New Benzo[h][1,6]naphthyridine and Azepino[3,2-c]quinoline Derivatives as Selective Antagonists of 5-HT4 Receptors:  Binding Profile and Pharmacological …

A Hinschberger, S Butt, V Lelong… - Journal of medicinal …, 2003 - ACS Publications
A series of benzo [h][1, 6] naphthyridine and azepino [3, 2-c] quinoline derivatives were
prepared and evaluated to determine the necessary requirements for high affinity on the 5 …

5-HT3 Receptor antagonists. 2. 4-Hydroxy-4-quinolinecarboxylic acid derivatives

H Hayashi, Y Miwa, S Ichikawa, N Yoda… - Journal of medicinal …, 1993 - ACS Publications
A series of 4-hydroxy-3-quinolinecarboxylic acid derivatives (6) and 4-hydroxy-2-oxo-1, 2-
dihydro-3-quinolinecarboxylic acid derivatives (7) were designed and synthesized as 5-HT3 …

[HTML][HTML] Evidence for a role of 5-HT1A receptor on antinociceptive action from Geissospermum vellosii

JAT Werner, SM Oliveira, DF Martins… - Journal of …, 2009 - Elsevier
ETHNOPHARMACOLOGICAL RELEVANCE: Geissospermum vellosii is a tree widely found
throughout the Amazonic forest and frequently used by the native population for painful …

1-[4-(3-Phenylalkyl)phenyl]-2-aminopropanes as 5-HT2A Partial Agonists

CS Dowd, K Herrick-Davis, C Egan… - Journal of medicinal …, 2000 - ACS Publications
Phenylalkylamines such as 1-(4-bromo-2, 5-dimethoxyphenyl)-2-aminopropane (DOB; 1a)
and its corresponding iodo derivative DOI (2) are commonly used 5-HT2 serotonin agonists …

Binding of STW 5 (Iberogast®) and its components to intestinal 5-HT, muscarinic M3, and opioid receptors

U Simmen, O Kelber, SN Okpanyi, R Jaeggi, B Bueter… - Phytomedicine, 2006 - Elsevier
Clinical studies with the fixed herbal combination product STW 5 (Iberogast®) have
indicated an efficacy comparable to metoclopramide (5-HT3 antagonist) and cisapride (5 …

Pharmacological properties and discriminative stimulus effects of a novel and selective 5-HT2 receptor agonist AL-38022A [(S)-2-(8, 9-dihydro-7H-pyrano [2, 3-g] …

JA May, NA Sharif, HH Chen, JC Liao, CR Kelly… - Pharmacology …, 2009 - Elsevier
AL-38022A is a novel synthetic serotonergic (5-HT) ligand that exhibited high affinity for
each of the 5-HT2 receptor subtypes (Ki≤ 2.2 nM), but a significantly lower (> 100-fold less) …

A Novel, Potent, and Selective 5-HT7 Antagonist:  (R)-3-(2-(2-(4-Methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl)phenol (SB-269970)

PJ Lovell, SM Bromidge, S Dabbs… - Journal of medicinal …, 2000 - ACS Publications
Introduction. The human 5-HT7 receptor is a recently discovered member of the seven-
transmembrane G-protein-coupled receptor superfamily. 2 The most abundant isoform 5 …

Indolebutylamines as Selective 5-HT1A Agonists

T Heinrich, H Böttcher, GD Bartoszyk… - Journal of medicinal …, 2004 - ACS Publications
A series of new 1-[4-(indol-3-yl) butyl]-4-arylpiperazines was prepared to identify highly
selective and potent 5-HT1A agonists as potential pharmacological tools in studies of mood …

Arylpiperazines with N-acylated amino acids as 5-HT1A receptor ligands

P Zajdel, G Subra, AJ Bojarski, B Duszyńska… - Bioorganic & medicinal …, 2006 - Elsevier
A library consisting of 60 arylpiperazines modified with N-acylated amino acids was
prepared on BAL linker SynPhase™ Lanterns and evaluated in vitro for 5-HT1A receptor …

Indoloxypropanolamine analogues as 5-HT1A receptor antagonists

JH Krushinski Jr, JM Schaus, DC Thompson… - Bioorganic & medicinal …, 2007 - Elsevier
Analogues of pindolol, 1-(1H-indol-4-yloxy)-3-isopropylamino-propan-2-ol, were
synthesized and evaluated as 5-HT1A receptor antagonists. The structural features required …