N1-arylsulfonyl-3-(1, 2, 3, 6-tetrahydropyridin-4-yl)-1H-indole derivatives are potent and selective 5-HT6 receptor antagonists

DC Cole, JW Ellingboe, WJ Lennox… - Bioorganic & medicinal …, 2005 - Elsevier
A series of N1-arylsulfonyl-3-(1, 2, 3, 6-tetrahydropyridin-4-yl) indole derivatives was
designed and synthesized. These compounds were shown to have high affinity for the 5 …

1, 2, 4-Benzothiadiazine derivatives as α1 and 5-HT1A receptor ligands

A Tait, A Luppi, S Franchini, E Preziosi… - Bioorganic & medicinal …, 2005 - Elsevier
A series of new 1, 2, 4-benzothiadiazine derivatives with an arylpiperazine mojety linked at
position 3 of the heterocyclic ring were synthesized and assessed for their pharmacological …

Epiminocyclohepta [b] indole analogs as 5-HT6 antagonists

AJ Henderson, PR Guzzo, A Ghosh, J Kaur… - Bioorganic & medicinal …, 2012 - Elsevier
A new series of epiminocyclohepta [b] indoles with potent 5-HT6 antagonist activity were
discovered and optimized using in vitro protocols. One compound from this series was …

Discovery of 5-Arylsulfonamido-3- (pyrrolidin-2-ylmethyl)-1H-indole Derivatives as Potent, Selective 5-HT6 Receptor Agonists and Antagonists

DC Cole, WJ Lennox, S Lombardi… - Journal of medicinal …, 2005 - ACS Publications
5-Arylsulfonylamido-3-(pyrrolidin-2-ylmethyl)-1 H-indoles have been identified as high-
affinity 5-HT6 receptor ligands. Within this class, several of the (R)-enantiomers were potent …

Identification of 4-methyl-1, 2, 3, 4, 10, 10a-hexahydropyrazino [1, 2-a] indoles as 5-HT2C receptor agonists

S Röver, DR Adams, A Bénardeau, JM Bentley… - Bioorganic & medicinal …, 2005 - Elsevier
Synthesis and evaluation of the activity of new 4-methyl-1, 2, 3, 4, 10, 10a-
hexahydropyrazino [1, 2-a] indoles as 5-HT2C receptor agonists are described …

A Novel Ergot Alkaloid as a 5-HT1A Inhibitor Produced by Dicyma sp.

MJ Vázquez, AM Roa, F Reyes, A Vega… - Journal of Medicinal …, 2003 - ACS Publications
In the course of a search for small-molecule inhibitors of 5-hydroxytryptamine receptors we
have identified a novel ergoline derivative (1) from the fungal culture of Dicyma sp. This …

5-HT3 receptor antagonists. 1. New quinoline derivatives

H Hayashi, Y Miwa, I Miki, S Ichikawa… - Journal of medicinal …, 1992 - ACS Publications
A series of esters and amides of l-alkyl-2-oxo-1, 2-dihydroquinoline-4-carboxylic acid or 2-
alkoxy-quinoline-4-carboxylic acid containing a basic azabicycloalkyl moiety has been …

[引用][C] High Affinity of SDZ HTF‐919 and Related Molecules for Calf and Human Caudate 5‐HT4 Receptors

D Hoyer, D Fehlmann, D Langenegger… - Annals of the New …, 1998 - Wiley Online Library
Both functional and radioligand binding studies indicate that 5‐HT 4 receptors are
expressed in the CNS of several species, including human brain. 1 In order to determine the …

Synthesis and pharmacological evaluation of benzamide derivatives as selective 5-HT4 receptor agonists

S Sonda, T Kawahara, K Katayama, N Sato… - Bioorganic & medicinal …, 2005 - Elsevier
It is thought that selective 5-HT4 receptor agonists—such as 4-amino-5-chloro-2-methoxy-N-
[1-(6-oxo-6-phenylhexyl) piperidin-4-ylmethyl] benzamide (2)—have the ability to enhance …

Discovery of eight alkaloids with D1 and D2 antagonist activity in leaves of Nelumbo nucifera Gaertn. Using FLIPR assays

H Zhou, T Hou, Z Gao, X Guo, C Wang, J Wang… - Journal of …, 2021 - Elsevier
Ethnopharmacological relevance Dopamine receptors are long-standing primary targets in
the treatment of mental diseases and there is growing evidence that suggests relationships …