Two new minor Amaryllidaceae alkaloids were isolated from × cv. Ferrari and cv. Carlton. The chemical structures were identified by various spectroscopic (one- and two-dimensional (1D and 2D) NMR, circular dichroism (CD), high-resolution mass spectrometry (HRMS) and by comparison with literature data of similar compounds. Both isolated alkaloids were screened for their human acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhibition activity. One of the new compounds, a heterodimer alkaloid of narcikachnine-type, named narciabduliine (), showed balanced inhibition potency for both studied enzymes, with IC values of 3.29 ± 0.73 µM for AChE and 3.44 ± 0.02 µM for BuChE. The accommodation of into the active sites of respective enzymes was predicted using molecular modeling simulation.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956344PMC
http://dx.doi.org/10.3390/molecules26051279DOI Listing

Publication Analysis

Top Keywords

inhibition activity
8
minor amaryllidaceae
8
amaryllidaceae alkaloids
8
structure elucidation
4
elucidation cholinesterase
4
cholinesterase inhibition
4
activity minor
4
alkaloids minor
4
alkaloids isolated
4
isolated ferrari
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!