Zhu_2023_Eur.J.Med.Chem_256_115414

Reference

Title : Aporphines: A privileged scaffold in CNS drug discovery - Zhu_2023_Eur.J.Med.Chem_256_115414
Author(s) : Zhu R , Jiang G , Tang W , Zhao X , Chen F , Zhang X , Ye N
Ref : Eur Journal of Medicinal Chemistry , 256 :115414 , 2023
Abstract :

Aporphine alkaloids embedded in 4H-dibenzo[de,g]quinoline four-ring structures belong to one of the largest subclasses of isoquinoline alkaloids. Aporphine is a privileged scaffold in the field of organic synthesis and medicinal chemistry for the discovery of new therapeutic agents for central nervous system (CNS) diseases, cancer, metabolic syndrome, and other diseases. In the past few decades, aporphine has attracted continuing interest to be widely used to develop selective or multitarget directed ligands (MTDLs) targeting the CNS (e.g., dopamine D(1/2/5), serotonin 5-HT(1A/2A/2C) and 5-HT(7), adrenergic alpha/beta receptors, and cholinesterase enzymes), thereby serving as valuable pharmacological probes for mechanism studies or as potential leads for CNS drug discovery. The aims of the present review are to highlight the diverse CNS activities of aporphines, discuss their SAR, and briefly summarize general synthetic routes, which will pave the way for the design and development of new aporphine derivatives as promising CNS active drugs in the future.

PubMedSearch : Zhu_2023_Eur.J.Med.Chem_256_115414
PubMedID: 37172474

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Citations formats

Zhu R, Jiang G, Tang W, Zhao X, Chen F, Zhang X, Ye N (2023)
Aporphines: A privileged scaffold in CNS drug discovery
Eur Journal of Medicinal Chemistry 256 :115414

Zhu R, Jiang G, Tang W, Zhao X, Chen F, Zhang X, Ye N (2023)
Eur Journal of Medicinal Chemistry 256 :115414