthesis
See also
References
- ↑ The Birmingham Post Archive. thefreelibrary.com
- ↑ Lijinsky, W; Reuber, M.; Blackwell, B. (1980). "Liver tumors induced in rats by oral administration of the antihistaminic methapyrilene hydrochloride". Science. 209 (4458): 817–819. doi:10.1126/science.7403848. PMID 7403848.
- ↑ Leonard, Frederick; Solmssen, Ulrich V. (1948). "2-Thenyl Substituted Diamines with Antihistaminic Activity". Journal of the American Chemical Society. 70 (6): 2064–2067. doi:10.1021/ja01186a023.