Literature DB >> 23361306

New inhibitors of α-glucosidase in Salacia hainanensis Chun et How.

Zheng-hong Guo1, Jian Huang, Guo-sheng Wan, Xiao-ling Huo, Hui-yuan Gao.   

Abstract

The methanol extract from roots of Salacia hainanensis Chun et How afforded three new compounds, 24,26-dihydroxy-25-methoxy-tirucall-9-en-3-one (1), 2β,3β,22α-trihydroxy-lup-20(29)-ene (2) and 3β-hydroxy-2-carbonyl-lupan-29-oic acid (3), along with six known triterpenoids (4-9). Their structures were established on the basis of spectral analysis, in particular according to the data obtained by two-dimensional-NMR and high-resolution mass spectra experiments. Some of them showed much stronger inhibitory activity towards α-glucosidase than the positive control (acarbose, IC₅₀ 10.2 μM).

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Year:  2013        PMID: 23361306     DOI: 10.1007/s11418-013-0744-5

Source DB:  PubMed          Journal:  J Nat Med        ISSN: 1340-3443            Impact factor:   2.343


  7 in total

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Journal:  J Agric Food Chem       Date:  2001-04       Impact factor: 5.279

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Authors:  Hai-Ying Ma; Hui-Yuan Gao; Lu Sun; Jian Huang; Xiao-Min Xu; Li-Jun Wu
Journal:  J Nat Med       Date:  2010-09-11       Impact factor: 2.343

6.  Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis.

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Journal:  J Nat Prod       Date:  2003-09       Impact factor: 4.050

7.  Evaluation of isofagomine and its derivatives as potent glycosidase inhibitors.

Authors:  W Dong; T Jespersen; M Bols; T Skrydstrup; M R Sierks
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  7 in total

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