Octoclothepin enantiomers. A reinvestigation of their biochemical and pharmacological activity in relation to a new receptor-interaction model for dopamine D-2 receptor antagonists

1991 ◽  
Vol 34 (7) ◽  
pp. 2023-2030 ◽  
Author(s):  
Klaus P. Boegesoe ◽  
Tommy Liljefors ◽  
Joern Arnt ◽  
John Hyttel ◽  
Henrik Pedersen
2003 ◽  
Vol 13 (7) ◽  
pp. 1245-1248 ◽  
Author(s):  
Liantao Li ◽  
Julia Kracht ◽  
Shiqi Peng ◽  
Günther Bernhardt ◽  
Armin Buschauer

2021 ◽  
Vol 12 (1) ◽  
pp. 86
Author(s):  
Pilar Marcos ◽  
Rafael Coveñas

To know the processes involved in feeding, the dysregulation of hypothalamic neuropeptides promoting anorexigenic/orexigenic mechanisms must be investigated. Many neuropeptides are involved in this behavior and in overweight/obesity. Current pharmacological strategies for the treatment of obesity are unfortunately not very effective and, hence, new therapeutic strategies must be investigated and developed. Due to the crucial role played by orexins in feeding behavior, the aim of this review is to update the involvement of the orexinergic system in this behavior. The studies performed in experimental animal models and humans and the relationships between the orexinergic system and other substances are mentioned and discussed. Promising research lines on the orexinergic system are highlighted (signaling pathways, heterogeneity of the hypothalamic orexinergic neurons, receptor-receptor interaction, and sex differences). Each of the orexin 1 and 2 receptors plays a unique role in energy metabolism, exerting a differential function in obesity. Additional preclinical/clinical studies must be carried out to demonstrate the beneficial effects mediated by orexin receptor antagonists. Because therapies applied are in general ineffective when they are directed against a single target, the best option for successful anti-obesity treatments is the development of combination therapies as well as the development of new and more specific orexin receptor antagonists.


1995 ◽  
Vol 50 (9-10) ◽  
pp. 708-714
Author(s):  
V. Kettmann ◽  
J. Sivý

Abstract We report here a molecular modeling study of selected conformationally constrained phenylcarbamate local anesthetics in relation to the available pharmacological data that enabled us to develop a receptor-interaction model for this class of drugs. The validity of the model was confirmed on other semirigid analogues prepared for this study. The results suggest that the phenyl ring is most likely involved in a stacking interaction with a complementary receptor site and the tertiary ammonium group is capable of both hydrogen bonding and lipophilic interactions.


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