Multifunctional hybrid sulfonamides as novel therapeutic agents for Alzheimer's disease

Aim: A breakthrough in modern medicine, in terms of treatment of Alzheimer's disease, is yet to be seen, as the scene is currently plagued with numerous clinical trial failures. Here, we are exploring multifunctional hybrid sulfonamides for their anti-Alzheimer activity due to the complex nature of the disease. Results & methodology: Compound 41 showed significant inhibition of MMP-2 (IC50: 18.24 ± 1.62 nM), AChE (IC50: 4.28 ± 0.15 μM) and BuChE (IC50: 1.32 ± 0.02 μM). It also exhibited a metal-chelating property, as validated by an in vitro metal-induced Aβ aggregation assay using confocal fluorescence imaging. Whereas, MTT and DPPH assays revealed it to be nontoxic and neuroprotective with substantial antioxidant property. Conclusion: The present study puts forth potent yet nontoxic lead molecules, which foray into the field of multitargeted agents for the treatment of Alzheimer's disease.

Medienart:

E-Artikel

Erscheinungsjahr:

2019

Erschienen:

2019

Enthalten in:

Zur Gesamtaufnahme - volume:11

Enthalten in:

Future medicinal chemistry - 11(2019), 24 vom: 21. Dez., Seite 3161-3178

Sprache:

Englisch

Beteiligte Personen:

Swetha, Rayala [VerfasserIn]
Kumar, Devendra [VerfasserIn]
Gupta, Sukesh K [VerfasserIn]
Ganeshpurkar, Ankit [VerfasserIn]
Singh, Ravi [VerfasserIn]
Gutti, Gopichand [VerfasserIn]
Kumar, Dileep [VerfasserIn]
Jana, Srabanti [VerfasserIn]
Krishnamurthy, Sairam [VerfasserIn]
Singh, Sushil K [VerfasserIn]

Links:

Volltext

Themen:

β-alanine
Acetylcholine esterase
Acetylcholinesterase
Alzheimer’s disease
Amyloid β
Amyloid beta-Peptides
Butyrylcholinesterase
Chelating Agents
Cholinesterase Inhibitors
Confocal fluorescence microscopy
EC 3.1.1.7
EC 3.1.1.8
EC 3.4.24.24
Journal Article
MMP2 protein, human
Matrix Metalloproteinase 2
Matrix Metalloproteinase Inhibitors
Matrix metalloproteinase-2
Metal chelation
Research Support, Non-U.S. Gov't
Sulfonamides

Anmerkungen:

Date Completed 10.07.2020

Date Revised 10.07.2020

published: Print

Citation Status MEDLINE

doi:

10.4155/fmc-2019-0106

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM304399639