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GT 2331

Known as: GT-2331 
 

Topic mentions per year

Topic mentions per year

1998-2006
01219982006

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2007
2007
An investigation of the absolute configuration of the potent histamine H3 receptor antagonist GT-2331 using vibrational circular dichroism.
GT-2331 [(+)-1] is one of the most potent members of a class of chiral drug substances used to regulate the synthesis and release… (More)
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2006
2006
Detailed pharmacological characterization of GT-2331 for the rat histamine H3 receptor.
Histamine H(3) receptor antagonists are potential therapeutic agents for cognitive dysfunction, epilepsy, hypersomnia and obesity… (More)
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2005
2005
G protein-dependent pharmacology of histamine H3 receptor ligands: evidence for heterogeneous active state receptor conformations.
Previously reported pharmacological studies using the imidazole-containing histamine H3 receptor ligands GT-2331 (Cipralisant… (More)
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2004
2004
An efficient multigram synthesis of the potent histamine H3 antagonist GT-2331 and the reassessment of the absolute configuration.
GT-2331 is a potent histamine H(3) antagonist which has entered clinical trials. Efficient multigram syntheses of this compound… (More)
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2003
2003
Two novel and selective nonimidazole H3 receptor antagonists A-304121 and A-317920: II. In vivo behavioral and neurophysiological characterization.
Pharmacological blockade of central histamine H3 receptors (H3Rs) enhances cognition in rodents and offers promise for the… (More)
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2002
2002
Effects of histamine H(3) receptor ligands GT-2331 and ciproxifan in a repeated acquisition avoidance response in the spontaneously hypertensive rat pup.
Histamine H(3) receptor antagonists have been proposed as potentially useful therapeutic agents for the treatment of several… (More)
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2002
2002
Differential in vivo effects of H3 receptor ligands in a new mouse dipsogenia model.
The selective H(3) receptor agonist (R)-alpha-methylhistamine [(R)-alpha-MeHA] stimulates drinking in the adult rat. In the… (More)
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1999
1999
Development of trans-2-[1H-imidazol-4-yl] cyclopropane derivatives as new high-affinity histamine H3 receptor ligands.
Previously, a novel series of 1H-4-substituted imidazole compounds were described as potent and selective histamine (HA) H3… (More)
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1998
1998
High antagonist potency of GT-2227 and GT-2331, new histamine H3 receptor antagonists, in two functional models.
GT-2227 (4-(6-cyclohexylhex-cis-3-enyl)imidazole) and GT-2331 ((1R,2R)-4-(2-(5,5-dimethylhex-1-ynyl)cyclopropyl)imidazole) were… (More)
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