Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Lafutidine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Lafutidine
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
Identifiers
  • 2-(furan-2-ylmethylsulfinyl)-N-[(Z)-4-[4-(piperidin-1-ylmethyl)pyridin-2-yl]oxybut-2-enyl]acetamide
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
ECHA InfoCard100.118.935Edit this at Wikidata
Chemical and physical data
FormulaC22H29N3O4S
Molar mass431.55 g·mol−1
3D model (JSmol)
  • C1CCCCN1Cc2ccnc(c2)OC/C=C\CNC(=O)CS(=O)Cc3ccco3
  • InChI=1S/C22H29N3O4S/c26-21(18-30(27)17-20-7-6-14-28-20)23-9-2-5-13-29-22-15-19(8-10-24-22)16-25-11-3-1-4-12-25/h2,5-8,10,14-15H,1,3-4,9,11-13,16-18H2,(H,23,26)/b5-2- ☒N
  • Key:KMZQAVXSMUKBPD-DJWKRKHSSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Lafutidine (INN) is a second generationhistamine H2 receptor antagonist having multimodal mechanism of action and used to treatgastrointestinal disorders.[1] It is marketed in South Korea, Japan and India.

Medical use

[edit]

Lafutidine is used to treatgastric ulcers,duodenal ulcers, as well as wounds in the lining of the stomach associated with acutegastritis and acute exacerbation of chronic gastritis.[2][3]

Adverse effects

[edit]

Adverse events observed during clinical trials includedconstipation,diarrhea, drugrash,nausea,vomiting anddizziness.[3]

Mechanism of action

[edit]

Like otherH2 receptor antagonists, lafutidineacts by preventing the secretion ofgastric acid.[3] It also activatescalcitonin gene-related peptide, resulting in the stimulation ofnitric oxide (NO) and regulation of gastric mucosal blood flow, increasessomatostatin levels also resulting in less gastric acid secretion, causes the stomach lining to generate moremucin, inhibitsneutrophil activation thus preventing injury frominflammation, and blocks the attachment ofHelicobacter pylori to gastric cells.[3]

Trade names

[edit]

It is marketed in Japan asStogar byUCB[2] and in India asLafaxid by Zuventus Healthcare.[3] It is also marketed in South Korea asIldong Lafutidine by Ildong Pharmaceutical Co Ltd.

References

[edit]
  1. ^Tanaka M, Banba M, Joko A, Moriyama Y (June 2001)."[Pharmacological and therapeutic properties of lafutidine (stogar and protecadin), a novel histamine H2 receptor antagonist with gastroprotective activity]".Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica (in Japanese).117 (6):377–86.doi:10.1254/fpj.117.377.PMID 11436515.
  2. ^abUCB Japan Revised: April 2005Stogar tabletsArchived 2014-11-29 at theWayback Machine
  3. ^abcdeZuventus Healthcare Ltd. IndiaLafaxid tablets
H2 antagonists ("-tidine")
Prostaglandins (E)/
analogues ("-prost-")
Proton-pump inhibitors
("-prazole")
Potassium-competitive
acid blockers
("-prazan")
Others
Combinations
H1
Agonists
Antagonists
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists
Retrieved from "https://en.wikipedia.org/w/index.php?title=Lafutidine&oldid=1295588594"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp