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      夏枯草莖葉中三萜類成分研究

      2016-03-10 04:21:44蔡凡嚴(yán)啟新深圳市龍崗區(qū)婦幼保健院藥劑科廣東深圳587深圳市海王生物工程股份有限公司廣東深圳58057
      廣東藥科大學(xué)學(xué)報 2016年4期
      關(guān)鍵詞:夏枯草化學(xué)成分

      蔡凡,嚴(yán)啟新(.深圳市龍崗區(qū)婦幼保健院藥劑科,廣東深圳587;.深圳市海王生物工程股份有限公司,廣東深圳58057)

      夏枯草莖葉中三萜類成分研究

      蔡凡1,嚴(yán)啟新2
      (1.深圳市龍崗區(qū)婦幼保健院藥劑科,廣東深圳518172;2.深圳市海王生物工程股份有限公司,廣東深圳518057)

      目的研究夏枯草莖葉中的化學(xué)成分。方法 采用正反相硅膠、Sephadex LH-20凝膠、ODS柱層析等手段,對夏枯草莖葉體積分數(shù)80%乙醇提取物的乙酸乙酯部位進行分離純化,再采用紫外、紅外、質(zhì)譜法進行結(jié)構(gòu)鑒定。結(jié)果從夏枯草莖葉中分離得到7個烏蘇烷型三萜類化合物:烏蘇酸(1)、1β,3β-二羥基烏蘇烷-12烯-28-酸(2)、2α,3β-二羥基烏蘇烷-12烯-28-酸(3)、3-O-α-L-阿拉伯吡喃糖-19α-羥基-烏蘇烷-12烯-28-酸(4)、3β,23-二羥基-烏蘇烷-12烯-28-酸(5)、2α,3β,19α,23β-四羥基烏蘇烷-12烯-28-酸(6)、3α,19α,23,24-四羥基-烏蘇烷-12烯-28-酸(7)。結(jié)論化合物2、4~7為首次從該植物中分離得到。關(guān)鍵詞:夏枯草;化學(xué)成分;烏蘇烷型三萜類化合物

      夏枯草Prunella vulgaris L.為唇形科夏枯草屬植物,其果穗作為常用中藥夏枯草收載于歷版《中國藥典》,具有清火明目、散結(jié)消腫之功效,用于治療目赤腫痛、頭痛眩暈、高血壓等癥[1]。據(jù)考證,夏枯草入藥部位古代用莖葉,現(xiàn)代用果穗[2]。國內(nèi)外對夏枯草果穗的研究較多,但夏枯草莖葉的報道很少。夏枯草主要含三萜皂苷、蕓香苷、金絲桃苷等苷類物質(zhì)及熊果酸、咖啡酸、游離齊敦果酸等有機酸,花穗中含飛燕草素、矢車菊素的花色苷、d-樟腦、d-小茴香酮等[1]。為了研究夏枯草莖葉與果穗中化學(xué)成分的異同,擴大用藥范圍、合理開發(fā)利用該植物資源,本文對夏枯草莖葉的化學(xué)成分進行了研究,從80%(體積分數(shù),下同)乙醇提取物的乙酸乙酯部位分離和鑒定了7個烏蘇烷型三萜類化合物。

      1 儀器與材料

      Büchi Melting point B-540型熔點測定儀(瑞士Büchi公司),溫度未經(jīng)校較正;LCQ DECAXPplus質(zhì)譜儀(美國菲尼根質(zhì)譜公司);Bruker AM 500型核磁共振儀(德國Brucker公司,TMS為內(nèi)標(biāo));DMSO-d6(批號B00038104,上海楚柏實驗室設(shè)備有限公司)。柱層析硅膠(200~300目,青島海洋化工有限公司),薄層層析硅膠(青島海洋化工有限公司),凝膠Sephadex LH-20(Pharmacia),ODS SepaxGP-C18(40~60 μm,Sepax Technologies Inc.)。

      夏枯草莖葉于2009年5月采自安徽蕪湖,原植物經(jīng)嚴(yán)啟新博士鑒定為夏枯草Prunella vulgaris L.,標(biāo)本保管在深圳市龍崗區(qū)婦幼保健院。

      2 提取與分離

      取自然干燥夏枯草莖葉5 kg,粉碎,經(jīng)80%乙醇40 kg加熱回流提取2次,每次2 h,提取液濃縮得浸膏2.1 kg。用5 L水溶液使之混懸,再分別用乙酸乙酯3 kg、正丁醇4 kg萃取,回收溶劑,得乙酸乙酯部分200 g。取乙酸乙酯萃取部位(180 g)進行硅膠柱色譜,以三氯甲烷-甲醇(體積比100∶0,20∶1,10∶1,5∶1,1∶1,0∶100)梯度洗脫,得到Fr.1~Fr.6共6個流分(各流分質(zhì)量為15 g左右)。將以上各個流分經(jīng)反復(fù)硅膠柱層析、凝膠柱層析、反相C18柱層析進行分離,分別從Fr.1~Fr.5得到化合物1(90 mg)、2(8 mg)、3(35 mg)、4(9 mg)、5(15 mg),從Fr.6得到化合物6(55 mg)、7(9 mg)。

      3 結(jié)構(gòu)鑒定

      化合物1:白色粉末(甲醇),mp 260~261℃。ESI-MS m/z:457[M+H]+。1H-NMR(400 MHz,C5D5N)δ:5.58(1H,br.s,H-12),3.57(1H,dd,J= 5.9,5.7 Hz,H-3),2.74(1H,d,J=11.3 Hz,H-18),1.34(3H,s,H-23),1.32(3H,s,H-27),1.15(3H,s,H-26),1.10(3H,s,H-25),0.90(3H,s,H-24),1.09 (3H,d,J=8.2 Hz,H-30),1.05(3H,d,J=4.8 Hz,H-29)。13C-NMR(400 MHz,C5D5N)δ:180.0(C-28),139.4(C-13),125.8(C-12),78.2(C-3),56.0(C-5),53.7(C-18),48.2(C-9),48.2(C-17),42.6(C-14),40.1(C-8),39.6(C-19),39.5(C-20),39.4(C-4),39.2(C-1),37.6(C-22),37.4(C-10),33.7(C-7),31.2(C-21),28.9(C-23),28.8(C-15),28.2(C-2),25.0(C-16),24.0(C-11),23.8(C-27),21.5(C-30),18.9(C-6),17.6(C-26),17.5(C-29),16.7(C-24),15.8(C-25)。以上數(shù)據(jù)與文獻[3]對照基本一致,故鑒定化合物1為烏蘇酸(ursolic acid)。

      化合物2:白色粉末(甲醇),mp 122~123℃。ESI-MS m/z:473[M+H]+。1H-NMR(400 MHz, C5D5N)δ:5.58(1H,br.s,H-12),3.63(1H,dd,Jaa= 11.5 Hz,Jae=5.2 Hz,H-1),3.40(1H,dd,Jaa= 11.6 Hz,Jae=5.0 Hz,H-3),1.37(3H,s,H-23),1.32 (3H,s,H-27),1.12(3H,s,H-26),1.11(3H,s,H-25),0.95(3H,s,H-24),1.09(3H,d,J=7.2 Hz,H-30),1.03(3H,d,J=6.5 Hz,H-29)。13C-NMR(400 MHz,C5D5N)δ:180.3(C-28),140.9(C-13),124.1 (C-12),78.8(C-1),78.1(C-3),55.9(C-5),52.8(C-18),48.2(C-17),46.7(C-9),42.3(C-14),40.0(C-8),39.8(C-20),39.4(C-19),39.0(C-4),38.6(C-10),37.5(C-22),34.3(C-7),33.3(C-21),31.0(C-21),30.9(C-2),28.4(C-23),28.2(C-15),26.2(C-16),23.9(C-11),24.8(C-27),22.6(C-30),19.8(C-6),18.5(C-29,25),17.7(C-26),16.6(C-24)。以上數(shù)據(jù)與文獻[4]對照基本一致,故鑒定化合物2為1β,3β-二 羥 基 烏 蘇 烷-12烯-28-酸 (1β,3βdihydroxyurs-12-en-28-oic acid)。

      化合物3:白色粉末(甲醇),mp 253~254℃。ESI-MS m/z:473[M+H]+。1H-NMR(400 MHz,C5D5N)δ:5.56(1H,t,J=3.2 Hz,H-12),4.16(1H,m,H-2β),3.44(1H,d,J=9.4 Hz,H-3),2.70(1H,d,J=11.2 Hz,H-18),1.36(3H,s,H-23),1.28(3H,s,H-27),1.18(3H,s,H-26),1.16(3H,s,H-25),1.13 (3H,s,H-24),1.14(3H,d,J=6.4 Hz,H-30),1.12 (3H,d,J=6.4 Hz,H-29)。13C-NMR(400 MHz,C5D5N)δ:180.0(C-28),139.4(C-13),125.6(C-12),83.9(C-3),68.7(C-2),56.0(C-5),53.6(C-18),48.2(C-17,1),48.1(C-9),42.6(C-14),40.1 (C-8),40.0(C-4),39.6(C-19),39.5(C-20),38.5 (C-10),37.6(C-22),33.6(C-7),31.2(C-21),29.5 (C-23),28.7(C-15),25.0(C-16),24.0(C-11),23.8 (C-27),21.5(C-30),19.0(C-6),17.8(C-29),17.6 (C-26),17.5(C-24),17.1(C-25)。以上數(shù)據(jù)與文獻[5]對照基本一致,鑒定化合物3為2α,3β-二羥基烏蘇烷-12烯-28-酸(2α,3β-dihydroxyurs-12-en-28-oic acid)。

      化合物4:白色粉末(甲醇),mp 243~245℃。ESI-MS m/z:627[M+Na]+。1H-NMR(400 MHz,C5D5N)δ:5.64(1H,br.s,H-12),5.45(1H,t,J= 8.7 Hz,H-3),5.21~3.95(5H,glc-H),3.14(1H,s,H-18),1.82(3H,s,H-23),1.50(3H,s,H-24),1.26 (3H,s,H-27),1.16(3H,s,H-26),0.91(3H,s,H-25),1.05(3H,d,J=6.3 Hz,H-29),1.21(3H,d,J= 6.3 Hz,H-30)。13C-NMR(400 MHz,C5D5N)δ:180.9 (C-28),140.1(C-13),128.1(C-12),106.4(C-glc-1),89.0(C-3),82.2(C-glc-3),75.2(C-glc-4),73.9 (C-glc-2),72.8(C-19),63.9(C-glc-5),55.9(C-5),54.8(C-18),47.8(C-17),47.8(C-9),42.5(C-20),42.3(C-14),40.5(C-8),39.6(C-1,4),38.6(C-22),37.0(C-10),33.7(C-7),30.1(C-15),29.5(C-23),28.3(C-2),27.3(C-29),27.1(C-21),26.6(C-16),24.9(C-27),24.1(C-11),18.8(C-6),17.3(C-26),17.0(C-30),16.9(C-24),15.6(C-25)。以上數(shù)據(jù)與文獻[6]對照基本一致,鑒定化合物4為3-O-α-L-阿拉伯吡喃糖基-19α-羥基-烏蘇烷-12烯-28-酸(3-O-α-L-arabinophyranose-19α-hydroxylurs-12-en-28-oic acid)。

      化合物5:白色粉末(甲醇),mp 283~287℃。ESI-MS m/z:495[M+Na]+。1H-NMR(400 MHz,C5D5N)δ:5.32(1H,t,J=3.5 Hz,H-12),4.00(1H,d,J=10.6 Hz,H-23),3.58(1H,d,J=10.6 Hz,H-23),3.56(1H,m,H-3),1.34(3H,s,H-24),1.32 (3H,s,H-26),1.14(3H,s,H-27),1.12(3H,s,H-25),1.05(3H,d,J=2.8 Hz,H-30),1.03(3H,d,J= 6.5 Hz,H-29)。13C-NMR(400 MHz,C5D5N)δ:180.0 (C-28),139.7(C-13),125.2(C-12),78.2(C-3),69.3(C-23),55.9(C-5),54.8(C-18),48.2(C-17),47.8(C-9),40.4(C-14),40.0(C-4),39.9(C-8),39.5 (C-19),39.4(C-20),38.8(C-1),37.3(C-10),36.3(C-22),33.4(C-7),31.4(C-21),28.9(C-15),26.7(C-2),24.0(C-16),23.8(C-27),23.7(C-11),21.8(C-30),18.9(C-6),17.9(C-29),17.1(C-26),16.7(C-25),16.0 (C-24)。以上數(shù)據(jù)與文獻[7]對照基本一致,鑒定化合物5為3β,23-二羥基烏蘇烷-12烯-28-酸(3β,23-dihydroxyurs-12-en-28-oic acid)。

      化合物6:白色粉末(甲醇),mp 283~285℃。ESI-MS m/z:505[M+H]+。1H-NMR(400 MHz,CD3OD)δ:5.30(1H,m,H-12),4.35~3.45(4H,m,H-23a,23b,3,2),2.51(1H,s,H-18),1.30(3H,s,H-24),1.30(3H,s,H-26),1.18(3H,s,H-27),1.05(3H,s,H-25),1.05(3H,s,H-29),0.92(3H,d,J=6.7 Hz,H-30)。13C-NMR(400 MHz,CD3OD)δ:182.5(C-28),139.6(C-13),130.0(C-12),82.8(C-3),74.4(C-19),69.1(C-2),67.3(C-23),55.4(C-18),50.1(C-5),49.9 (C-17),48.7(C-9),44.4(C-1),43.4(C-4),43.3(20),42.0(C-14),41.8(C-8),40.5(C-10),39.3(C-22),34.0 (C-7),29.7(C-15),27.9(C-21),27.6(C-16),27.4 (C-11),25.3(C-29),25.1(C-24),24.9(C-27),18.8 (C-25),18.0(C-6),16.9(C-30),14.4(C-26)。以上數(shù)據(jù)與文獻[8]對照基本一致,鑒定化合物6為2α,3β,19α,23-四羥基烏蘇烷-12烯-28-酸(2α,3β,19α,23βtetrahydroxyurs-12-en-28-oic acid)。

      化合物7:白色粉末(甲醇),mp 283~285℃。ESI-MS m/z:505[M+H]+。1H-NMR(400 MHz,CD3OD)δ:5.26(1H,m,H-12),4.12(1H,d,J= 11.4 Hz,H-23a),4.06(1H,d,J=11.3 Hz,H-24a),3.75 (1H,dd,J=11.6,4.5 Hz,H-3),3.64(1H,d,J= 11.3 Hz,H-23b),3.55(1H,d,J=11.4 Hz,H-24b),2.49 (1H,s,H-18),1.34(3H,s,H-26),1.19(3H,s,H-27),0.97(3H,s,H-29),0.78(3H,s,H-25),0.94(3H,d,J= 6.7 Hz,H-30)。13C-NMR(400 MHz,CD3OD)δ:182.5 (C-28),140.3(C-13),129.6(C-12),73.2(C-19),70.9 (C-3),69.0(C-23),63.7(C-24),55.4(C-18),49.0(C-17),48.7(C-9),47.5(C-5),46.1(C-4),43.4(C-20),42.9(C-14),41.3(C-8),39.3(C-22),38.0(C-10),34.3(C-1,7),29.9(C-15),28.3(C-29),27.6 (C-16),27.3(C-2),26.9(C-21),25.2(C-27),25.1 (C-11),20.1(C-6),17.7(C-26),16.9(C-30),16.5 (C-25)。以上數(shù)據(jù)與文獻[9]對照基本一致,鑒定化合物7為3α,19α,23,24-四羥基-烏蘇烷-12烯-28-酸(3α,19α,23,24-tetrahydroxyurs-12-en-28-oic acid)。

      [1]國家藥典委員會.中華人民共和國藥典:2015年版一部[M].北京:中國醫(yī)藥科技出版社,2015:280.

      [2]陳宇航,郭巧生,王澄亞.夏枯草本草及其入藥部位變化的考證[J].中國中藥雜志,2010,35(2):242-246.

      [3]呂寒,陳劍,李維林,等.枇杷葉中三萜類化學(xué)成分的研究[J].中藥材,2008,31(9):1351-1354.

      [4]SALIMUZZAMAN S,F(xiàn)ARRUKH H,SABIRA B,et al. Kaneric acid,a new triterpene from the leaves of Nerium oleander[J].J Nat Prod,1986,49(6):1086-1090.

      [5]KUANG H X,KASAI R,OHTANI K,et al.Chemical constituents of pericarps of Rosa davurica Pall.,a traditional Chinese medicine[J].Chem Pharm Bull,1989,37(8): 2232-2233.

      [6]賀清輝,李會軍,畢志明,等.紅腺忍冬藤莖的化學(xué)成分[J].中國天然藥物,2006,5(4):385-386.

      [7]INADA A,YAMADA M,MURITA H,et al.Phytochemical studies of seeds of medicinal plants.I.Two sulfated triterpenoid glycosides,sulfapatrinosides I and II,from seeds of Patrinia scabiosaefolia Fischer[J].Chem Pharm Bull,1988,36(11):4269-4274.

      [8]SHIGENAGA S,KOUNO I,KAWANO N.triterpenoids and glycosides from Geum japonicum[J].Phytochemistry,1985,24(1):115-118.

      [9]ZHAO W M,WOLFENDER J L,CHENG K,et al. Triterpenes andtriterpenoidsaponinsfromMussaenda pubescens[J].Phytochemistry,1997,45(5):1073-1078.

      (責(zé)任編輯:陳翔)

      Study on the triterpenoid constituents in herb of Prunella vulgaris

      CAI Fan1,YAN Qixin2
      (1.Shenzhen Longgang District Maternity&Child Healthcare Hospital,Shenzhen 518172,China;2.Shenzhen Neptunus Bioengineering Co.,Ltd,Shenzhen 518057,China)

      Objective To study the chemical constituents of the herb of Prunella vulgaris.Methods The ethyl acetate part of 80%ethanol extract from the herb of Prunella vulgaris was isolated by silica gel chromatography,LH-20,basin chromatography,and the structures were identified by UV,IR and NMR. Results Seven triterpenoids were isolated and identified as ursolic acid(1),1β,3β-dihydroxyurs-12-en-28-oic acid(2),2α,3β-dihydroxyurs-12-en-28-oic acid(3),3-O-α-L-arabinophyranose-19α-hydroxylurs-12-en-28-oic acid(4),3β,23-dihydroxyurs-12-en-28-oic acid(5),2α,3β,19α,23β-tetrahydroxyurs-12-en-28-oic acid(6),3α,19α,23,24-tetrahydroxyurs-12-en-28-oic acid(7).Conclusion Compounds 2,4-7 were isolated from Prunella vulgaris for the first time.

      Prunella vulgaris;chemical constituents;triterpenoids

      藥物化學(xué)

      R284.2

      A

      1006-8783(2016)04-0428-03

      10.16809/j.cnki.1006-8783.2016050601

      2016-05-06

      蔡凡(1978—),男,主管中藥師,本科,從事臨床藥學(xué)研究工作,Email:caifang16@163.com;通信作者:嚴(yán)啟新(1971—),男,博士,副研究員,副主任藥師,從事新藥研究與開發(fā)工作,Email:yanqixin2005@126.com。

      網(wǎng)絡(luò)出版時間:2016-07-011 14:49 網(wǎng)絡(luò)出版地址:http://www.cnki.net/kcms/detail/44.1413.R.20160711.1449.004.html

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