41 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
1507209	7	Histamine H2-receptor agonists. Synthesis, in vitro pharmacology, and qualitative structure-activity relationships of substituted 4- and 5-(2-aminoethyl)thiazoles.	Vrije Universiteit
20409707	66	Chiral NG-acylated hetarylpropylguanidine-type histamine H2 receptor agonists do not show significant stereoselectivity.	University Of Regensburg
19317445	53	N(G)-acylated imidazolylpropylguanidines as potent histamine H4 receptor agonists: selectivity by variation of the N(G)-substituent.	University Of Regensburg
18976927	83	Synthesis and structure-activity relationships for biphenyl H3 receptor antagonists with moderate anti-cholinesterase activity.	Universit£
9548813	53	The selective 5-HT1B receptor inverse agonist 1'-methyl-5-[[2'-methyl-4'-(5-methyl-1,2, 4-oxadiazol-3-yl)biphenyl-4-yl]carbonyl]-2,3,6,7-tetrahydro- spiro[furo[2,3-f]indole-3,4'-piperidine] (SB-224289) potently blocks terminal 5-HT autoreceptor function both in vitro and in vivo.	Smithkline Beecham Pharmaceuticals
1613748	8	Iodoaminopotentidine and related compounds: a new class of ligands with high affinity and selectivity for the histamine H2 receptor.	Freie Universit£T Berlin
2931524	19	The histamine H2 receptor agonist impromidine: synthesis and structure-activity considerations.	TBA
6131129	10	Conformational requirements for histamine H2-receptor inhibitors: a structure-activity study of phenylene analogues related to cimetidine and tiotidine.	TBA
6121913	5	Inhibitors of gastric acid secretion: 3,4-diamino-1,2,5-thiadiazole 1-oxides and 1,1-dioxides as urea equivalents in a series of histamine H2-receptor antagonists.	TBA
22216892	66	The bivalent ligand approach leads to highly potent and selective acylguanidine-type histamine H2 receptor agonists.	University Of Regensburg
20875743	90	Discovery of {1-[4-(2-{hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl}-1H-benzimidazol-1-yl)piperidin-1-yl]cyclooctyl}methanol, systemically potent novel non-peptide agonist of nociceptin/orphanin FQ receptor as analgesic for the treatment of neuropathic pain: design, synthesis, and structure-activity rela	Pfizer
18950149	75	Acylguanidines as bioisosteres of guanidines: NG-acylated imidazolylpropylguanidines, a new class of histamine H2 receptor agonists.	University Of Regensburg
12672253	60	Novel nonimidazole histamine H3 receptor antagonists: 1-(4-(phenoxymethyl)benzyl)piperidines and related compounds.	Freie Universit£T Berlin
12190321	55	Influence of bulky substituents on histamine h(3) receptor agonist/antagonist properties.	Freie Universit£T Berlin
10447960	20	Development of predictive retention-activity relationship models of tricyclic antidepressants by micellar liquid chromatography.	Universidad De Valencia
7904648	3	Studies on antiulcer drugs. 7. 2-Guanidino-4-pyridylthiazoles as histamine H2-receptor antagonists with potent gastroprotective effects against nonsteroidal antiinflammatory drug-induced injury.	Fujisawa Pharmaceutical
20812727	157	Synthesis, structure-affinity relationships, and radiolabeling of selective high-affinity 5-HT4 receptor ligands as prospective imaging probes for positron emission tomography.	National Institute Of Mental Health
16730977	2	Synthesis and pharmacological characterization of novel fluorescent histamine H2-receptor ligands derived from aminopotentidine.	The University Of Kansas
15115409	72	4-(omega-(alkyloxy)alkyl)-1H-imidazole derivatives as histamine H(3) receptor antagonists/agonists.	Freie UniversitäT Berlin
11855993	91	Development of a new class of nonimidazole histamine H(3) receptor ligands with combined inhibitory histamine N-methyltransferase activity.	Freie UniversitäT Berlin
10966752	60	New histamine H(3)-receptor ligands of the proxifan series: imoproxifan and other selective antagonists with high oral in vivo potency.	Freie UniversitäT Berlin
8676353	140	Novel carbamates as potent histamine H3 receptor antagonists with high in vitro and oral in vivo activity.	Freie UniversitäT Berlin
6192241	15	Synthesis and biological properties of thiophene ring analogues of mianserin.	TBA