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Recent advancements in chromone as a privileged scaffold towards the development of small molecules for neurodegenerative therapeutics.
Madhav, Hari; Jameel, Ehtesham; Rehan, Mohammad; Hoda, Nasimul.
Afiliación
  • Madhav H; Drug Design and Synthesis Laboratory, Department of Chemistry, Jamia Millia Islamia New Delhi 110025 India harimadhavgautam@gmail.com nhoda@jmi.ac.in.
  • Jameel E; College of Pharmaceutical Sciences, Zhejiang University Hangzhou PR China ehteshamjameel@zju.edu.cn.
  • Rehan M; Max-Planck-Institute für Molekulare Physiologie, Abteilung Chemische Biologie Otto-Hahn-Straße 11 44227 Dortmund Germany rehan.10aug@gmail.com.
  • Hoda N; Drug Design and Synthesis Laboratory, Department of Chemistry, Jamia Millia Islamia New Delhi 110025 India harimadhavgautam@gmail.com nhoda@jmi.ac.in.
RSC Med Chem ; 13(3): 258-279, 2022 Mar 23.
Article en En | MEDLINE | ID: mdl-35434628
ABSTRACT
Neurodegenerative disorders, i.e., Alzheimer's or Parkinson's disease, involve progressive degeneration of the central nervous system, resulting in memory loss and cognitive impairment. The intensification of neurodegenerative research in recent years put some molecules into clinical trials, but still there is an urgent need to develop effective therapeutic molecules to combat these diseases. Chromone is a well-identified privileged structure for the design of well-diversified therapeutic molecules of potential pharmacological interest, particularly in the field of neurodegeneration. In this short review, we focused on the recent advancements and developments of chromones for neurodegenerative therapeutics. Different small molecules were reviewed as multi-target-directed ligands (MTDLs) with potential inhibition of AChE, BuChE, MAO-A, MAO-B, Aß plaque formation and aggregation. Recently developed MTDLs emphasized that the chromone scaffold has the potential to develop new molecules for the treatment of neurodegenerative diseases.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Med Chem Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: RSC Med Chem Año: 2022 Tipo del documento: Article
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