A water extract of the leaves of Suregada glomerulata (Euphorbiaceae) was found to inhibit rat small intestinal α-glucosidase. An examination of the extract afforded 20 iminosugars including one pyrrolidine and 19 piperidines. The structures of the 10 new compounds (11-20) were determined by NMR, and MS spectroscopic data analyses, and chemical correlations. The novelty of the identified compounds mainly stems from the loss of a hydroxy at C-4 and the presence of an 8-hydroxyoctyl side chain. Nine N-alkyl derivatives including N-methyl (1a, 8a, and 13a), N-butyl (1b, 2b, and 9b) and N,N-dimethyl (1c, 2c, and 9c) were synthesized. The compounds were tested for rat small intestinal α-glucosidase inhibitory activity. In total, 15 compounds, including compounds 11, 12, 15, and 19 and the three derivatives 8a, 9b, and 13a, showed inhibitory activity with IC50 values less than 40μM. In vivo results showed that total alkaloids of S. glomerulata (10mg/kg) and four major iminosugars 1, 2, 3, and 9 (10mg/kg) can lower the postprandial blood glucose level after sucrose and starch load in healthy male ICR mice.
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http://dx.doi.org/10.1016/j.bmc.2013.07.048 | DOI Listing |
Fitoterapia
December 2024
Department of Chemistry, University of Nairobi, P. O. Box 30197-00100 Nairobi, Kenya. Electronic address:
The phytochemical investigation of the leaves and the roots of Suregada procera afforded the new ent-abietane diterpenoid sureproceriolide A (1) along with the known secondary metabolites 8,14β:11,12α-diepoxy-13(15)-abietane-16,12-olid (2), jolkinolide A (3), jolkinolide E (4), ent-pimara-8(14),15-dien-19-oic acid (5), sitosterol (6), oleana-9(11):12-dien-3β-ol (7), and oleic acid (8). Their structures were elucidated by NMR spectroscopic and mass spectrometric analyses, and the structure of jolkinolide A (3) was confirmed by single-crystal X-ray diffraction analysis. Sureproceriolide A (1) showed modest activity against the Gram-positive bacterium Staphylococcus lugdunensis (MIC = 31.
View Article and Find Full Text PDFHeliyon
February 2024
Royal Botanic Gardens Kew, Richmond, TW9 3AE, Surrey, UK.
The chemical investigation of a leaf extract from a herbarium specimen of collected in Banyang Mbo Wildlife Sanctuary, Southwest Region, Cameroon, yielded five undescribed abietane diterpenoids, banyangmbolides A-E, (-), and four known diterpenoids, gelomulides A (), B (), D () and O (). The structures of the isolated compounds were determined using NMR, IR, ECD and HRESIMS. Compounds , and , showed 48-55% inhibition at 200 μM against FM-55-M1 human melanoma cells.
View Article and Find Full Text PDFPharm Biol
December 2022
Department of Biological Sciences, Dar es Salaam University College of Education, University of Dar es Salaam, Dar es Salaam, Tanzania.
Context: Snake envenomation is one of the neglected health problems in Tanzania. Since most people, especially in rural areas, suffer from its burden, their cases are not documented due to reliance on medicinal plants. Despite the pivotal role of medicinal plants in treating snakebites, there is a paucity of information.
View Article and Find Full Text PDFJ Nat Prod
September 2022
Department of Chemistry - BMC, Uppsala University, SE-751 23 Uppsala, Sweden.
The leaf extract of gave two new modified -abietane diterpenoids, zanzibariolides A () and B (), and two known triterpenoids, simiarenol () and β-amyrin (). The structures of the isolated compounds were elucidated based on NMR and MS data analysis. Single-crystal X-ray diffraction was used to establish the absolute configurations of compounds and .
View Article and Find Full Text PDFCarbohydr Res
January 2014
State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, People's Republic of China. Electronic address:
Phytochemical investigation of the H2O extract of leaves of Suregada glomerulata led to the isolation of ten pyrrolidine-type iminosugars. The chemical structures of the six new compounds (4-6, 8-10) were elucidated as 2,5-imino-2,4,5-trideoxy-d-manno-heptitol (4-deoxy-homoDMDP) (4), 2,5-imino-2,4,5-trideoxy-d-gulo-heptitol (5), 2,5-imino-2,4,5,6-tetradeoxy-d-gulo-heptitol (6), 6-C-butyl-4-deoxy-DMDP (8), 6-C-(8-hydroxyoctyl)-DMDP (9), and 6-C-(8-hydroxyoctyl)-2,5-dideoxy-2,5-imino-d-galactitol (10), respectively, on the basis of spectroscopic data analysis (NMR and HRESIMS). Compounds 4-6 and 8 were characterized as rarely seen 4-deoxy pyrrolidine-type iminosugars.
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