| Publication Type |
Journal Article |
| Title |
New Tacrine Hybrids with Natural-Based Cysteine Derivatives as Multitargeted Drugs for Potential Treatment of Alzheimer s Disease |
| Authors |
Rangappa S. Keri Catarina Quintanova Sílvia Chaves Diana F. Silva Sandra M. Cardoso M. Amélia Santos |
| Groups |
BIOIN |
| Journal |
CHEMICAL BIOLOGY \& DRUG DESIGN |
| Year |
2016 |
| Month |
January |
| Volume |
87 |
| Number |
1 |
| Pages |
101-111 |
| Abstract |
Alzheimer s disease (AD) is a devastating age-dependent neurodegenerative disorder. The main hallmarks are impairment of cholinergic system and accumulation in brain of beta-amyloid (A beta) aggregates, which have been associated with oxidative damage and dyshomeostasis of redox-active biometals. The absence of an efficient treatment that could delay or cure AD has been attributed to the complexity and multifactorial nature of this disease. With this in mind and the recent interest on natural-based drugs, we have explored a set of natural-based hybrid compounds by conjugation of a tacrine moiety with an S-allylcysteine (garlic constituent) or S-propargylcysteine moiety aimed at improving the cholinergic system and neuroprotective capacity. The docking modeling studies allowed the selection of linkers to optimize the bimodal drug interaction with acetylcholinesterase enzyme (AChE) active site. The compounds were evaluated for some representative biological properties, including AChE activity and A beta aggregation inhibition, as well as for their neuroprotective activity to A beta- and ROS-induced cellular toxicity. The most promising results were achieved by compounds 9d for the AChE inhibition and 9l for the remarkable prevention of superoxide production and A beta-induced cellular toxicity. |
| DOI |
http://dx.doi.org/10.1111/cbdd.12633 |
| ISBN |
|
| Publisher |
WILEY-BLACKWELL |
| Book Title |
|
| ISSN |
1747-0277 |
| EISSN |
1747-0285 |
| Conference Name |
|
| Bibtex ID |
ISI:000368011000008 |
| Observations |
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