Abstract

Three new ent-kaurane diterpenoids, namely annoglabrin A-C (1-3), were isolated from the Annona glabra fruit pulp. Their structures were clarified by widespread spectroscopic analyses (1D and 2D NMR, HRESIMS). The relative configuration of these new compounds was established through the NOESY spectrum. Compounds 1-3 were evaluated for their inhibitory activity against α-glucosidase and were found with weak (1 and 3) or no effects (2), compared to those of positive control (acarbose, IC50 82.0 µM).

Keywords:
Two-dimensional nuclear magnetic resonance spectroscopy Pulp (tooth) Terpenoid Nuclear magnetic resonance spectroscopy

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Topics

Traditional and Medicinal Uses of Annonaceae
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Biochemistry
Phytochemicals and Antioxidant Activities
Health Sciences →  Medicine →  Biochemistry
Natural Compound Pharmacology Studies
Life Sciences →  Agricultural and Biological Sciences →  Plant Science
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