Chemistry & Biodiversity · 2016 · 40 citations · 29 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryNeuropharmacologyStructure-activity RelationshipsCholinergic NeurochemistryEnzyme InhibitionStructure-activity Relationship AnalysisAbsolute Configuration AssignmentAbsolute Configuration DeterminationCircular DichroismCircular Dichroism AnalysisIsoquinoline AlkaloidsIsoquinoline ChemistryPlant AlkaloidsQuinoline Alkaloids
Two new isoquinoline alkaloids, named fumaranine (2) and fumarostrejdine (10), along with 18 known alkaloids were isolated from aerial parts of Fumaria officinalis. The structures of the isolated compounds were elucidated on the basis of spectroscopic analyses and by comparison with literature data. The absolute configuration of the new compound 2 was determined by comparing its circular dichroism spectra with those of known analogs. Compounds isolated in sufficient amounts were evaluated for their acetylcholinesterase, butyrylcholinesterase, prolyl oligopeptidase (POP), and glycogen synthase kinase-3β inhibitory activities. Parfumidine (8) and sinactine (15) exhibited potent POP inhibition activities (IC50 99±5 and 53±2 μM, resp.).
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A new and rapid colorimetric determination of acetylcholinesterase activity
George L. Ellman, K. Diane Courtney, Valentino Andres et al. · Biochemical Pharmacology · 1961 · 26.9K citations
James A. Dale, Harry S. Mosher · Journal of the American Chemical Society · 1973 · 2.6K citations