Phenothiazine‐based chalcones as potential dual‐target inhibitors toward cholinesterases (AChE, BuChE) and monoamine oxidases (MAO‐A, MAO‐B)-Reference-Cited by-同舟云学术

Phenothiazine‐based chalcones as potential dual‐target inhibitors toward cholinesterases (AChE, BuChE) and monoamine oxidases (MAO‐A, MAO‐B)

Published:2020-10-16 Issue:1 Volume:58 Page:161-171
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J Heterocyclic Chem

Author:

Yamali Cem¹²^ORCID,Engin Feyza Sena¹,Bilginer Sinan¹,Tugrak Mehtap¹^ORCID,Ozmen Ozgun Dilan³,Ozli Gulsen⁴,Levent Serkan⁵,Saglik Begum Nurpelin⁵,Ozkay Yusuf⁵^ORCID,Gul Halise Inci¹

Affiliation:

1. Department of Pharmaceutical Chemistry, Faculty of Pharmacy Ataturk University Erzurum Turkey

2. Department of Basic Pharmaceutical Sciences, Faculty of Pharmacy Cukurova University Adana Turkey

3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy Agri Ibrahim Cecen University Agri Turkey

4. Department of Pharmaceutical Chemistry, Faculty of Pharmacy Erzincan University Erzincan Turkey

5. Department of Pharmaceutical Chemistry, Faculty of Pharmacy Anadolu University Eskisehir Turkey

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4156

Reference40 articles.

1. Conjugates of γ-Carbolines and Phenothiazine as new selective inhibitors of butyrylcholinesterase and blockers of NMDA receptors for Alzheimer Disease

2. A Focused Library of Psychotropic Analogues with Neuroprotective and Neuroregenerative Potential

3. Design, synthesis, in-silico and biological evaluation of novel chalcone derivatives as multi-function agents for the treatment of Alzheimer's disease

4. Effects of phenothiazine-structured compounds on APP processing in Alzheimer's disease cellular model

5. Selective reversible inhibition of human butyrylcholinesterase by aryl amide derivatives of phenothiazine

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