4-Methylhistamine: Difference between revisions
CSV import |
CSV import |
||
| Line 26: | Line 26: | ||
{{stub}} | {{stub}} | ||
{{No image}} | {{No image}} | ||
<gallery> | |||
File:4-Methylhistamine.svg|4-Methylhistamine | |||
</gallery> | |||
Revision as of 06:09, 3 March 2025
4-Methylhistamine is a histamine derivative that has been studied for its potential use in the treatment of gastric ulcers and inflammation. It is a selective H2 receptor agonist, meaning it binds to and activates these receptors, which are found in the stomach lining. This activation stimulates the production of gastric acid, which can help to heal ulcers.
History
4-Methylhistamine was first synthesized in the 1970s as part of a series of histamine derivatives. It was found to have a high affinity for H2 receptors, making it a useful tool for studying these receptors and their role in the body.
Pharmacology
As a selective H2 receptor agonist, 4-Methylhistamine has the ability to bind to and activate these receptors. This can lead to an increase in gastric acid production, which can help to heal gastric ulcers. However, this increased acid production can also lead to heartburn and other gastrointestinal symptoms.
Clinical use
While 4-Methylhistamine has been studied for its potential use in the treatment of gastric ulcers and inflammation, it is not currently approved for use in humans. Further research is needed to determine its safety and efficacy.


