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iriflophenone/aquilaria sinensis

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ČlankiKliničnih preskušanjPatenti
5 rezultatov

Effects of iriflophenone 3-C-β-glucoside on fasting blood glucose level and glucose uptake.

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Prijava / prijava
BACKGROUND One of the biological activities of agar wood (Aquilaria sinensis Lour., Thymelaeaceae), is anti-hyperglycemic activity. The methanolic extract (ME) was proven to possess the fasting blood glucose activity in rat and glucose uptake transportation by rat adipocytes. OBJECTIVE To determine

[Further chemical investigation of leaves of Aquilaria Sinensis].

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Prijava / prijava
To comprehensively utilize the rich resource of Aquilaria sinensis,the ethanol extract of the leaves of A. sinensis was further chemically investigated, which led to the isolation of 12 compounds. By means of 'H- , "C-NMR, and ESI-MS data, and through comparison with those reported in

[Simultaneous determination of benzophenones and xanthone in leaves of Aquilaria sinensis by RP-HPLC-UV].

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Prijava / prijava
This study is to develop a sensitive method by using reversed-phase high performance liquid chromatography coupled with UV detector (HPLC-UV) to simultaneously determine four bioactive compounds, iriflophenone 3-C-beta-D-glucoside, iriflophenone 3,5-C-beta-D-diglucoside, mangiferin, and

Bio-assay guided isolation and identification of α-glucosidase inhibitors from the leaves of Aquilaria sinensis.

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Prijava / prijava
Eight α-glucosidase inhibitors including four new compounds were isolated from the 70% aqueous ethanolic extract of leaves of Aquilaria sinensis (Lour.) Gilg by activity-directed fractionation and purification processes. The ethanolic extract was first separated into petroleum ether, ethyl acetate,

Synthesis and evaluation of benzophenone O-glycosides as α-glucosidase inhibitors.

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Prijava / prijava
The first total synthesis of benzophenone O-glycosides (iriflophenone 2-O-α-L-rhamnopyranoside: 1 and aquilarisinin: 2) isolated from the leaves of Aquilaria sinensis and related new derivatives (3-12) was accomplished through suitable protecting group manipulations and glycosylation starting from
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