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Ocotillol-type derivatives (II) synthesis and protective effects on cultured anoxia/reoxygen injury myocardiocytes

机译:Ocotillol型衍生物(II)的合成及其对培养的缺氧/复氧损伤心肌细胞的保护作用

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The ocotillol-type derivatives (3β, 12β)-12, 25-dihydroxy-20S, 24R-epoxy-dammar-24-en-3-yl-2-O-β-D-glucopyranosyl-β-D-glucopyranoside and (3β, 6α, 12β)-3, 12, 25- trihydroxy- 20S, 24R- epoxy- dammar-24-en-6-yl-2-O-[6-deoxy-α-L-mannopyranosyl]-β-D-glucopyranoside (3a and b) had been designed and synthesized from 20 (S)-Rg3 and 20 (S)-Rg2 which structures were confirmed byelectrospray ionization mass spectrometry(ESI-MS),Hydrogen-Nuclear magnetic resonance(1H-NMR)andcarbon-Nuclear magnetic resonance(13C-NMR). 20(S)-Rg3, 20(S)-Rg2, 3a and b were evaluatedIn vitrofor its protective effect on cultured myocardiocytes with anoxia /reoxygen injury. The pharmaceutical data appeared that these four compounds had protective effect and 3a showed the most potent bioactivity among them.
机译:卵磷脂型衍生物(3β,12β)-12、25-二羟基-20S,24R-环氧-达玛-24-en-3-基-2-O-β-D-吡喃葡萄糖基-β-D -吡喃葡萄糖苷和(3β,6α,12β)-3,12,25-三羟基20S,24R-环氧-dammar-24-en-6-基-2-O- [6-脱氧-α-从20(S)-Rg3和20(S)-Rg2设计并合成了L-甘露吡喃糖基]-β-D-吡喃葡萄糖苷(3a和b),其结构通过电喷雾电离质谱(ESI-MS),氢确定-核磁共振(1H-NMR)和碳-核磁共振(13C-NMR)。体外评估了20(S)-Rg3、20(S)-Rg2、3a和b对缺氧/复氧损伤培养的心肌细胞的保护作用。药物数据表明这四种化合物具有保护作用,而3a显示出其中最强的生物活性。

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