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A comprehensive review of multi-target directed ligands in the treatment of Alzheimer's disease.
Pathak, Chandni; Kabra, Uma D.
Affiliation
  • Pathak C; Department of Pharmaceutical Chemistry, Parul Institute of Pharmacy, Parul University, Vadodara, Gujarat, India.
  • Kabra UD; Department of Pharmaceutical Chemistry, Parul Institute of Pharmacy, Parul University, Vadodara, Gujarat, India. Electronic address: uma.kabra16205@paruluniversity.ac.in.
Bioorg Chem ; 144: 107152, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38290187
ABSTRACT
Alzheimer's disease (AD) is the most common form of dementia affecting specifically older population. AD is an irreversible neurodegenerative CNS disorder associated with complex pathophysiology. Presently, the USFDA has approved only four drugs viz. Donepezil, Rivastigmine, Memantine, and Galantamine for the treatment of AD. These drugs exhibit their neuroprotective effects either by inhibiting cholinesterase enzyme (ChE) or N-methyl-d-aspartate (NMDA) receptor. However, the conventional therapy "one target, one molecule" has failed to provide promising therapeutic effects due to the multifactorial nature of AD. This triggered the development of a novel strategy called Multi-Target Directed Ligand (MTDL) which involved designing one molecule that acts on multiple targets simultaneously. The present review discusses the detailed pathology involved in AD and the various MTDL design strategies bearing different heterocycles, in vitro and in vivo activities of the compounds, and their corresponding structure-activity relationships. This knowledge will allow us to identify and design more effective MTDLs for the treatment of AD.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alzheimer Disease Limits: Humans Language: En Journal: Bioorg Chem / Bioorganic chem / Bioorganic chemistry Year: 2024 Document type: Article Affiliation country: India Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alzheimer Disease Limits: Humans Language: En Journal: Bioorg Chem / Bioorganic chem / Bioorganic chemistry Year: 2024 Document type: Article Affiliation country: India Country of publication: Estados Unidos