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- W2317778314 abstract "Three new A-type proanthocyanidins (1–3), ent-epiafzelechin-(2α→O→7,4α→8)-ent-afzelechin 3′-O-β-d-glycopyranoside (1), ent-epiafzelechin-(2α→O→7,4α→8)-ent-epiafzelechin-(2α→O→7,4α→8)-ent-afzelechin (2), and ent-epiafzelechin-(2α→O→7,4α→8)-ent-epicatechin-(2α→O→7,4α→8)-ent-afzelechin (3), and three known compounds (4–6) were isolated from the whole plant of Spenceria ramalana. The structures of the new proanthocyanidins were established by spectroscopic and chemical studies. The inhibitory effects of compounds 1–6 on the formation of advanced glycation end products were examined in vitro. Compounds 3 and 6 showed the strongest inhibition, with IC50 values of 17.4 ± 0.5 and 14.1 ± 1.6 μM, respectively. The effects of these isolates on the dilation of hyaloid-retinal vessels induced by high glucose (HG) in larval zebrafish were also investigated. Compound 3 reduced the dilation of HG-induced hyaloid-retinal vessels most effectively. This compound reduced the diameters of HG-induced hyaloid-retinal vessels by about 157.7% and 164.1% at 10 and 20 μM, respectively, versus the HG-treated control group." @default.
- W2317778314 created "2016-06-24" @default.
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- W2317778314 date "2013-10-16" @default.
- W2317778314 modified "2023-10-17" @default.
- W2317778314 title "Proanthocyanidins from <i>Spenceria ramalana</i> and Their Effects on AGE Formation in Vitro and Hyaloid-Retinal Vessel Dilation in Larval Zebrafish in Vivo" @default.
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- W2317778314 doi "https://doi.org/10.1021/np400442b" @default.
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