Cardanol-derived AChE inhibitors: Towards the development of dual binding derivatives for Alzheimer's disease
Language English Country France Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
PubMed
26735910
DOI
10.1016/j.ejmech.2015.12.024
PII: S0223-5234(15)30412-8
Knihovny.cz E-resources
- Keywords
- Acetylcholinesterase, Alzheimer's disease, Cashew nut shell liquid, Dual binding site AChE inhibitors, Multitarget compounds,
- MeSH
- Alzheimer Disease drug therapy enzymology MeSH
- HT29 Cells MeSH
- Cholinesterase Inhibitors chemical synthesis chemistry pharmacology MeSH
- Cholinesterases metabolism MeSH
- Phenols chemical synthesis chemistry pharmacology MeSH
- Humans MeSH
- Molecular Structure MeSH
- Binding Sites drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- cardanol MeSH Browser
- Cholinesterase Inhibitors MeSH
- Cholinesterases MeSH
- Phenols MeSH
Cardanol is a phenolic lipid component of cashew nut shell liquid (CNSL), obtained as the byproduct of cashew nut food processing. Being a waste product, it has attracted much attention as a precursor for the production of high-value chemicals, including drugs. On the basis of these findings and in connection with our previous studies on cardanol derivatives as acetylcholinesterase (AChE) inhibitors, we designed a novel series of analogues by including a protonable amino moiety belonging to different systems. Properly addressed docking studies suggested that the proposed structural modifications would allow the new molecules to interact with both the catalytic active site (CAS) and the peripheral anionic site (PAS) of AChE, thus being able to act as dual binding inhibitors. To disclose whether the new molecules showed the desired profile, they were first tested for their cholinesterase inhibitory activity towards EeAChE and eqBuChE. Compound 26, bearing an N-ethyl-N-(2-methoxybenzyl)amine moiety, showed the highest inhibitory activity against EeAChE, with a promising IC50 of 6.6 μM, and a similar inhibition profile of the human isoform (IC50 = 5.7 μM). As another positive feature, most of the derivatives did not show appreciable toxicity against HT-29 cells, up to a concentration of 100 μM, which indicates drug-conform behavior. Also, compound 26 is capable of crossing the blood-brain barrier (BBB), as predicted by a PAMPA-BBB assay. Collectively, the data suggest that the approach to obtain potential anti-Alzheimer drugs from CNSL is worth of further pursuit and development.
Department for Life Quality Studies University of Bologna Corso D'Augusto 237 47921 Rimini Italy
Department of Pharmacy and Biotechnology University of Bologna Via Belmeloro 6 40126 Bologna Italy
References provided by Crossref.org
Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer's Disease
Novel Sustainable-by-Design HDAC Inhibitors for the Treatment of Alzheimer's Disease
Profiling donepezil template into multipotent hybrids with antioxidant properties
Development of 2-Methoxyhuprine as Novel Lead for Alzheimer's Disease Therapy