Two new 10-hydroxy-9(10H)-anthracenone, madagascenone A (1) and B (2), were isolated from the barks of Harungana madagascariensis Lam. The structures of the compounds were determined using 1D- and 2D-NMR and mass spectroscopic techniques. Both of the compounds showed an in vitro α-glucosidase inhibition with IC = 69.9 ± 4.21 and 122.3 ± 1.13 μM, respectively, more potent than the standard acarbose (IC = 840 ± 1.23 μM).
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http://dx.doi.org/10.1080/14786419.2015.1115998 | DOI Listing |
Nat Prod Res
November 2016
d Department of Chemistry , University of Ibadan, Ibadan , Nigeria.
Two new 10-hydroxy-9(10H)-anthracenone, madagascenone A (1) and B (2), were isolated from the barks of Harungana madagascariensis Lam. The structures of the compounds were determined using 1D- and 2D-NMR and mass spectroscopic techniques. Both of the compounds showed an in vitro α-glucosidase inhibition with IC = 69.
View Article and Find Full Text PDFJ Ethnopharmacol
February 2014
Wangari Maathai Institute for Peace and Environmental Studies, P.O. Box 30197, Nairobi 00100, Kenya. Electronic address:
Ethnopharmacological Relevance: Traditional medicine plays a critical role in treatment of chronic debilitating and life threatening conditions and diseases. Cancer is one such condition whose therapeutic intervention is commonly through inexpensive traditional herbal remedies. Increasingly industrialised societies are developing drugs and chemotherapeutics from these traditional herbal plants.
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