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      硬毛地筍化學(xué)成分研究

      2013-02-14 12:09:08張前軍康文藝
      關(guān)鍵詞:醋酸乙酯石油醚硅膠

      彭 濤,王 微,張前軍,康文藝*

      1河南大學(xué)中藥研究所,開封475004;2貴州大學(xué)化學(xué)化工學(xué)院,貴陽550025

      硬毛地筍(Lycopus lucidus var.Hirtus)為唇形科地筍屬多年生草本植物,又名硬毛地瓜兒苗,廣泛分布于我國(guó)大部分地區(qū)。地筍屬全世界約有14 種,廣布于東半球溫帶及北美,我國(guó)產(chǎn)4 種4 變種(地筍、硬毛地筍、異葉地筍、小葉地筍、西南小葉地筍、歐地筍、深裂歐地筍和小花地筍)。其味甘、辛、性平,全草入藥,是用于活血化瘀的傳統(tǒng)草藥,根莖可食。它也可用于婦女閉經(jīng),痛經(jīng),產(chǎn)后瘀滯腹痛,身面浮腫等的治療[1,2]。

      作者持續(xù)對(duì)硬毛地筍進(jìn)行系統(tǒng)性的研究[3,4],從硬毛地筍甲醇提取物中分離鑒定了9 個(gè)化合物。其中,化合物4,7 和9 為首次從該科植物中分離得到,1~9 為首次從該植物中分離得到。

      1 材料

      旋轉(zhuǎn)蒸發(fā)儀(日本東京理化);Bruker Am-400超導(dǎo)核磁共振儀;HPMS5973 質(zhì)譜儀(美國(guó)HP 公司);中壓制備柱色譜(上海利穗科技有限公司);X-4 數(shù)字顯示顯微熔點(diǎn)測(cè)定儀(溫度未校正,北京泰克儀器有限公司);GF254硅膠板(煙臺(tái)匯友硅膠開發(fā)有限公司);200~300 目硅膠及硅膠H(青島海洋化工廠出品);Sephadex LH-20(瑞典Pharmacia 公司);ODS(日本Daiso 公司);RP-18(德國(guó)Merck 公司)。柱色譜用氯仿、乙酸乙酯、甲醇和丙酮等試劑均為分析純。

      硬毛地筍于2010 年7 月采集于湖北大別山地區(qū),經(jīng)河南大學(xué)藥學(xué)院中藥研究所生藥教研室李昌勤鑒定為唇形科地筍屬植物硬毛地筍Lycopus lucidus var.hirtus Regel,標(biāo)本存放于河南大學(xué)中藥研究所。

      2 提取和分離

      硬毛地筍全草陰干粉碎(18 kg),室溫下甲醇下冷浸提取3 次,每次3 d。減壓回收甲醇,得甲醇提取物1370 g。將提取物混懸于水后,依次用石油醚、醋酸乙酯、正丁醇萃取,減壓回收溶劑,得石油醚部位、醋酸乙酯部位和正丁醇部位。石油醚部位(200 g)硅膠(200~300 目)常壓柱色譜,石油醚:醋酸乙酯(100∶0~0∶100)梯度洗脫,以TLC 檢測(cè)合并。各部分再經(jīng)過反復(fù)硅膠H,Sephadex LH-20 柱色譜和中壓制備柱色譜分離得到化合物1 (8 mg),2(11 mg),3(20 g),4(15 mg),5(9 mg),6(30 mg)。醋酸乙酯部位(110 g)硅膠(200~300 目)常壓柱色譜。氯仿:丙酮(100∶1~7∶3)梯度洗脫,以TLC 檢測(cè)合并。各部分再經(jīng)過反復(fù)硅膠H,Sephadex LH-20 柱色譜和中壓制備柱色譜分離得到化合物7(7 mg),8(14 mg)和9(45 mg),

      3 結(jié)構(gòu)鑒定

      化合物1 紫紅色片晶(石油醚);mp:176~178 ℃;EI-MS m/z:536 [M]+,444,430,397,378,333,281,268,209,195,173,159,145,132,119,105,91,69,56,43。與β-胡蘿卜素標(biāo)準(zhǔn)品在三種不同溶劑系統(tǒng)中Rf值及斑點(diǎn)顏色一致,相互混合熔點(diǎn)不下降,故鑒定為β-胡蘿卜素。

      化合物2 淡黃色針晶(石油醚-醋酸乙酯);mp:324~326 ℃;EI-MS m/z:272 [M]+,161,178,133.1H NMR (CDCl3,400 MHz)δ:8.01 (1H,d,J=8.6 Hz,H-5),7.48 (1H,br s,H-2'),7.45 (1H,d,J=8.6 Hz,H-6'),6.96 (1H,br d,J=8.6 Hz,H-5'),6.58 (1H,br s,H-6),6.39 (1H,br s,H-8);13C NMR (CDCl3,100 MHz)δ:180.4 (C = O),165.7(C-2),103.8(C-3),127.8(C-5),114.2(C-6),165.3(C-7),105.2(C-8),157.8(C-9),116.6(C-10),124.1 (C-1'),116.5 (C-2'),147.2 (C-3'),151.0(C-4'),116.9(C-5'),120.2(C-6')。以上數(shù)據(jù)與文獻(xiàn)[5]報(bào)道基本一致,故鑒定為7,3',4'-三羥基黃酮。

      化合物3 白色片晶(石油醚-醋酸乙酯);mp:137~138 ℃;EI-MS m/z:414[M]+,396,381,329,303,255,213,145,55。與文獻(xiàn)報(bào)道的β-谷甾醇EIMS 一致[6],與β-谷甾醇標(biāo)準(zhǔn)品在三種不同溶劑系統(tǒng)中Rf值及斑點(diǎn)顏色一致,相互混合熔點(diǎn)不下降,故鑒定為β-谷甾醇。

      化合物4 黃色粉末(氯仿-丙酮);mp:234~236 ℃;EI-MS m/z:330[M]+,301,287;1H NMR(CDCl3,400 MHz)δ:7.75(1H,d,J = 2.4 Hz,H-2'),7.66(1H,dd,J=2.4,9.0 Hz,H-6'),6.96(1H,d,J=9.0 Hz,H-5'),6.86(1H,d,J =2.2 Hz,H-8),6.33 (1H,d,J = 1.5 Hz,H-6),3.96(3H,s,7-OCH3),3.87(3H,s,3-OCH3);13C NMR (CDCl3,100 MHz)δ:56.0(7-OCH3),59.6(3-OCH3),155.9(C-2),137.8(C-3),177.9(C-4),156.2(C-5),97.6(C-6),165.0(C-7),92.1(C-8),160.9(C-9),105.1(C-10),120.6(C-1'),115.4(C-2'),145.3(C-3'),149.0(C-4'),115.6(C-5'),120.4(C-6')。以上數(shù)據(jù)與文獻(xiàn)[7]報(bào)道基本一致,故鑒定為3',4',5-三羥基-3,7-二甲氧基黃酮。

      化合物5 白色針晶(石油醚-醋酸乙酯);mp:154~156 ℃;EI-MS m/z:426[M]+;1H NMR(CDCl3,400 MHz)δ:5.13(1 H,t,J = 3.5 Hz ,H-12),4.78(1H,br s,H-30b),3.23 (1H,dd ,J =5.0,10.5 Hz ,H-3),0.91(3H,d,J = 6.0 Hz),0.86(3H,d,J =6.0Hz),1.33,1.28,1.20,1.11,1.06,1.03(each 3H,s,6 × CH3);13C NMR (CDCl3,100 MHz)δ:38.7(C-1),27.2(C-2),79.0(C-3),38.7(C-4),55.1(C-5),18.3(C-6),32.9(C-7),39.9(C-8),47.7(C-9),36.9(C-10),23.3(C-11),124.4(C-12),139.5(C-13),42.1(C-14),28.7(C-15),26.6(C-16),33.7(C-17),59.0(C-18),39.6(C-19),39.6(C-20),31.2(C-21),41.5(C-22),28.1(C-23), 15.7(C-24),15.6(C-25),16.9(C-26),23.2(C-27),29.7(C-28),17.5(C-29),21.3(C-30)。以上數(shù)據(jù)與文獻(xiàn)[8]報(bào)道基本一致,故鑒定為α-香樹脂醇。

      化合物6 白色針晶(石油醚-醋酸乙酯);mp:197~199 ℃;EI-MS m/z:426[M]+,411,218,203,189;1H NMR (CDCl3,400 MHz)δ:5.18(1H,t,J =4.8Hz,H-12),3.22(1H,t ,J = 6.9 Hz,H-3),1.13(3H,s,H-27),1.07(3H,s,H-23),1.00(3H,s,H-25),0.97(3H,s,H-24),0.94(3H,s,H-29),0.87(3H,s,H-30),0.83(3H,s,H-28),0.79 (3H,s,H-26);13C NMR (CDCl3,100 MHz)δ:38.2(C-1),28.3(C-2),78.6(C-3),38.6(C-4),51.1(C-5),19.2(C-6),31.3(C-7),39.8(C-8),46.7(C-9),38.5(C-10),24.8(C-11),123.6(C-12),141.7(C-13),43.6(C-14),28.3(C-15),28.0(C-16),32.3(C-17),37.0(C-18),36.5(C-19),32.2(C-20),35.7(C-21),36.2(C-22),27.1(C-23),16.5(C-24),16.5(C-25),17.7(C-26),28.9(C-27),28.7(C-28),33.4(C-29),24.6(C-30)。以上數(shù)據(jù)與文獻(xiàn)[9]報(bào)道基本一致,故鑒定為β-香樹脂醇。

      化合物7 白色粉末(氯仿-甲醇);mp:276~278 ℃;EI-MS m/z:442 [M]+,436,426,408,393,300,248,223,203,189,175,133;1H NMR (Pyridined5,400 MHz)δ:5.12(1H,m,H-12),3.83(1H,d,J=10.91 Hz,H-24),3.17(1H,br d,J =9.76 Hz,H-24),2.11(1H,d,J =11.20 Hz,H-18),1.46(H,br s,Ha-3),1.24(H,br s,Hb-3),1.06(3H,s,H-27),10.4(3H,s,H-23),1.03(3H,s,H-26),0.86(3H,d,J = 5.37 Hz,H-30),0.81(3H,d,J = 6.30 Hz,H-29),0.72(3H,s,H-25);13C NMR (Pyridine-d5,100 MHz)δ:39.1(C-1),27.9(C-2),39.5(C-3),43.1(C-4),48.7(C-5),18.7(C-6),33.4(C-7),40.1(C-8),48.2(C-9),37.3(C-10),23.8(C-11),125.8(C-12),139.5(C-13),42.6(C-14),28.9(C-15),25.1(C-16),48.4(C-17),53.9(C-18),39.4(C-19),39.6(C-20),31.8(C-21),37.5(C-22),14.3(C-23),68.7(C-24),16.7(C-25),17.3(C-26)24.9(C-27),181.3(C-28),17.1(C-29),21.5(C-30)。綜合各數(shù)據(jù)及與文獻(xiàn)[10]對(duì)比鑒定化合物為24-羥基-烏蘇-12-烯-28-酸。

      化合物8 白色無定形粉末(氯仿-甲醇);mp:297~299 ℃;與β-胡蘿卜苷標(biāo)準(zhǔn)品在三種不同溶劑系統(tǒng)中Rf值及斑點(diǎn)顏色一致,相互混合熔點(diǎn)不下降,故鑒定為β-胡蘿卜苷。

      化合物9 白色粉末(氯仿-甲醇);mp:317~319 ℃;EI-MS m/z:576 [M]+,526,481,414,396,382,329,303,288,275,255,231,199,159,145,105,83,57,43;1H NMR (Pyridine-d5,400 MHz)δ:6.47(1H,br s,-OH),5.35(1H,s,H-7),5.22(1H,dd,J=11.6 Hz,H-22),5.09(1H,dd,J =10.8,11.6 Hz,H-23),4.60(1H,dd,J = 2.0,2.4 Hz,Glc-H-1),4.43(1H,dd,J=7.2,6.8 Hz,Glc-H-5),4.34~4.26(2H,m,Glc-H-6),4.07(1H,t,J =12.0 Hz,Glc-H-4),3.96-3.92(2H,m,Glc-H-2,3),2.76(1H,dd,J =3.6,4.0 Hz,H-3),2.48(1H,t,J =15.6 Hz,H-21 or 24),2.13(1H,b d,J =13.2 Hz,H-14),2.00-1.07(18H,m,H-1~26),1.01(3H,s,H-20),0.95(3H,s,H-27),0.91(3H,s,H-28),0.88(3H,s,H-19),0.67(3H,s,H-18);13C NMR (Pyridine-d5,100 MHz)δ:40.3(C-1),39.7(C-2),72.0(C-3),37.3(C-4),50.7(C-5),63.2(C-6),122.3(C-7),141.2(C-8),46.4(C-9),42.8(C-10),30.6(C-11),41.1(C-12),36.7(C-13),51.8(C-14),34.6(C-15),32.6(C-16),56.4(C-17),26.7(C-18),24.9(C-19),20.3(C-20),33.0(C-21),129.8(C-22),139.2(C-23),37.8(C-24),28.9(C-25),23.7(C-26),21.7(C-27),19.4(C-28),102.9(C-1'),78.9(C-5'),78.8(C-3'),78.4(C-2'),75.7(C-4'),57.2(C-6')。綜合各數(shù)據(jù)及與文獻(xiàn)[11,12]對(duì)比鑒定化合物為24-甲基-5α-膽甾-7,22-二烯-6α-醇-3β-O-葡萄糖苷。

      1 Editorial Committee of Flora of China.Flora of China(中國(guó)植物志).Beijing:Science Press,1995,66:274-278.

      2 Editorial Committee of Chinese Herb(中華本草).第七冊(cè)十九.Shanghai:Science Press,1999,19:6091-6095.

      3 Peng T(彭濤),Yin ZH(尹震花),Kang WY(康文藝),et al.Analysis of fat-soluble components in Lycopus lucidus by GC-MS.Chin J Experimental Tradit Med Formulae(中國(guó)實(shí)驗(yàn)方劑學(xué)雜志),2011,17:100-102.

      4 Peng T(彭濤),Wang JM(王金梅),Zhang QJ(張前軍),et al. Volatile oils constituents of Lycopus lucidus var. hirtus.Nat Prod Res Dev(天然產(chǎn)物研究與開發(fā)),2012,24:342-344.

      5 Frederique Van Acker AA,Hageman Jos A,Haenen Guidor MM et al. Synthesis of novel 3,7-substituted-2-(3',4'-dihydroxyphenyl)flavones with improved antioxidant activity.J Med Chem,2000,43:3752-3760.

      6 Cong PZ(叢浦珠),Li SY(李筍玉).Natural Organic Mass Spectral.Beijing:Chinses Medical Science Publishing Press,2003.1136.

      7 Li Q(李欽),Shen YM(沈月毛),Li P(李萍). Study on flavanoids in the leaves of Premnaszem aoensis Pei. Chin Pharm J(中國(guó)藥學(xué)雜志),2008,43:417-419.

      8 Li WW(李薇薇),Shi MH(史海明),Wang MY(王夢(mèng)月),et al.Chemical constituents of Viburnum erosum var.erosum and Viburnum odoratissimum var.awabuki.Chin Pharm J(中國(guó)藥學(xué)雜志),2011,46:1234-1237.

      9 Li CK(李傳寬),Zhang QJ(張前軍),Huang ZB(黃鐘碧),et al. Chemical constituents of Desmodium sambuense.China J Chin Mater Med(中國(guó)中藥雜志),2010,35:2420-2423.

      10 Hou WL,Li YF,Zhang Q,et al. Triterpene acids isolated from Lagerstroemia speciosa leaves as α-Glucosidase inhibitors.Phytotherapy Reseach,2009,23:614-618.

      11 Madaio A,Piccialli V,Sica D,et al. New polyhydroxysterols from the dictyoceratid sponges Hippospongia Communis,Spongia Officinalis,Ircinia Variabilis,and Spongionella Gracilis.J Nat Prod,1989,52:952-961.

      12 Yoshihisa Takaishi,Minoru Uda,Takashi Ohashi,et al. Glycosides of ergosterol derivatives from Hericum Erinacens.Phytochemistry,1991,30:4117-4120.

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