从裂冠牛奶菜(Marsdenia incisa P. T. Li et Y. H. Li)的粗甙酸水解产物中分离得到2个已知的C_(21)甾体甙元——肉珊瑚甙元(sarcostin, Ⅰ),青羊参甙元(qingyangshengenin,Ⅱ),和一个新的C_(21)甾体甙元,命名为裂冠牛奶菜甙元A(incisag...从裂冠牛奶菜(Marsdenia incisa P. T. Li et Y. H. Li)的粗甙酸水解产物中分离得到2个已知的C_(21)甾体甙元——肉珊瑚甙元(sarcostin, Ⅰ),青羊参甙元(qingyangshengenin,Ⅱ),和一个新的C_(21)甾体甙元,命名为裂冠牛奶菜甙元A(incisagenin-A,Ⅱ)经光谱分析和化学反应,证明(Ⅲ)的结构为12-β-氧-顺芷酰去酰基萝藦甙元。展开更多
Besides a series of normal C_(21) steroids from Marsdenia incisa incisa P.T.Li et Y.P.Li, it small amount of novel C_(21) steroidal glycoside (Ⅱ) had been isolated. The mild acidic hydrolysis of (Ⅱ) afforded genin-(...Besides a series of normal C_(21) steroids from Marsdenia incisa incisa P.T.Li et Y.P.Li, it small amount of novel C_(21) steroidal glycoside (Ⅱ) had been isolated. The mild acidic hydrolysis of (Ⅱ) afforded genin-(Ⅰ). By spectroscopic analyses of IR, ELMS, FDMS, ~1H NMR, ^(13)C NMR (DEPT, PRFT), ~1H-~1H COSY, ~1H-^(13)C COSY for (Ⅰ) and (Ⅱ), (Ⅰ) had been deduced as B-nor (7) -6β-formyl-pregnane-3β, 5β, 8β, 12β, 14β, 17β, 20-heptatol, named neomarinogenin; (Ⅱ) had been deduced as neomarinogenin 3-O-β-D-thevetopyranosyl-(1→-4)-β-Dcymaropyranosyl-(1→4)-β-D-cymaropyranoside, named neomarinoside. Their physical and spectral data were as follows. Neomarinogenin (Ⅰ). A colorless prism from Me_2 CO, mp 202—205℃, 〔α〕_D^(17)+28.81°(MeOH, c0.05), C_(21)H_(34)O_8 (Found: C, 60.76; H, 8.19, C_(21)H_(34)O_8, requires C, 60.87. H, 8.21％); IRv_(max)^(KBr)cm^(-1): 3450 (OH), 1700 (C=O), 1050(C-O-C); EIMS m/z: 397 (M-OH), 380 (397-OH), 379, 378 (M-2H_2O), 36; (M-3H_2O), 342 (M-4H_2O), 333,展开更多
文摘从裂冠牛奶菜(Marsdenia incisa P. T. Li et Y. H. Li)的粗甙酸水解产物中分离得到2个已知的C_(21)甾体甙元——肉珊瑚甙元(sarcostin, Ⅰ),青羊参甙元(qingyangshengenin,Ⅱ),和一个新的C_(21)甾体甙元,命名为裂冠牛奶菜甙元A(incisagenin-A,Ⅱ)经光谱分析和化学反应,证明(Ⅲ)的结构为12-β-氧-顺芷酰去酰基萝藦甙元。
基金This work was supported by grants from International Foundation for Science in Sweden and National Science Foundation of China.
文摘Besides a series of normal C_(21) steroids from Marsdenia incisa incisa P.T.Li et Y.P.Li, it small amount of novel C_(21) steroidal glycoside (Ⅱ) had been isolated. The mild acidic hydrolysis of (Ⅱ) afforded genin-(Ⅰ). By spectroscopic analyses of IR, ELMS, FDMS, ~1H NMR, ^(13)C NMR (DEPT, PRFT), ~1H-~1H COSY, ~1H-^(13)C COSY for (Ⅰ) and (Ⅱ), (Ⅰ) had been deduced as B-nor (7) -6β-formyl-pregnane-3β, 5β, 8β, 12β, 14β, 17β, 20-heptatol, named neomarinogenin; (Ⅱ) had been deduced as neomarinogenin 3-O-β-D-thevetopyranosyl-(1→-4)-β-Dcymaropyranosyl-(1→4)-β-D-cymaropyranoside, named neomarinoside. Their physical and spectral data were as follows. Neomarinogenin (Ⅰ). A colorless prism from Me_2 CO, mp 202—205℃, 〔α〕_D^(17)+28.81°(MeOH, c0.05), C_(21)H_(34)O_8 (Found: C, 60.76; H, 8.19, C_(21)H_(34)O_8, requires C, 60.87. H, 8.21％); IRv_(max)^(KBr)cm^(-1): 3450 (OH), 1700 (C=O), 1050(C-O-C); EIMS m/z: 397 (M-OH), 380 (397-OH), 379, 378 (M-2H_2O), 36; (M-3H_2O), 342 (M-4H_2O), 333,
