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      厚蜂窩菌的化學(xué)成分研究

      2012-01-25 18:12:58杜子偉劉勁松吳培云何其偉
      中成藥 2012年7期
      關(guān)鍵詞:麥角柱層析波譜

      杜子偉, 劉勁松, 吳培云, 何其偉, 項 晨, 王 剛

      (安徽中醫(yī)學(xué)院藥學(xué)院現(xiàn)代中藥安徽省重點實驗室,安徽合肥230031)

      厚蜂窩菌Hexagonia speciosa為多孔菌科Polyporaceae蜂窩菌屬Hexagonia高等真菌,菌蓋扇形至貝殼型,淡黃褐色,菌肉淡黃色,薄,無味道,生于闊葉樹的腐木上,主要分布于廣東、云南等地[1]。蔣孟圓曾從該種真菌發(fā)酵液中共分離得到28個不同化合物,其中21個為新化合物。這些新化合物都是高度氧化的環(huán)乙烷類化合物,其中化合物speciosin B顯示有顯著的細(xì)胞毒活性[2-3]。為了進(jìn)一步研究厚蜂窩菌的化學(xué)成分,本實驗通過改變厚蜂窩菌的發(fā)酵條件,對其發(fā)酵液進(jìn)行了系統(tǒng)的化學(xué)成分研究,從其乙酸乙酯提取物中分離得到11個已知化合物,經(jīng)波譜解析分別鑒定為:角鯊烯 (1)、9(Z)-十八烷烯酸 (2)、麥角甾-4,6,8(14),22-四烯-3-酮 (3)、麥角甾-5,7,22-三烯-3β-醇 (4)、過氧麥角甾醇 (5)、麥角甾-6β-甲氧基-7,22-二烯-3β,5α-二醇 (6)、麥角甾-7,22-二烯-3β,5α,6β-三醇 (7)、8,14-環(huán)氧麥角甾-4,22-二烯-3,6-二酮 (8)、麥角甾-3β,5α,9α-三羥基-7,22-二烯-6-酮 (9)、2,2-二甲基-1-苯并吡喃-6-醇 (10)、2-呋喃甲酸 (11)。

      1 儀器與材料

      四川大學(xué)科學(xué)儀器廠生產(chǎn)的XRC—1型顯微熔點儀,溫度計未校正;VG AutoSpec—3000質(zhì)譜儀;Bruker AV—400和DRX—500核磁共振儀,內(nèi)標(biāo)為TMS,其中1H NMR在400 MHz和500 MHz下測定,13C NMR在100 MHz和125 MHz下測定;分析型和制備型HPLC為Agilent 1100 HPLC,色譜柱為Agilent Zorbax SB-C18和YMC柱;柱層析硅膠(80~100目和200~300目)以及GF254薄層硅膠板均為青島海洋化工廠生產(chǎn);

      反相材料 Lichroprep Rp-18(40~63 μm)為Merk公司產(chǎn)品;Sephadex LH-20為瑞典Amersham Biosciences公司產(chǎn)品;顯色方法為熒光燈下波長254nm和365nm處觀察熒光,10%硫酸乙醇溶液和硫酸香草醛處理后加熱顯色及碘蒸氣顯色。

      厚蜂窩菌Hexagonia speciosa于2007年7月份采集于云南高黎貢山,由昆明植物所楊祝良研究員鑒定,標(biāo)本存于昆明植物研究所標(biāo)本館。

      2 培養(yǎng)與發(fā)酵

      由昆明植物研究所李正輝博士培養(yǎng)發(fā)酵。培養(yǎng)基:葡萄糖5%,豬肉蛋白胨0.15%,酵母粉0.5%,KH2PO4和 MgSO4各0.05%。發(fā)酵條件:溫度24℃,初始pH 6.0,轉(zhuǎn)速250 r/min,每分鐘通氣量與罐體實際料液體積的比值為1.0,接種體積10%(V/V),種子罐發(fā)酵6 d,當(dāng)菌絲生物量最大時轉(zhuǎn)入100 L發(fā)酵罐發(fā)酵培養(yǎng)20 d。發(fā)酵液總量為63 L。

      3 提取與分離

      厚蜂窩菌發(fā)酵液 (63 L)用乙酸乙酯萃取3次,合并減壓蒸干得25 g粗提物,經(jīng)硅膠柱層析,以三氯甲烷-甲醇 (100∶0→0∶100)梯度洗脫得6個部分 (A、B、C、D、E、F)。A經(jīng)石油醚-乙酸乙酯 (100∶2→0∶100)梯度洗脫,再經(jīng)硅膠柱層析,以石油醚-乙酸乙酯 (10∶1)洗脫得到化合物1(4.5 mg)。B經(jīng)石油醚-乙酸乙酯 (100∶5→0∶100)梯度洗脫得5個亞組分,其中B1經(jīng)Sephadex LH-20柱層析,以三氯甲烷-甲醇 (1∶1)洗脫,再經(jīng)硅膠柱層析,以石油醚-乙酸乙酯 (30∶1)洗脫得到化合物2(411 mg);B2經(jīng)Sephadex LH-20柱層析,以三氯甲烷-甲醇 (1∶1)洗脫得化合物3(308 mg);B3經(jīng)反相RP-18,用甲醇-水 (90∶10→0∶100)梯度洗脫得化合物4(235 mg)和化合物5(300 mg);B5經(jīng)過硅膠柱層析,以三氯甲烷-丙酮(50∶1)洗脫得到化合物6(17 mg)和化合物7(10 mg)。C經(jīng)Sephadex LH-20柱層析,以三氯甲烷-甲醇 (1∶1)洗脫得3個亞組分,其中C1經(jīng)反相RP-18,用甲醇-水 (70∶30→0∶100)梯度洗脫,再經(jīng)硅膠柱層析,以石油醚-乙酸乙酯 (5∶1)洗脫得到化合物8(6 mg)和化合物9(7 mg);C2經(jīng)硅膠柱層析,三氯甲烷-丙酮 (30∶1)洗脫得到化合物9(4.5 mg);E經(jīng)過硅膠柱層析,用石油醚-丙酮 (100∶10→0∶100)梯度洗脫,再經(jīng)石油醚-乙酸乙酯 (2∶1)洗脫得化合物11(44 mg)。

      4 化學(xué)結(jié)構(gòu)及鑒定

      化合物1:C30H50,無色透明油狀液體。FABMS m/z:411.3 [M+H]+。1H-NMR(CDCl3,400 MHz)δ:5.08~5.15(6H,m,H-3,H-7,H-11,H-14,H-18 and H-22),1.96~2.11(20H,m,H-4,H-5,H-8,H-9,H-12,H-13,H-16,H-17,H-20 and H-21),1.68(6H,s,H-1 and H-24),1.60(18H,s,2-CH3,6-CH3,10-CH3,15-CH3,19-CH3and 23-CH3)。13C-NMR(CDCl3,100 MHz) δ:135.0(s,C-6 and C-19),134.8(s,C-10 and C-15),131.1(s,C-2 and C-23),124.4(d,C-3 and C-22),124.3(d,C-7,C-11,C-14 and C-18),39.7(t,C-5,C-9,C-16 and C-20),28.3(t,C-12 and C-13),26.8(t,C-4,C-8,C-17 and C-21),25.6(q,C-1 and C-24),17.6(q,2-CH3and 23-CH3),16.0(q,6-CH3,10-CH3,15-CH3and 19-CH3)。以上波譜數(shù)據(jù)與文獻(xiàn)[4]數(shù)據(jù)報道一致,確定該化合物為角鯊烯。

      化合物2:C18H34O2,白色油狀物。EI-MS m/z(%):282 [M]+(27),264(50),256(36),111(47),97(70),83(74),69(80),57(70),55(100)。1H-NMR(CDCl3,400 MHz)δ:5.34(2H,m,H-9 and H-10),2.34(2H,t,J=7.5 Hz,H-2),2.04(4H,m,H-8 and H-11),1.61(2H,m,H-3),1.20~1.35(m,H-4~H-7 and H-12~H-17),0.89(3H,t,J=6.8 Hz,H-18)。13C-NMR(CDCl3,100 MHz)δ:180.6(s,C-1),130.0(d,C-10),129.7(d,C-9),34.1(t,C-2),31.9(t,C-16),29.0~29.7(t,C-4~C-7 and C-12~C-15),27.2(t,C-8 and C-11),24.6(t,C-3),22.7(t,C-17),14.1(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[5]數(shù)據(jù)報道一致,確定該化合物為9(Z)-十八烷烯酸。

      化合物3:C28H40O,淺黃色晶體。mp 112~114℃。EI-MS m/z(%):392[M]+(15),377(3),349(4),268(100),253(30),214(26),173(23),69(47)。1H-NMR(CDCl3,400 MHz)δ:6.58(1H,d,J=9.4 Hz,H-7),6.00(1H,d,J=9.4 Hz,H-6),5.70(1H,s,H-4),5.24(1H,dd,J=15.2,7.2 Hz,H-23),5.18(1H,dd,J=15.2,7.2 Hz,H-22),1.21~2.53(18H,m,甾體母核),1.03(3H,d,J=6.8 Hz,H-21),0.97(3H,s,H-19),0.93(3H,s,H-18),0.90(3H,d,J=6.8 Hz,H-28),0.82(3H,d,J=6.8 Hz,H-27),0.78(3H,d,J=6.8 Hz,H-26)。13C-NMR(CDCl3,100 MHz)δ:199.3(s,C-3),164.2(s,C-5),156.0(s,C-14),135.0(d,C-22),133.9(d,C-7),132.6(d,C-23),124.5(d,C-6),124.3(s,C-8),123.0(d,C-4),55.8(d,C-17),44.0(d,C-9),44.0(s,C-13),42.9(d,C-24),39.2(d,C-20),36.8(s,C-10),35.7(t,C-15),34.2(t,C-12),34.1(t,C-1),33.1(d,C-25),27.7(t,C-16),25.4(t,C-11),21.2(q,C-21),20.0(q,C-27),19.7(q,C-26),19.0(t,C-2),18.9(q,C-19),17.6(q,C-28),16.7(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[6]數(shù)據(jù)報道一致,確定該化合物為麥角甾-4,6,8(14),22-四烯-3-酮。

      化合物4:C28H44O,白色晶體。mp 152~154℃。EI-MS m/z(%):396[M]+(55),363(61),337(40),271(17),253(48),211(37),197(28),185(23),171(30),157(55),143(57),131(27),119(30),91(28),81(27),69(100),55(56)。1H-NMR(CDCl3,400 MHz)δ:5.58(1H,m,H-6),5.38(1H,m,H-7),5.14~5.26(2H,m,H-22 and H-23),3.60(1H,m,H-3),1.03(3H,d,J=6.8 Hz,H-21),0.95(3H,s,H-19),0.92(3H,d,J=6.8 Hz,H-28),0.84(3H,d,J=6.8 Hz,H-27),0.82(3H,d,J=6.8 Hz,H-26), 0.61(3H, s, H-18)。13C-NMR(CDCl3,100 MHz)δ:141.3(s,C-8),139.8(s,C-5),135.6(d,C-22),132.1(d,C-23),119.6(d,C-6),116.4(d,C-7),70.5(d,C-3),55.9(d,C-17),54.6(d,C-14),46.4(d,C-9),42.9(s,C-13),40.8(d,C-24),40.9(t,C-4),40.4(d,C-20),39.2(t,C-12),38.4(t,C-1),37.1(s,C-10),33.1(d,C-25),32.1(t,C-2),28.3(t,C-16),23.0(t,C-15),21.2(t,C-11),21.2(q,C-21),19.9(q,C-26),19.7(q,C-27),17.6(q,C-28),16.3(q,C-19),12.1(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[7]數(shù)據(jù)報道一致,確定該化合物為麥角甾-5,7,22-三烯-3β-醇。

      化合物5:C28H44O3,無色針晶。mp 177~178℃。EI-MS m/z(%):428[M]+(10),410(4),396(100),363(35),271(7),255(37),251(14),152(30),107(22),69(63)。1H-NMR(CDCl3,400 MHz):δ:6.50(1H,d,J=8.4 Hz,H-7),6.24(1H,d,J=8.4 Hz,H-6),5.22(1H,dd,J=15.2,7.4 Hz,H-22),5.13(1H,dd,J=15.2,7.4 Hz,H-23),3.97(1H,m,H-3),0.99(3H,d,J=6.8 Hz,H-21),0.90(3H,d,J=6.8 Hz,H-28),0.88(3H,s,H-19),0.83(3H,d,J=6.8 Hz,H-27),0.82(3H,s,H-18),0.80(3H,d,J=6.8 Hz,H-26)。13C-NMR(CDCl3,100 MHz):δ:135.4(d,C-6),135.2(d,C-22),132.3(d,C-23),130.7(d,C-7),82.1(s,C-5),79.4(s,C-8),66.4(d,C-3),56.2(d,C-17),51.6(d,C-14),51.0(d,C-9),44.5(s,C-13),42.7(d,C-24),39.7(d,C-20),39.3(t,C-12),36.9(t,C-4),36.9(s,C-10),34.7(t,C-1),33.0(d,C-25),30.1(t,C-2),28.6(t,C-15),23.4(t,C-11),20.8(q,C-21),20.6(t,C-16),19.9(q,C-27),19.6(q,C-26),18.1(q,C-19),17.5(q,C-28),12.8(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[8]數(shù)據(jù)報道一致,確定該化合物為過氧麥角甾醇。

      化合物 6:C29H48O3,白色粉末。EI-MS m/z(%):444 [M]+(6),426(80),411(26),393(40),377(100),301(11),269(32),251(76)。1H-NMR(CDCl3,400 MHz)δ:5.41(1H,brd,J=5.0 Hz,H-7),5.13~5.25(2H,m,H-22 and H-23),4.05(1H,m,H-3),3.39(3H,s,6-OCH3),3.17(1H,brd,J=4.7 Hz,H-6),1.03(3H,d,J=6.5 Hz,H-21),1.00(3H,s,H-19),0.92(3H,d,J=6.5 Hz,H-28),0.84(3H,d,J=6.5 Hz,H-27),0.82(3H,d,J=6.5 Hz,H-26),0.60(3H,s,H-18)。13C-NMR(CDCl3,100 MHz)δ:143.6(s,C-8),135.5(d,C-22),132.0(d,C-23),114.9(d,C-7),82.5(d,C-6),76.4(s,C-5),67.8(d,C-3),58.4(q,6-OCH3),55.9(d,C-17),54.9(d,C-14),43.8(d,C-9),43.8(s,C-13),42.8(d,C-24),40.4(d,C-20),39.5(t,C-4),39.3(t,C-12),37.2(s,C-10),33.0(d,C-25),32.7(t,C-1),30.8(t,C-2),27.9(t,C-16),22.8(t,C-15),22.2(t,C-11),21.1(q,C-21),19.8(q,C-26),19.6(q,C-27),18.5(q,C-19),17.6(q,C-28),12.3(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[9]數(shù)據(jù)報道一致,確定該化合物為麥角甾-6β-甲氧基-7,22-二烯-3β,5α-二醇。

      化合物7:C28H46O3,白色粉末。mp 224~226℃。EI-MS m/z(%):430[M]+(35),412(35),394(37),379(65),376(15),269(33),251(62),69(100)。1H-NMR(C5D5N,400 MHz)δ:5.74(1H,brs,H-7),5.24(1H,dd,J=15.2,7.4 Hz,H-23),5.16(1H,dd,J=15.2,7.4 Hz,H-22),4.84(1H,m,H-3),4.32(1H,brd,J=4.8 Hz,H-6),1.53(3H,s,H-19),1.07(3H,d,J=6.8 Hz,H-21),0.94(3H,d,J=6.8 Hz,H-28),0.85(3H,d,J=6.8 Hz,H-27),0.84(3H,d,J=6.8 Hz,H-26),0.67(3H,s,H-18)。13CNMR(C5D5N,100 MHz)δ:141.6(s,C-8),136.2(d,C-22),132.5(d,C-23),120.4(d,C-7),76.5(s,C-5),74.3(d,C-6),67.6(d,C-3),56.5(d,C-17),55.2(d,C-14),43.9(s,C-13),43.8(d,C-9),43.0(d,C-24),42.0(t,C-4),40.7(d,C-20),40.1(t,C-12),38.1(s,C-10),33.8(t,C-1),33.1(d,C-25),32.6(t,C-2),28.2(t,C-16),23.5(t,C-15),22.4(t,C-11),21.3(q,C-21),20.1(q,C-27),19.9(q,C-26),18.8(q,C-19),17.6(q,C-28),12.3(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[10]數(shù)據(jù)報道一致,確定該化合物為麥角甾-7,22-二烯-3β,5α,6β-三醇。

      化合物 8:C28H40O3,白色粉末,EI-MS m/z(%):424[M]+(20),409(5),396(5),381(5),327(5),300(5),285(15),257(10),229(30),189(10),175(5),150(15),137(30),109(25),69(100),55(65)。1H-NMR(CDCl3,500 MHz)δ:6.35(1H,s,H-4),5.22 ~ 5.30(2H,m,H-22 and H-23),2.80(1H,t,J=8.9 Hz,H-9),2.63(1H,d,J=16.7 Hz,H-7a),2.48(1H,d,J=16.7 Hz,H-7b),2.02~2.04(2H,m,H-1),1.86~1.89(1H,m,H-24),1.25(3H,s,H-19),1.08(3H,d,J=6.8 Hz,H-21),0.98(3H,s,H-18),0.91(3H,d,J=6.8 Hz,H-28),0.83(3H,d,J=6.8 Hz,H-27),0.81(3H,d,J=6.8 Hz,H-26)。13C-NMR(CDCl3,125 MHz)δ:216.0(s,C-6),200.0(s,C-3),157.4(s,C-5),135.4(d,C-22),132.6(d,C-23),126.8(d,C-4),71.5(s,C-8),62.5(s,C-14),54.2(s,C-13),49.8(d,C-9),49.6(d,C-17),43.5(d,C-24),41.2(t,C-7),39.9(s,C-10),39.2(t,C-1),38.7(t,C-15),38.1(t,C-2),37.5(d,C-20),34.6(t,C-16),33.3(d,C-25),25.3(t,C-11),24.2(q,C-19),23.8(q,C-21),23.4(t,C-12),20.2(q,C-27),19.9(q,C-26),17.8(q,C-28),17.3(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[11]數(shù)據(jù)報道一致,確定該化合物為8,14-環(huán)氧麥角甾-4,22-二烯-3,6-二酮。

      化合物9:C28H44O4,白色粉末。EI-MS m/z(%):444[M]+(2),410(4),392(5),377(4),363(3),316(13),283(6),267(17),251(15),215(11),187(16),173(15),161(18),143(22),125(19),109(25),95(28),81(42),69(100),55(80)。1H-NMR(C5D5N,400 MHz)δ:5.93(1H,brs,H-7),5.26(1H,dd,J=15.2,7.9 Hz,H-23),5.19(1H,dd,J=15.2,7.9 Hz,H-22),4.62(1H,m,H-3),1.15(3H,s,H-19),1.05(3H,d,J=6.8 Hz,H-21),0.96(3H,d,J=6.8 Hz,H-28),0.86(3H,d,J=6.8 Hz,H-27),0.85(3H,d,J=6.8 Hz,H-26),0.64(3H,s,H-18)。13C-NMR(C5D5N,100 MHz)δ:199.1(s,C-6),164.1(s,C-8),136.2(d,C-22),132.5(d,C-23),120.3(d,C-7),79.8(s,C-5),75.1(s,C-9),66.8(d,C-3),56.2(d,C-17),52.0(d,C-14),45.4(s,C-13),43.1(d,C-24),42.3(s,C-10),40.6(d,C-20),38.1(t,C-4),35.5(t,C-12),33.4(d,C-25),31.5(t,C-2),29.0(t,C-11),28.4(t,C-16),26.4(t,C-1),22.8(t,C-15),21.3(q,C-21),20.4(q,C-19),20.2(q,C-27),19.9(q,C-26),17.9(q,C-28),12.4(q,C-18)。以上波譜數(shù)據(jù)與文獻(xiàn)[12]數(shù)據(jù)報道一致,確定該化合物為麥角甾-3β,5α,9α-三羥基-7,22-二烯-6-酮。

      化合物10:C11H12O2,棕黃色無定形粉末,mp 86~87℃。ESI-MS m/z:353[2M+H],177[M+H]。1H-NMR(CDCl3,400 MHz)δ:6.65(1H,d,J=8.6 Hz,H-8),6.58(1H,dd,J=8.6,2.9 Hz,H-7),6.49(1H,d,J=2.9 Hz,H-5),6.25(1H,d,J=9.8 Hz,H-4),5.64(1H,d,J=9.8 Hz,H-3),1.41(6H, s, 2-2CH3)。13C-NMR(CDCl3,100 MHz)δ:149.4(s,C-6),146.7(s,C-9),131.9(d,C-3),122.1(d,C-4),122.0(s,C-10),116.9(d,C-8),115.4(d,C-7),112.8(d,C-5),75.8(s,C-2),27.5(q,2-2CH3)。以上波譜數(shù)據(jù)與文獻(xiàn)[13]數(shù)據(jù)報道一致,確定該化合物為2,2-二甲基-1-苯并吡喃-6-醇。

      化合物 11:C5H4O3,白色晶體,mp 210~211℃。EI-MS m/z(%):112[M]+(100),95(75),55(6),39(47),38(14),37(8),29(8)。1H-NMR(CDCl3,400 MHz)δ:7.66(1H,d,J=1.7 Hz,H-5),7.35(1H,d,J=3.4 Hz,H-3),6.58(1H,dd,J=3.4,1.6 Hz,H-4)。13C-NMR(CDCl3,100 MHz)δ:163.4(s,2-COOH),147.4(d,C-5),143.8(s,C-2),120.0(d,C-3),112.2(d,C-4)。以上波譜數(shù)據(jù)與文獻(xiàn)[14]數(shù)據(jù)報道一致,確定該化合物為2-呋喃甲酸。

      [1]趙繼鼎.中國真菌志:第3卷[M].北京:科學(xué)出版社,1998:186.

      [2]Jiang M Y,Zhang L,Liu R.Speciosins A-K,oxygenated cyclohexanoids from the basidiomycete Hexagonia speciosa[J].J Nat Prod,2009,72:1405.

      [3]Jiang M Y,Li Y,Wang F.Isoprenylated cyclohexanoids from the basidiomycete Hexagonia speciosa[J].Phytochemistry,2011,72(9):923-928.

      [4]Burger B V,Roux M L,Spies S C,et al.Mammalian pheromone studies-III.(e,e)-7,11,15-trimethyl-3-methylenehexa-deca-1,6,10,14-tetraene,a new diterpene analogue of β-farnesene from the dorsal gland of the springbok,Antidorcas marsupialis[J].Tetrahedron Letters,1978,19(52):5221.

      [5]Akita C,Kawaguchi T,Kaneko F,et al.Solid-state13C NMR study on order→disorder phase transition in oleic acid[J].J Phys Chem B,2004,108(15):4862.

      [6]Gao J M,Dong Z J,Liu J K.A new ceramide from the basidiomycete Russula cyanoxantha[J].Lipids,2001,36(2):175.

      [7]Mishra P D,Wahidulla S,Souza L D.Lipid constituents of marine sponge Suberitus carnosus[J].Ind J Chem,1996,35B:806.

      [8]Ishizuka T,Yaoita Y,Kikuchi M.Sterols from the fruit bodies of Grifola frondosa[J].Chem Pharm Bull,1997,45:1756.

      [9]Du Z Z,Shen Y M.A rare new cleistanthane diterpene from the pericarp of Trewia nudiflora[J].Helvetica Chimica Acta,2006,89:2841.

      [10]Gao J M,Hu L,Liu J K.A novel sterol from Chinese truffles Tuber indicum[J].Steroids,2001,66:771.

      [11]Gallo M B,Cavalcanti B C,Barros F W,et al.Chemical constituents of Papulaspora immersa,an endophyte from Smallanthus sonchifolius(Asteraceae),and their cytotoxic activity[J].Chem Biodivers,2010,7:2941.

      [12]Yaoita Y,Amemiya K,Ohnuma H,et al.Sterol constituents from five edible mushrooms[J].Chem Pharm Bull,1998,46:944.

      [13]Brown P E,Lewis R A,Waring M A.Studies of chromenes.Part 9.Syntheses of chromenequinones[J].J Chem Soc Perkin Trans 1,1990,11:2979.

      [14]張維威,孔令義.栽培毛喉鞘蕊花化學(xué)成分[J].中國中藥雜志,2009,34(16):2060.

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