Structure‐Activity Relationship Studies of CNS Agents, Part 23[1]): N‐(3‐Phenylpropyl)‐ and N‐[3(E)‐Cinnamyl]‐1,2,3,4‐tetrahydroisoquinoline Mimic 1‐Phenylpiperazine at 5 …

JL Mokrosz, AJ Bojarski… - Archiv der …, 1995 - Wiley Online Library
The 5‐HT1A receptor affinities and ionization constants of a set of 1‐arylpiperazine (4) 1, 2,
3, 4‐tetrahydroisoquinoline (6), and‐quinoline (7) containing N‐(ω‐arylalkyl) or N‐(E) …

Synthesis and pharmacology of isoquinuclidine derivatives as 5-HT3 ligands

I Iriepa, FJ Villasante, E Gálvez, L Labeaga… - Bioorganic & medicinal …, 2002 - Elsevier
A series of 4-amino-5-chloro-2-methoxybenzoates and benzamides containing the 5-and 6-
isoquinuclidinyl system was synthesised and evaluated for binding to 5-HT3, 5-HT4 and D2 …

Discovery of a series of (4, 5-dihydroimidazol-2-yl)-biphenylamine 5-HT7 agonists

V Parikh, WM Welch, AW Schmidt - Bioorganic & medicinal chemistry …, 2003 - Elsevier
A novel (4, 5-dihydroimidazol-2-yl)-biphenylamine series of 5-HT7 agonist compounds was
developed from a structurally related lead compound 1. The newly discovered series is …

Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands

M Paillet-Loilier, F Fabis, A Lepailleur, R Bureau… - Bioorganic & medicinal …, 2005 - Elsevier
Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands -
ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books Search …

Alkaloids from Tabernaemontana

B Danieli, G Palmisano - The alkaloids: Chemistry and pharmacology, 1986 - Elsevier
Publisher Summary This chapter discusses taxonomy, indole alkaloids from chemically
investigated Tabernaemontana species, structure elucidation and chemistry, and …

Triterpenoids from two Terminalia species

W Wang, Z Ali, XC Li, Y Shen, IA Khan - Planta medica, 2010 - thieme-connect.com
Phytochemical investigations of Terminalia arjuna bark and Terminalia chebula fruits
resulted in the isolation of twelve triterpenoids including two new oleanane type triterpene …

Efficacy of selective 5‐HT6 receptor ligands determined by monitoring 5‐HT6 receptor‐mediated cAMP signaling pathways

G Romero, E Sánchez, M Pujol, P Pérez… - British journal of …, 2006 - Wiley Online Library
1 Two novel selective 5‐HT6 receptor ligands E‐6801 (6‐chloro‐N‐(3‐(2‐(dimethylamino)
ethyl)‐1H‐indol‐5‐yl) imidazo [2, 1‐b] thiazole‐5‐sulfonamide) and E‐6837 (5‐chloro‐N‐(3 …

4-(2-Aminoethoxy)-N-(phenylsulfonyl) indoles as novel 5-HT6 receptor ligands

P Zhou, Y Yan, R Bernotas, BL Harrison… - Bioorganic & medicinal …, 2005 - Elsevier
The preparation of a novel class of 4-(2-aminoethoxy)-N-(phenylsulfonyl) indoles which
exhibit high affinity towards the 5-HT6 receptor is reported here. Among these compounds, 4 …

Bioactive constituents of Atriplex halimus plant.

SS Emam - 2011 - cabidigitallibrary.org
Chemical analysis of Atriplex halimus (Family: Chenopodiaceae) revealed that the plant at
Wadi-Hof and Wadi-Sudr habitats contained eleven free amino acids with different range of …

Skimmianine and related furoquinolines function as antagonists of 5‐hydroxytryptamine receptors in animals

JT Cheng, TK Chang, IS Chent - Journal of autonomic …, 1994 - Wiley Online Library
1 Skimmianine, kokusaginine and confusameline, three furoquinolines extracted from the
leaves of Evodia merrillii (Rutaceae), were investigated to characterize their selective effects …