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New antiglycation and enzyme inhibitors from Parmotrema cooperi 被引量:2
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作者 M.Iqbal CHOUDHARY Meher ALI +4 位作者 Atia-tul-WAHAB Ajmal KHAN Saima RASHEED Sajan Lal SHYAULA(Shrestha) Atta-ur-RAHMAN 《Science China Chemistry》 SCIE EI CAS 2011年第12期1926-1931,共6页
Lichens are unique individuals which have been widely used in traditional medicines. This study was focused on the bioassayguided phytochemical investigation, and bioactivity evaluation on a lichens species, Parmotrem... Lichens are unique individuals which have been widely used in traditional medicines. This study was focused on the bioassayguided phytochemical investigation, and bioactivity evaluation on a lichens species, Parmotrema cooperi. This first bioassaydirected chemical study on P. cooperi has led to the isolation of ethyl heamatomate (1), atraric acid (2), ethyl orsellinate (3), orsellinic acid (4), lecanoric acid (5), gyrophoric acid (6), and licanorin (7). The structures of 1-7 were mainly elucidated from spectroscopic methods including 1D, and 2D NMR spectroscopy, and mass spectrometry. These compounds were evaluated for their antiglycation, urease, a-chymotrypsin, and β-glucoronidase inhibitory activities. Few of the phenolic compounds showed significant, while most of them showed good inhibition of protein glycation, and urease activities. 展开更多
关键词 LICHEN Parmotrema cooped ethyl heamatomate atraric acid urease inhibition antiglycation
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