serw-MX  [xml]  
 


    
 DeCS Categories

D02 Organic Chemicals .
D02.078 Amidines .
D02.078.370 Guanidines .
D02.078.370.200 Cimetidine .
D02.886 Sulfur Compounds .
D02.886.675 Thiazoles .
D02.886.675.215 Famotidine .
D02.886.675.500 Nizatidine .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.129 Azoles .
D03.383.129.308 Imidazoles .
D03.383.129.308.130 Cimetidine .
D03.383.129.708 Thiazoles .
D03.383.129.708.215 Famotidine .
D03.383.129.708.500 Nizatidine .
D27 Chemical Actions and Uses .
D27.505 Pharmacologic Actions .
D27.505.519 Molecular Mechanisms of Pharmacological Action .
D27.505.519.625 Neurotransmitter Agents .
D27.505.519.625.375 Histamine Agents .
D27.505.519.625.375.400 Histamine Agonists .
D27.505.519.625.375.425 Histamine Antagonists .
D27.505.519.625.375.425.425 Histamine H2 Antagonists .
D27.505.696 Physiological Effects of Drugs .
D27.505.696.577 Neurotransmitter Agents .
D27.505.696.577.375 Histamine Agents .
D27.505.696.577.375.400 Histamine Agonists .
D27.505.696.577.375.425 Histamine Antagonists .
D27.505.696.577.375.425.425 Histamine H2 Antagonists .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Famotidine .
Famotidine Hydrochloride .
MK-208 .
Pepcid .
YM-11170 .
MK 208 .
MK208 .
YM 11170 .
YM11170 .
A competitive histamine H2-receptor antagonist. Its main pharmacodynamic effect is the inhibition of gastric secretion. .
1.00
261551
 
Cimetidine .
Altramet .
Biomet .
Biomet400 .
Cimetidine HCl .
Cimetidine Hydrochloride .
Eureceptor .
Histodil .
N-Cyano-N'-methyl-N''-(2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)guanidine .
SK&F-92334 .
SKF-92334 .
Tagamet .
HCl, Cimetidine .
Hydrochloride, Cimetidine .
SK&F 92334 .
SK&F92334 .
SKF 92334 .
SKF92334 .
A histamine congener, it competitively inhibits HISTAMINE binding to HISTAMINE H2 RECEPTORS. Cimetidine has a range of pharmacological actions. It inhibits GASTRIC ACID secretion, as well as PEPSIN and GASTRIN output. .
0.45
1869162
 
Histamine H2 Antagonists .
Antagonists, Histamine H2 .
Blockaders, Histamine H2 Receptor .
H2 Receptor Blockaders .
Histamine H2 Blockers .
Receptor Antagonists, Histamine H2 .
Receptor Blockaders, H2 .
Blockaders, H2 Receptor .
Blockers, Histamine H2 .
H2 Antagonists, Histamine .
H2 Antihistaminics .
H2 Blockers, Histamine .
Antihistaminics, H2 .
Histamine H2 Receptor Antagonists .
Histamine H2 Receptor Blockaders .
Drugs that selectively bind to but do not activate histamine H2 receptors, thereby blocking the actions of histamine. Their clinically most important action is the inhibition of acid secretion in the treatment of gastrointestinal ulcers. Smooth muscle may also be affected. Some drugs in this class have strong effects in the central nervous system, but these actions are not well understood. .
0.43
996986
 
Nizatidine .
Axid 18090 .
LY-139037 .
N-(2-(((2-((Dimethylamino)methyl)-4-thiazolyl)methyl)thio)ethyl)-N'-methyl-2-nitro-1,1-ethenediamine .
LY 139037 .
LY139037 .
A histamine H2 receptor antagonist with low toxicity that inhibits gastric acid secretion. The drug is used for the treatment of duodenal ulcers. .
0.43
8311
 
Histamine Agonists .
H1 Agonist .
H1 Agonists .
H2 Agonist .
H2 Agonists .
H3 Agonist .
H3 Agonists .
Histamine Agonist .
Histamine H1 Agonist .
Histamine H1 Receptor Agonist .
Histamine H1 Receptor Agonists .
Histamine H2 Agonist .
Histamine H2 Receptor Agonist .
Histamine H2 Receptor Agonists .
Histamine H3 Agonist .
Histamine H3 Receptor Agonists .
Histaminergic Agonist .
Histaminergic Agonists .
Agonist, H1 .
Agonist, H2 .
Agonist, H3 .
Agonist, Histamine .
Agonist, Histamine H1 .
Agonist, Histamine H2 .
Agonist, Histamine H3 .
Agonist, Histaminergic .
Agonists, H1 .
Agonists, H2 .
Agonists, H3 .
Agonists, Histamine .
Agonists, Histamine H1 .
Agonists, Histamine H2 .
Agonists, Histamine H3 .
Agonists, Histaminergic .
H1 Agonist, Histamine .
H1 Agonists, Histamine .
H2 Agonist, Histamine .
H2 Agonists, Histamine .
H3 Agonist, Histamine .
H3 Agonists, Histamine .
Histamine H1 Agonists .
Histamine H2 Agonists .
Histamine H3 Agonists .
Drugs that bind to and activate histamine receptors. Although they have been suggested for a variety of clinical applications histamine agonists have so far been more widely used in research than therapeutically. .
0.38
111225