王智慧,凌鐵軍,張 梁,鮑官虎,孫啟祥,張 倩,汪小剛,方從兵*
1安徽農(nóng)業(yè)大學(xué)茶葉生物化學(xué)與生物技術(shù)教育部重點(diǎn)實(shí)驗(yàn)室,合肥 230036;2 中國(guó)林業(yè)科學(xué)研究院林業(yè)研究所國(guó)家林業(yè)局林木培育重點(diǎn)實(shí)驗(yàn)室,北京 100091
樟樹(Cinnamomum camphora)是樟科(Lauraceae)樟屬植物,別名:香樟、樟木、芳樟、烏樟、油樟、香蕊、小葉樟,系常綠喬木[1]。樟樹分布廣泛,主產(chǎn)于我國(guó)南方各省區(qū),以福建、臺(tái)灣為最多,為熱帶和亞熱帶常綠闊葉林的代表樹種,被譽(yù)為江南寶樹。樟樹的化學(xué)成分主要有揮發(fā)油、黃酮類、生物堿、有機(jī)酸、木脂素及核糖體失活蛋白等,樟樹的莖、葉、根、果實(shí)、種子等各部分都具有一定的生物活性,主要涉及抑菌[2,3]、食品防腐保鮮[4,5]、驅(qū)蟲[6,7]、抗氧化[8]、消炎及細(xì)胞毒活性[9]等方面,在臨床醫(yī)學(xué)應(yīng)用上也越來越常見[10,11]。
目前,對(duì)樟樹的研究大多集中在揮發(fā)油的化學(xué)成分檢測(cè)分析和粗提物生物活性方面,而對(duì)于樟樹葉片中非揮發(fā)性成分的化學(xué)組成相關(guān)報(bào)道較少。本文以干燥處理的樟樹葉為材料,經(jīng)過醇提、萃取、柱層析對(duì)樟樹葉中有效的非揮發(fā)性成分進(jìn)行分離及結(jié)構(gòu)鑒定,共分離和鑒定出9個(gè)化合物,最后與已知文獻(xiàn)數(shù)據(jù)對(duì)照,確證化合物結(jié)構(gòu)。分別為山柰酚-3-O-β-D-葡萄糖苷(1),槲皮素-3-O-β-D-鼠李糖苷(2),槲皮素-3-O-β-D-葡萄糖苷(3),異鼠李素-3-Oβ-D-葡萄糖苷(4),黑色五味子單體苷(5),山奈酚-3-O-β-D-蕓香糖苷(6),異鼠李素-3-O-β-D-蕓香糖苷(7),新芝麻脂素(8)和maculatin(9)。其中,化合物1 為首次從樟屬中分離得到,化合物4、5 和8 為首次從樟科植物中分離得到。
樟樹葉采自安徽合肥市苗圃,經(jīng)安徽農(nóng)業(yè)大學(xué)林學(xué)與園林學(xué)院黃成林教授鑒定為Cinamomum camphora 的樹葉。
核磁共振波譜儀(美國(guó)BROKER 公司,400 MHz1H NMR,100 MHz13C NMR),旋轉(zhuǎn)蒸發(fā)器(上海申勝生物技術(shù)有限公司R-201 型),核磁測(cè)試用氘代試劑DMSO、氯仿、甲醇(美國(guó)CIL 公司),電子天平(上海天平儀器廠T6328B 型),電熱鼓風(fēng)干燥箱(上海一恒科技有限公司),實(shí)驗(yàn)試劑為分析純(天津博迪有限公司),硅膠(柱層析用,100~200、200~300、300~400 目,青島海洋化工廠分廠),葡聚糖凝膠(Sephadex LH-20,美國(guó)Pharmacia 公司),聚酰胺粉(國(guó)藥集團(tuán)化學(xué)試劑有限公司),聚酰胺薄膜(國(guó)藥集團(tuán)化學(xué)試劑有限公司)。
將8.4 kg 烘干樟樹葉全部粉碎,用甲醇浸提3次,得750 g 樟樹葉甲醇粗提浸膏,依次采用石油醚、氯仿、正丁醇3 種不同極性的有機(jī)試劑分級(jí)萃取,得到石油醚部分(100 g)、氯仿部分(45 g)、正丁醇部分(160 g)及水相4個(gè)部分的分級(jí)萃取物浸膏。
正丁醇浸膏(160 g)經(jīng)HPD-500 型大孔樹脂層析柱,得到Ⅰ~Ⅴ五個(gè)部分。部分II(51.7 g)濕法過硅膠柱,乙酸乙酯-甲醇-水(10∶0.5∶0.5→6∶0.5∶0.5→2∶0.5∶0.5)梯度洗脫得到組分1~13。組分2(2.7 g),依次通過過硅膠柱(乙酸乙酯-甲醇-水)、聚酰胺柱(二氯甲烷-甲醇)梯度洗脫,得到化合物1(15 mg)和化合物2(39 mg)。組分3(1.5 g),上聚酰胺柱,用二氯甲烷-甲醇(4∶1)洗脫劑洗脫,得化合物3(10 mg)和化合物4(16 mg)。組分4(約200 mg)有白色化合物析出,抽濾得白色沉淀部分,過凝膠柱得到化合物5(10 mg)。組分7(3.2 g),濕法過硅膠柱,氯仿-甲醇-水(15∶1∶0.1→10∶1∶0.1→7∶1∶0.1→7∶3∶0.5)梯度洗脫,得化合物6(40 mg)。組分8(1.6g),濕法過硅膠柱,二氯甲烷-甲醇-水(15∶1∶0.1→10∶1∶0.1→7∶1;0.1→8;2∶0.3)梯度洗脫,得化合物7(35 mg)。
氯仿浸膏(45 g),濕法過硅膠柱,丙酮-石油醚(6∶1→4∶1→2∶1→1∶1)梯度洗脫,得化合物8(50 mg)和化合物9(100 mg)。
化合物1 黃色粉末(甲醇);EIS-MS m/s:447[M-H]-。1H NMR(DMSO-d6,400 MHz)δ:12.61(1H,s,5-OH),8.05(2H,d,J=8.8 Hz,H-2',6'),6.89(2H,d,J=8.8 Hz,H-3',5'),6.44(1H,d,J=2.0 Hz,H-8),6.21(1H,d,J=2.0 Hz,H-6),5.46(1H,d,J=7.6 Hz,H-1'')。以上數(shù)據(jù)與文獻(xiàn)[12]報(bào)道數(shù)據(jù)一致,故鑒定化合物1 為山柰酚-3-O-β-D-葡萄糖糖苷。
化合物2 黃色粉末(甲醇);EIS-MS m/s:447[M-H]-。1H NMR(DMSO-d6,400 MHz)δ:6.20(1H,d,J=2.0 Hz,H-6),6.39(1H,d,J=2.0 Hz,H-8),7.53(1H,br s,H-2'),6.85(1H,d,J=8.8 Hz,H-5'),7.45(1H,dd,J=2.4,8.8 Hz,H-6'),5.27(1H,br s,H-1''),4.39(1H,d,J=1.2 Hz,H-2''),3.71(1H,d,J=10.4 Hz,H-3''),3.06-3.39(2H,m,H-4'',5''),0.99(3H,d,J=6.4 Hz,H-6'')。以上光譜數(shù)據(jù)與文獻(xiàn)[13]對(duì)照,確定化合物2 為槲皮素-3-O-β-D-鼠李糖苷。
化合物3 黃色固體(甲醇);EIS-MS m/s:463[M-H]-。1H NMR(DMSO-d6,400 MHz)δ:7.59(1H,dd,J=2.0,8.8 Hz,H-6'),7.59(1H,d,J=2.4 Hz,H-2'),6.87(1H,d,J=8.4 Hz,H-5'),6.39(1H,d,J=2.4 Hz,H-8),6.20(1H,d,J=2.0 Hz,H-6),5.25(1H,d,J=7.6 Hz,H-l'')。以上數(shù)據(jù)與文獻(xiàn)[14]中槲皮素-3-O-β-D-葡萄糖苷一致,故鑒定化合物3 為槲皮素-3-O-β-D-葡萄糖苷。
化合物4 黃色粉末(甲醇);EIS-MS m/s:477[M-H]-。1H NMR(DMSO-d6,400 MHz)δ:12.62(1H,s,5-OH),7.95(1H,d,J=2.0 Hz,H-2'),7.51(1H,dd,J=2.0,8.4 Hz,H-6'),6.92(1H,d,J=8.4 Hz,H-5'),6.45(1H,d,J=2.0 Hz,H-8),6.22(1H,d,J=2.0 Hz,H-6),5.57(1H,d,J=7.2 Hz,H-1''),3.85(3H,s,3'-OCH3);13C NMR(DMSO-d6,100 Hz)δ:177.4(C-4),164.2(C-7),161.2(C-5),156.4(C-9),156.2(C-2),149.4(C-4'),146.9(C-3'),133.0(C-3),122.0(C-1'),121.1(C-6'),115.2(C-5'),113.5(C-2'),104.0(C-10),100.8(C-1''),98.7(C-6),93.7(C-8),77.4(C-5''),76.4(C-3''),74.3(C-2''),69.8(C-4''),60.6(C-6''),55.7(3'-OCH3)。以上數(shù)據(jù)與文獻(xiàn)[12,15]報(bào)道數(shù)據(jù)基本一致,故鑒定化合物4 為異鼠李素-3-Oβ-D-葡萄糖苷。
化合物5 白色無定型粉末(甲醇);EIS-MS m/s:515[M +Na]+。1H NMR(CD3OD,400 MHz)δ:6.77(1H,d,J=2.0 Hz,H-2),6.74(1H,d,J=8.0 Hz,H-6),6.65(1H,s,H-2'),6.62(1H,dd,J=2.0 Hz,8.0 Hz,H-5),6.16(1H,d,J=0.4 Hz,H-5'),4.05(1H,d,J=10.4 Hz,H-9a)*,4.04(1H,d,J=7.2 Hz,H-1''),3.97(1H,dd,J=2.4,9.6 Hz,H-9'a),3.80(3H,s,3-OCH3),3.79(3H,s,3'-OCH3),3.79(1H,m,H-5''a)*,3.75(1H,dd,J=4.0,11.2 Hz,H-9b),3.69(1H,dd,J=6.0,10.8 Hz,H-9'b),3.45(1H,m,H-4'),3.17-3.27(3H,m,H-7),3.11(1H,t,J=11.2 Hz,H-2'),2.82(2H,m,H-7'),2.06(1H,m,H-8),1.85(1H,tt,J=2.8,10.8 Hz,H-8');13C NMR(CD3OD,100 MHz):134.4(C-1),114.3(C-2),147.2(C-3),145.2(C-4),116.1(C-5),123.2(C-6),48.0(C-7),45.9(C-8),69.6(C-9),129.1(C-1'),112.5(C-2'),149.0(C-3''),145.9(C-4'),117.4(C-5'),138.6(C-6''),33.8(C-7'),39.7(C-8'),66.9(C-9'),105.8(C-1''),78.0(C-2''),75.0(C-3''),71.3(C-4''),65.2(C-5''),56.5(3-OCH3),56.4(3'-OCH3)。以上數(shù)據(jù)與文獻(xiàn)報(bào)道[16]的黑色五味子單體苷數(shù)據(jù)對(duì)照,基本一致,確定化合物5 為黑色五味子單體苷。
化合物6 黃色固體(甲醇);EIS-MS m/s:593[M-H]-。1H NMR(DMSO-d6,400 MHz)δ:12.56(1H,s,5-OH),10.32(1H,s,7-OH),10.10(1H,s,4'-OH),7.98(2H,d,J=8.8 Hz,H-2',6'),6.88(2H,d,J=8.8 Hz,H-3',5'),6.41(1H,d,J=2.0 Hz,H-8),6.21(1H,d,J=2.0 Hz,H-6),5.3l(1H,d,J=7.2 Hz,H-l''),4.37(1H,d,J=1.2 Hz,H-1'''),3.01-3.70(4H,m,sugar protons),0.98(3H,d,J=6.4 Hz,H-6''');13C NMR (DMSO-d6,100 MHz):157.3 (C-2),133.7 (C-3),178.0 (C-4),161.6(C-5),99.1(C-6),164.6(C-7),94.2(C-8),157.0(C-9),104.3(C-10),121.4(C-1'),131.4(C-2',6'),115.6(C-3',5'),160.3(C-4'),101.3(C-1''),74.6(C-2''),76.8(C-3''),70.8(C-4''),76.2(C-5''),67.3 (C-6''),101.2 (C-1'''),71.1 (C-2'''),70.4(C-3'''),72.2(C-4'''),68.7(C-5'''),18.2(C-6''')。以上數(shù)據(jù)與文獻(xiàn)[12,17]報(bào)道數(shù)據(jù)基本一致。故鑒定化合物6 為山柰酚-3-O-β-D-蕓香糖苷。
化合物7 黃色固體(甲醇);EIS-MS m/s:623[M-H]-。1H NMR(DMSO-d6,400 MHz)δ:12.57(1H,s,5-OH),7.85(1H,d,J=2.0 Hz,H-2'),7.50(1H,dd,J=2.0,8.4 Hz,H-6'),6.91(1H,d,J=8.4 Hz,H-5'),6.43(1H,d,J=2.0 Hz,H-8),6.20(1H,d,J=2.0 Hz,H-6),5.43(1H,d,J=7.2 Hz,H-1''),4.49(1H,br s,H-1'''),3.84(3H,s,3'-OCH3),3.01-3.72(3H,m,sugar protons),0.98(3H,d,J=6.0 Hz,H-6''');13C NMR(DMSO-d6,100 MHz)δ:17.6(C-6'''),55.6(3'-OCH3),66.8(C-6''),68.2 (C-5'''),70.1 (C-3'''),70.3 (C-2'''),70.6(C-4'''),71.8(C-4'''),74.2(C-2''),75.9(C-3''),76.4(C-5''),93.8(C-8),98.7(C-6),100.8(C-1'''),101.1(C-1''),104.0(C-10),113.3(C-2'),115.2(C-5'),121.0(C-1'),122.3(C-6'),133.0(C-3),146.9(C-4'),149.4(C-3'),156.4(C-2,9),161.2(C-5),164.1(C-7),177.3(C-4)。以上數(shù)據(jù)與文獻(xiàn)[18,19]報(bào)道數(shù)據(jù)基本一致,故鑒定化合物7為異鼠李素-3-O-β-D-蕓香糖苷。
化合物8 無色針狀晶體(甲醇);EIS-MS m/s:375[M+Na]+。1H NMR(CDCl3,400 MHz)δ:6.76~6.88(6H,m,H-Ar),5.95(4H,s,2(-OCH2O-)),5.94(1H,s,H-4β),4.95(1H,d,J=6.8 Hz,H-2),4.83(1H,d,J=7.2 Hz,H-6),4.23(1H,dd,J=6.0,9.2 Hz,H-8β),4.01(1H,dd,J=2.4,9.2 Hz,H-8α),3.23(1H,m,H-1),2.97(1H,m,H-5);13C NMR(CDCl3,100 MHz)δ:54.80(C-1,5),72.79(C-8),84.12 (C-6),87.99 (C-2),101.90 (C-2 (-OCH2O)),102.53(C-4),107.03(C-2'),107.77(C-2''),108.43(C-5'),108.78(C-5'),120.26(C-6'),120.42 (C-6''),137.66 (C-1'),138.56 (C-1''),147.77 (C-3'),147.94 (C-3''),148.74 (C-4'),148.91(C-4'')。上述波譜數(shù)據(jù)與文獻(xiàn)[20]一致,故鑒定化合物8 為新芝麻脂素。
化合物9 白色晶體(甲醇);EIS-MS m/s:409[M+Na]+。1H NMR(CDCl3,400 MHz)δ:6.77(1H,d,J=8.0 Hz,H-5),6.75(1H,d,J=7.6 Hz,H-5'),6.69(1H,d,J=2.0 Hz,H-2),6.66(1H,dd,J=2.0,8.0 Hz,H-6),6.55(1H,dd,J=2.0,8.0 Hz,H-6'),6.49(1H,d,J=2.0 Hz,H-2'),4.12(1H,dd,J=7.2,9.2 Hz,H-9'β),3.87(1H,dd,J=1.6,3.6 Hz,H-9'α)*,3.86(3H,s,3-OCH3),3.85(3H,s,3'-OCH3),3.84(3H,s,4-OCH3),3.82(3H,s,4'-OCH3),2.64(1H,m,H-7'β),2.58(1H,m,H-8),2.53(1H,m,H-7'α),2.48(1H,m,H-8'),2.93(1H,dd,J=6.4,14.0 Hz,H-7α),2.97(1H,dd,J=6.0,14.0 Hz,H-7β);13C NMR(DMSO-d6,100 MHz):178.68(C-9),149.17(C-3),149.04(C-3'),147.95(C-4),147.82(C-4'),131.68(C-1),131.03(C-1'),121.72(C-6),120.88(C-6'),113.65(C-2),112.89(C-2'),112.34(C-5),112.20(C-5'),71.17 (C-9'),55.94 (4-OCH3),55.92 (4' -OCH3),55.88(3-OCH3),55.82(3' -OCH3),46.09(C-8),41.26(C-8'),37.38(C-7'),34.14(C-7)。上述波譜數(shù)據(jù)與文獻(xiàn)[21,22]一致,確定化合物9 為maculatin。
* :有信號(hào)覆蓋。
1 Tao GF(陶光復(fù)),Phytochemical resources of camphor oils in Hubei,China.Resources and Environment in The Yangtze Basin(長(zhǎng)江流域資源與環(huán)境),2003,12:124-129.
2 Li AM(李愛民),Tang YQ(唐永勤),Qing YB(卿玉波).Study on the extraction and antimicrobial activity of camphor oil.J Fujian Forestry Sci Tech(福建林業(yè)科技),2006,33:121-123.
3 Hu RH(胡仁火),Ren GY(任國(guó)祥),Xu H(徐輝),et al.The inhibitory and bactericidal effect of the 8 campus green plants'volatile substances.J Anhui Agri Sci(安徽農(nóng)業(yè)科學(xué)),2007,35:9128-9129.
4 Wen CF(文赤夫),Zeng CW(曾超文),Huang ZC(黃早成),et al.The antibacterial activity of the red pigment in the fruit of Cinnamomum camphora.Food and Fermentation Industries(食品發(fā)酵與工業(yè)),2007,33(4):23-25.
5 Lu LB(盧凌彬),Meng F(孟方).Study on the new fruit and vegetable's preservative.Guangzhou Chem(廣州化學(xué)),2002,27(3):33-36.
6 Zhou Q(周瓊),Liang GW(梁廣文).Plant ethanol extraction affects on vegetable aphids and aphid parasitoids.Chin J App Eco(應(yīng)用生態(tài)學(xué)報(bào)),2003,14:249-252.
7 Yao AQ(姚安慶),Liang DH(梁德華).The biological activity on cabbage butterfly larvae of of the extract from Cinnamomum camphora and Hemerocallis citrina Baroni.Mod Agr(現(xiàn)代農(nóng)藥),2004,3(2):28-29.
8 Lee HJ,Hyun EA,Yoon WJ,et al.In vitro anti-inflammatory and anti-oxidative effects of Cinnamomum camphora extracts.J Ethnopharmacol,2006,103:208-216.
9 Ling J,Liu WY.Cytotoxicity of two new ribosome-inactivating proteins,cinnamomin and camphorin,to carcinoma cells.Cell Biochem Funct,1996,14:157-161.
10 Kim SI,Na YE,Yi JH,et al.Contact and fumigant toxicity of oriental medicinal plant extracts against Dermanyssus gallinae(Acari:Dermanyssidae).Vet Parasitol,2007,145:377-382.
11 El-Shazly AM,Hassan AA,Soliman M,et al.Treatment of human Demodex folliculorum by camphor oil and metronidazole.J Egypt Soc Parasitol,2004,34:107-116.
12 Yi Y(易衍),Wu X(巫鑫),Wang Y(王英),et al.Study on the flavonoids from Rafflesia arnoldii.J Chin Med Mat(中藥材),2011,34:712-716.
13 Wang KJ(王開金),Chen LZ(陳列忠),Li N(李寧),et al.The antioxidant and radical scavenging activity of flavonoids from Solidago canadensis.Chin Pharm J(中國(guó)藥學(xué)雜志),2006,41:493-497.
14 Ma L(馬麟),Zhou HL(周海玲),Gong YM(龔又明),et al.Study on flavonoids from Artemisia lavandulaefolia.Tradi Chin Dru Rese Clin Phar(中藥新藥與臨床藥理),2012,23:555-578.
15 Chen Y(陳雨),F(xiàn)eng X(馮煦),Jia XD(賈曉東),et al.Chemical constituents in the bud of Lonicera macranthoides Hand.-Mazz.Chin Tradit Herb Drugs(中草藥),2008,39:823-825.
16 Dong L(董禮),Chen M(陳敏),Li M(李梅),et al.A new cyanogenic glycosides from Rhodiola bupleuroides.Acta Pharmaceutica Sinic,(藥學(xué)學(xué)報(bào)),2009,44:1383-1386.
17 Fu W(付偉),Lei YF(雷永芳),Zhou DN(周道年),et al.Study on flavonoids from Parathelypteris nipponica.Chin Pharm J(中國(guó)藥學(xué)雜志),2010,45:166-168.
18 Liu H(劉浩),Zhao JL(趙江林),Lv SQ(呂仕瓊),et al.Flavonoids from Halostachys caspica and their antimicrobial and antioxidant activities.中國(guó)科技論文在線(http://www.paper.edu.cn)
19 Feng SX(馮世秀),Liu MF(劉梅芳),Wei XY(魏孝義),et al.Study on triterpenoids and flavonoids from Microcos paniculata Linn.J Trop Subtrop Botany(熱帶亞熱帶植物學(xué)報(bào)),2008,16:51-56.
20 Wang Z(王展),He ZS(何直昇).Studies on the chemical constituents of the seeds of Chinese dodder(Cuscuta chinensis).Chin Tradit Herb Drugs(中草藥),1998,29:577-579.
21 Chimichi S,Cosirnelli B.Complete1H(600 MHz)and13C NMR Spectral Assignments of 3,4-Bis [(3,4-dimethoxyphenyl)-methyl]dihydro-(3R-trans)-2 (3H)-furanone (Matairesinol Dimethyl Ether),a naturally occurring dibenzylbutyrolactone lignan.Magn reson chem,1993,31,1044-1047
22 Liao MC(廖矛川),Yang FY(楊芳云),Sha GP(沙光普),et al.Study on the chemical constituents from the leaves of Cinnamomum camphora.J South-Central Uni.Nat Sci Edi(中南民族大學(xué)學(xué)報(bào),自科版),2012,31(3):52-55.