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geraniin/euphorbia

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Polyphenols from Euphorbia pekinensis Inhibit AGEs Formation In Vitro and Vessel Dilation in Larval Zebrafish In Vivo.

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To identify active compounds in the roots of Euphorbia pekinensis for treatment of diabetic complications, an active column fraction from a 70% EtOH extract of E. pekinensis root was purified by preparative reversed-phase high-performance liquid chromatography, leading to the isolation of a new

Structure and biogenesis of jolkinin, a highly oxygenated ellagitannin from Euphorbia jolkinii.

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A new ellagitannin, jolkinin (2), was isolated from the fresh whole plant of Euphorbia jolkinii, and its structure, including absolute configuration, was determined on the basis of spectroscopic and chemical evidence. A highly oxygenated acyl group with unique hexacyclic structure is attached to the

Inhibitory activity for chitin synthase II from Saccharomyces cerevisiae by tannins and related compounds.

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In the course of search for potent inhibitors of chitin synthase II from natural resources, seven tannins and related compounds were isolated from the aerial part of Euphorbia pekinensis and identified as gallic acid (1), methyl gallate (2), 3-O-galloyl-(-)-shikimic acid (3), corilagin (4), geraniin

[Constituents of tannins from Euphorbia prostrata Ait].

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Ten compounds have been isolated from Euphorbia prostrata and identified as gallic acid, corilagin, 1,2,3-tri-O-galloyl-D-glucose,geraniin,tellimagradin I, II, rugosin A, rugosin E, rugosin D and rugosin G on the basis of physicochemical and spectroscopic methods.
Three new hydrolyzable tannins, euphormisins M1, M2, and M3, were isolated from Euphorbia humifusa WILLD., and respectively characterized as 1,3,6-tri-O-galloyl-4-O- brevifolincarboxyl-beta-D-glucose (19), an oxidative metabolite (23) of geraniin, and 1,3,6-tri-O-galloyl-alpha-D-glucose (18), by
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