Perspective Design of Chalcones for the Management of CNS Disorders: A Mini-Review.

Chalcones GABA receptors acetylcholinesterase (AChE) anti-Alzheimer’s agents anti-depressant activity anxiolytic activity butyrylcholinesterase (BChE) inhibitions monoamine oxidase inhibition β-amyloid plaques imaging agents.

Journal

CNS & neurological disorders drug targets
ISSN: 1996-3181
Titre abrégé: CNS Neurol Disord Drug Targets
Pays: United Arab Emirates
ID NLM: 101269155

Informations de publication

Date de publication:
2019
Historique:
received: 19 03 2019
revised: 09 04 2019
accepted: 24 04 2019
pubmed: 13 6 2019
medline: 25 9 2020
entrez: 13 6 2019
Statut: ppublish

Résumé

The development of chalcone-based compounds for CNS disorders has been explored by many research groups. Chalcones are being considered as a potent organic scaffold with widespread applications in the field of drug discovery and medicinal chemistry. The planar or semi-planar geometry of chalcones with various functionalities impinged on the terminal aromatic systems renders the molecule its bio-activity including anti-cancer, anti-malarial, anti-microbial, anti-fungal, antileishmanial, anti-viral, anti-diabetic, anti-hypertensive properties, etc. Moreover, cutting-edge research has been executed in the domain of Central Nervous System (CNS) based scheme, further, their identification and classifications also remain of high interest in the field of medicinal chemistry but the specific reviews are limited. Hence, the present review highlights the significance of chalcones toward their CNS activities (up to 2019), which include anti-depressant activity, anxiolytic activity, activity with GABA receptors, acetylcholinesterase (AChE) and butyryl cholinesterase (BChE) inhibitions, activity as adenosine receptor antagonists anti-Alzheimer's agents, β-amyloid plaques imaging agents, monoamine oxidase inhibition. To our knowledge, this is the first review exclusively for CNS activity profile of chalcones.

Identifiants

pubmed: 31187716
pii: CNSNDDT-EPUB-98725
doi: 10.2174/1871527318666190610111246
doi:

Substances chimiques

Amyloid beta-Peptides 0
Chalcones 0
Cholinesterase Inhibitors 0
Monoamine Oxidase Inhibitors 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

432-445

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Bijo Mathew (B)

Division of Drug Design and Medicinal Chemistry Research Lab, Department of Pharmaceutical Chemistry, Ahalia School of Pharmacy, Palakkad 678557, Kerala, India.

Della Grace Thomas Parambi (DGT)

Department of Pharmaceutical Chemistry, Jouf University, Sakaka, Al Jouf, 2014, Saudi Arabia.

Vishnu Sankar Sivasankarapillai (VS)

Department of Chemistry, NSS Hindu College, Changanacherry, Kerala, 686103, India.

Md Sahab Uddin (MS)

Department of Pharmacy, Southeast University, Dhaka, Bangladesh.
Pharmakon Neuroscience Research Network, Dhaka, Bangladesh.

Jerad Suresh (J)

Department of Pharmaceutical Chemistry, College of Pharmacy, Madras Medical College, Chennai 600004, India.

Githa Elizabeth Mathew (GE)

Department of Pharmacology, Grace College of Pharmacy, Palakkad 678004, Kerala, India.

Monu Joy (M)

School of Pure & Applied Physics, M.G. University, Kottayam 686560, India.

Akash Marathakam (A)

Department of Pharmaceutical Chemistry, National College of Pharmacy, Calicut 673602, Kerala, India.

Sheeba Varghese Gupta (SV)

Department of Pharmaceutical Sciences, College of Pharmacy, University of South Florida, Tampa, FL 33612, United States.

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