于 歡，李 敏，張 旭，王玲莉，王 佳，張冬麗，許 嶸，唐生安*

1.天津醫(yī)科大學(xué)藥學(xué)院，天津市臨床藥物關(guān)鍵技術(shù)重點(diǎn)實(shí)驗(yàn)室，天津 300070

2.泉州醫(yī)學(xué)高等專科學(xué)校藥學(xué)院，福建 泉州 362011

藍(lán)桉Eucalyptus globulusLabill.為桃金娘科（Myrtaceae）桉屬EucalyptusL.Herit植物，原產(chǎn)于澳大利亞，在我國廣西、云南、四川等地均有栽培，其葉、根皮及果實(shí)均可入藥[1-2]，是一種重要的藥用資源。藍(lán)桉的果實(shí)因成熟后其形狀酷似倒掛的“小鐘”又俗稱“一口鐘”，民間俗稱扣子七、紅喇叭花、勝利果等[3]，是我國傳統(tǒng)民間中草藥，也是藍(lán)桉臨床上常用的有效部位。一口鐘富含多種揮發(fā)油、倍半萜、三萜、間苯三酚衍生物、黃酮和鞣質(zhì)等化學(xué)成分[4-5]，具有抗腫瘤、抗菌、抗病毒、抗氧化和降血糖[6]等多種生物活性。

一口鐘在我國分布廣泛，資源豐富。本課題組前期對一口鐘石油醚萃取物進(jìn)行化學(xué)成分研究，發(fā)現(xiàn)其主要含有倍半萜和三萜類化合物[7]，在此基礎(chǔ)上，為了進(jìn)一步探索其活性成分，本實(shí)驗(yàn)繼續(xù)對一口鐘石油醚萃取物進(jìn)行研究，采用硅膠柱色譜、凝膠柱色譜、以及高效液相色譜技術(shù)進(jìn)行分離，采用波譜學(xué)方法與理化性質(zhì)相結(jié)合鑒定了15個(gè)化合物，分別為大黃酚（chrysophanol，1）、eucarobustol E（2）、eucarobustol G（3）、eucalyptal A（4）、eucalyptal C（5）、eucalyptin C（6）、eucalyptin D（7）、eucalyptin E（8）、eucalrobusone A（9）、eucalrobusone C（10）、eucalrobusone F（11）、eucalrobusone U（12）、eucalyptone（13）、euglobal-Ia1（14）、euglobal-Ia2（15）。分離得到的化合物均為酚性成分。其中，化合物1為首次從桉屬植物中分離得到的，化合物2、3為首次從該植物中分離得到，化合物9～15為首次從藍(lán)桉果實(shí)中分離得到。其中化合物6、7、10、12、13對MCF-7細(xì)胞具有明顯細(xì)胞毒活性，20 μmol/L的濃度下抑制率分別為71.83%、71.11%、70.00%、80.53%、79.87%，化合物12對MCF-7顯示出較強(qiáng)的細(xì)胞毒活性，其半數(shù)抑制濃度（IC50）為13.84 μmol/L。

1 儀器與材料

Bruker AM-400/500/600 核磁共振儀（Bruker 公司，瑞士）；Alliance 2695 Quattro Micro TM ESI 液質(zhì)聯(lián)用色譜儀（Waters公司，美國）；LC3000型高效液相色譜儀（北京創(chuàng)新通恒科技有限公司）；YMC-Pack ODS-A制備型HPLC色譜柱（250 mm×20 mm）；Sephadex LH-20（美國GE公司），柱色譜硅膠（100～200、200～300、300～400目）和薄層板色譜硅膠GF254均為青島海洋化工有限公司產(chǎn)品；實(shí)驗(yàn)所用試劑均為分析純有機(jī)試劑，為天津市津東天正精細(xì)化學(xué)試劑廠產(chǎn)品；氘代試劑均為Cambrige Isotope Laboratories Inc.USA生產(chǎn)；IMark型全自動(dòng)酶標(biāo)儀（BIO-RAD，日本）。

一口鐘購于河北安國藥材批發(fā)市場，產(chǎn)地為云南省，經(jīng)天津醫(yī)科大學(xué)藥學(xué)院唐生安副教授鑒定為桉樹植物藍(lán)桉Eucalyptus globulusLabill.的干燥成熟果實(shí)，標(biāo)本（編號D20151011）現(xiàn)存放于天津醫(yī)科大學(xué)藥學(xué)院天然藥化實(shí)驗(yàn)室。

2 提取與分離

將一口鐘藥材（干質(zhì)量20 kg）粉碎，95%乙醇浸漬，每次浸漬3 d，一共浸漬5次，將浸漬液合并后減壓濃縮，得到乙醇提取物的浸膏（2992 g）。將乙醇提取物用水混懸，依次用石油醚、醋酸乙酯萃取3次，分別得到石油醚萃取物（1592 g）、醋酸乙酯萃取物（406 g）。

取石油醚萃取物800 g，經(jīng)硅膠柱色譜初步分離，石油醚：醋酸乙酯（60∶1→1∶1）梯度洗脫，得到16個(gè)組分Fr.1～16。Fr.6分別用石油醚-醋酸乙酯（30∶1、15∶1、8∶1、4∶1、2∶1）進(jìn)行梯度洗脫分離得到14個(gè)亞組分Fr.6.1～6.14。Fr.6.3（11 g）通過ODS柱色譜分離，甲醇-水（80∶20、90∶10、95∶5、98∶2）梯度洗脫，共得到16個(gè)亞組分Fr.6.3.1～6.3.16。Fr.6.3.1（187.6 mg）經(jīng)半制備HPLC（ODS-A，甲醇-水88∶12，0.3%醋酸，5 mL/min）分離，純化得到化合物1（13.3 mg，tR＝39.1 min）；Fr.6.3.9（672.9 mg）經(jīng)半制備HPLC（ODS-A，甲醇-水88∶12，0.3%醋酸，5 ml/min）分離，純化得到化合物12（76.9 mg，tR＝182.0 min）和3（26.3 mg，tR＝194.2 min）；Fr.6.3.11（105.9 mg）過半制備液相色譜柱（ODS-A，甲醇-水93∶7，0.3%醋酸，5 mL/min），純化得到化合物9（20.2 mg，tR＝263.9 min）、10（73.0 mg，tR＝204.0 min）。將Fr.6.8.2（517.9 mg）過半制備液相色譜柱（ODS-A，甲醇-水90∶10，0.3%醋酸），純化得到化合物11（13.1 mg，tR＝60.5 min）。Fr.6.8（7 g）進(jìn)行硅膠柱分離（二氯甲烷-甲醇-醋酸1000∶5∶3），得到17個(gè)亞組分Fr.6.8.1～6.8.17，將組分Fr.6.8.6與Fr.6.8.7合并，過半制備HPLC（ODS-A，甲醇-水89∶11，0.3%醋酸，5 mL/min）分離，得到化合物6（7.9 mg，tR＝49.7 min）和8（8.2 mg，tR＝46.7 min）。Fr.6.9（1 g）過正相硅膠柱（二氯甲烷-甲醇4∶1，0.3% 醋酸）得到化合物2（94.5 mg）。

Fr.14（59 g）組分，進(jìn)行硅膠柱分離 [二氯甲烷-甲醇-乙酸（80∶1∶1）]，得到14個(gè)亞組分Fr.14.1～14.14。Fr.14.4（26 g）過正相硅膠柱色譜[二氯甲烷-甲醇（10∶1）]分離，得到19個(gè)亞組分Fr.14.4.1～14.4.19，組分Fr.14.4.2（140.6 mg）通過半制備HPLC [ODS-A，甲醇-水（88∶12），0.3% 醋酸，5 mL/min]分離，得到化合物5（4.8 mg，tR＝118.3 min）。Fr.14.5與Fr.14.6合并，經(jīng)硅膠柱色譜分離，石油醚-醋酸乙酯（100∶1→1∶1）梯度洗脫得到19個(gè)亞組分Fr.14.6.1～14.6.19，F(xiàn)r.14.6.8和Fr.14.6.19分別用半制備HPLC純化 [ODS-A，甲醇-水（86∶14），0.5%醋酸，5 mL/min]，依次得到化合物4（35.8 mg）、13（264.3 mg）。

Fr.15經(jīng)Toyopearl HW-40凝膠柱色譜 [二氯甲烷-甲醇（2∶1）]分離，得到6個(gè)亞組分Fr.15.1～15.6，其中Fr.15.1經(jīng)硅膠柱色譜，以石油醚-二氯甲烷-醋酸乙酯-醋酸（40∶30∶1∶1）作為流動(dòng)相進(jìn)行分離，得到化合物14（27.5 mg）、15（17.4 mg）。

3 結(jié)構(gòu)鑒定

化合物1：黃色粉末。ESI-MSm/z: 255 [M＋H]+，分子式為C15H10O4。1H-NMR (400 MHz,pyridine-d5)δ: 12.11 (1H,s,H-8),12.01 (1H,s,1-OH),7.82 (1H,d,J= 7.2 Hz,H-5),7.67 (1H,m,H-6),7.29 (1H,d,J= 8.4 Hz,H-7),7.10 (1H,s,2-OH),2.47 (3H,s,H-CH3)；13C-NMR (100 MHz,pyridine-d5)δ: 162.7 (C-1),119.9 (C-2),149.4 (C-3),121.4 (C-4),124.6 (C-5),133.3 (C-6),124.4 (C-7),162.5 (C-8),192.6 (C-9),182.0 (C-10),137.0 (C-4a),115.9 (C-8a),113.8 (C-9a),133.7 (C-10a),22.3 (C-CH3)。上述波譜數(shù)據(jù)與文獻(xiàn)值基本一致[8]，故鑒定化合物1為大黃酚。

化合物2：淺黃色粉末。ESI-MSm/z: 487 [M＋H]+，分子式為C29H42O6。1H-NMR (400 MHz,pyridine-d5)δ: 10.54 (1H,s,8′-CHO),10.51 (1H,s,7′-CHO),3.74 (1H,dd,J= 12.8,4.4 Hz,H-9′),3.20 (3H,s,H-OCH3),2.59 (1H,dd,J= 12.8,4.0 Hz,H-10′a),2.29 (1H,dd,J= 10.0,4.4 Hz,H-1),1.25 (3H,s,H-14),1.19 (3H,overlapped,H-12),1.19 (3H,overlapped,H-13),0.99 (3H,d,J= 6.8 Hz,H-13′),0.94 (3H,overlapped,H-15),0.94 (3H,overlapped,H-12′)；13C-NMR (100 MHz,pyridine-d5)δ: 50.3 (C-1),24.4 (C-2),35.7 (C-3),48.7 (C-4),43.9 (C-5),27.9 (C-6),26.1 (C-7),20.4 (C-8),37.6 (C-9),79.6 (C-10),19.9 (C-11),29.1 (C-12),17.8 (C-13),18.6 (C-14),21.5 (C-15),171.4 (C-1′),106.6 (C-2′),171.3 (C-3′),106.6 (C-4′),170.6 (C-5′),108.6 (C-6′),192.3 (C-7′),192.0 (C-8′),35.6 (C-9′),34.6 (C-10′),27.9 (C-11′),24.8 (C-12′),22.4 (C-13′),47.9 (C-OCH3)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[9]，故鑒定化合物2為eucarobustol E。

化合物3：無定形粉末。ESI-MSm/z: 453 [MH]-，確定其分子式為C28H38O5。1H-NMR (400 MHz,pyridine-d5)δ: 10.55 (1H,s,8′-CHO),10.54 (1H,s,7′-CHO),5.22 (1H,s,H-2),3.58 (1H,dd,J= 11.6,3.6 Hz,H-9′),2.45 (1H,d,J= 10.0 Hz,H-10′a),1.48 (1H,d,J= 4.0 Hz,H-2),1.44 (1H,d,J= 3.2 Hz,H-10′b),1.42 (3H,s,H-15),1.20 (3H,overlapped,H-12),1.20 (3H,overlapped,H-13),1.05 (3H,overlapped,H-14),1.05 (3H,overlapped,H-12′),1.00 (3H,d,J= 6.6 Hz,H-13′)；13C-NMR (100 MHz,pyridine-d5)δ: 155.1 (C-1),121.7 (C-2),43.2 (C-3),52.7 (C-4),53.8 (C-5),30.3 (C-6),30.7 (C-7),26.3 (C-8),39.4 (C-9),39.6 (C-10),22.3 (C-11),30.2 (C-12),18.2 (C-13),21.9 (C-14),24.0 (C-15),175.4 (C-1′),109.4 (C-2′),174.9 (C-3′),109.1 (C-4′),173.6 (C-5′),109.1 (C-6′),194.0 (C-7′),193.7 (C-8′),43.5 (C-9′),38.7 (C-10′),30.0 (C-11′),25.2 (C-12′),23.4 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[9]，故鑒定化合物3為eucarobustol G。

化合物4：淺黃色固體。ESI-MSm/z: [M＋H]+469，分子式為C28H36O6。1H-NMR (400 MHz,pyridine-d5)δ: 10.28 (1H,s,CHO-7′),10.08 (1H,s,CHO-8′),5.02 (1H,s,H-14b),5.00 (1H,s,H-14a),4.83 (1H,s,H-12b),4.80 (1H,s,H-12a),4.25 (1H,d,J= 11.4 Hz,H-5),3.52 (1H,br d,J= 12.2 Hz,H-7),2.82 (1H,m,H-9a),2.81 (1H,dd,J= 12.1,2.0 Hz,H-6),2.55 (1H,dd,J= 6.8,2.0 Hz,H-9′),2.39 (1H,m,H-2b),2.27 (1H,brd,J= 13.3 Hz,H-9b),2.10 (1H,m,H-2a),1.98 (1H,m,H-8a),1.91 (1H,m,H-3b),1.85 (3H,s,H-13),1.73 (1H,m,H-11′),1.68 (1H,m,H-8b),1.49 (1H,m,H-10′b),1.29 (1H,m,H-3a),1.21 (1H,m,H-10′a),1.09 (3H,d,J= 6.8 Hz,H-13′),1.00 (3H,s,H-15),0.97 (3H,d,J= 6.9 Hz,H-12′)；13C-NMR (100 MHz,pyridine-d5)δ: 73.1 (C-1),33.3 (C-2),30.5 (C-3),36.5 (C-4),76.2 (C-5),46.3 (C-6),41.0 (C-7),24.7 (C-8),33.1 (C-9),148.1 (C-10),149.0 (C-11),107.7 (C-12),23.9 (C-13),110.2 (C-14),20.1 (C-15),169.2 (C-1′),104.4 (C-2′),168.0 (C-3′),104.5(C-4′),163.1 (C-5′),108.0 (C-6′),191.9 (C-7′),195.5 (C-8′),38.4 (C-9′),43.6 (C-10′),29.1 (C-11′),22.9 (C-12′),21.4 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[10]，故鑒定化合物4為 eucalyptal A。

化合物5：黃色粉末。ESI-MSm/z: 469 [M＋H]+，確定其分子式為C28H36O6。1H-NMR (400 MHz,pyridine-d5)δ: 10.32 (1H,s,7′-CHO),9.92 (1H,s,8′-CHO),5.12 (1H,s,H-14b),5.10 (1H,s,H-14a),4.27 (1H,d,J= 11.6 Hz,H-5),3.56 (1H,d,J= 11.6 Hz,H-6),2.97 (1H,ddd,J= 13.6,13.6,4.7 Hz,H-9b),2.86 (1H,dd,J= 13.6,4.2 Hz,H-8a),2.72 (1H,dd,J= 7.5,2.9 Hz,H-9′),2.48 (2H,ddd,J= 14.0,3.1,3.1 Hz,H-2b),2.34 (1H,m,H-9a),2.31 (1H,m,H-8b),2.20 (2H,ddd,J= 14.0,14.0,3.1 Hz,H-2a),2.20 (2H,ddd,J= 14.0,13.1,3.1 Hz,H-3b),1.84 (3H,s,H-13),1.78 (3H,s,H-12),1.29 (1H,m,H-10′a),1.60 (1H,m,H-10′b),1.50 (2H,ddd,J= 13.3,3.1,3.1 Hz,H-3a),1.16 (3H,d,J= 6.4,H-13′),1.11 (3H,s,H-15),0.91 (3H,d,J= 6.4,H-12′)；13C-NMR (100 MHz,pyridine-d5)δ: 73.9 (C-1),33.0 (C-2),30.5 (C-3),36.0 (C-4),75.8 (C-5),48.5 (C-6),128.0 (C-7),26.4 (C-8),33.2 (C-9),149.6 (C-10),127.0 (C-11),20.9 (C-12),20.7 (C-13),109.3 (C-14),19.6 (C-15),169.3 (C-1′),104.5 (C-2′),168.0 (C-3′),104.5 (C-4′),163.1 (C-5′),108.0 (C-6′),191.9 (C-7′),192.3 (C-8′),38.4 (C-9′),43.3 (C-10′),28.9 (C-11′),23.9 (C-12′),22.6 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[10]，故鑒定化合物5為eucalyptal C。

化合物6：無定形粉末。ESI-MSm/z: 401 [MH]-，確定其分子式為C23H30O6。1H-NMR (400 MHz,pyridine-d5)δ: 10.17 (1H,m,CHO-9),10.05 (1H,m,CHO-8),5.87 (1H,d,J= 10.0 Hz,H-2′),5.66 (1H,d,J= 10.0 Hz,H-3′),2.83 (1H,dd,J= 10.0,4.0 Hz,H-7),2.22 (1H,s,H-6′),1.90 (1H,dd,J= 13.6,2.8 Hz,H-5′a),1.79 (1H,overlapped,H-11),1.79 (1H,overlapped,H-8′),1.73 (1H,dd,J= 13.6,4.4 Hz,H-10a),1.70 (1H,m,H-10b),1.54 (3H,s,H-7′),1.51 (3H,d,J= 6.4 Hz,H-10′),1.50 (1H,m,H-5′b),0.99 (3H,d,J= 5.2 Hz,H-12),0.98 (3H,d,J= 6.0 Hz,H-13),0.94 (3H,m,H-9′)；13C-NMR (100 MHz,pyridine-d5)δ: 104.8 (C-1),161.9 (C-2),104.2 (C-3),168.0 (C-4),104.3 (C-5),169.5 (C-6),35.6 (C-7),192.2 (C-8),191.8 (C-9),43.9 (C-10),26.4 (C-11),23.5 (C-12),21.6 (C-13),77.3 (C-1′),137.3 (C-2′),131.4 (C-3′),73.0 (C-4′),38.5 (C-5′),38.1 (C-6′),27.9 (C-7′),36.7 (C-8′),16.8 (C-9′),17.1 (C-10′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[11]，故鑒定化合物6為eucalyptin C。

化合物7：無定形粉末。ESI-MSm/z: 401 [MH]-，確定其分子式為C23H30O6。1H-NMR (400 MHz,CDCl3)δ: 10.14 (1H,s,9-CHO),10.01 (1H,s,CHO-8),5.91 (1H,m,H-2′),5.81 (1H,m,H-3′),3.17 (1H,m,H-7),2.50 (1H,m,H-10a),2.09 (1H,m,H-6′),2.03 (1H,dd,J= 12.6,2.8 Hz,H-5′a),1.82 (1H,m,H-8′),1.67 (1H,m,H-11),1.40 (1H,m,H-10b),1.39 (3H,s,H-7′),1.32 (1H,m,H-5′b),1.02 (3H,d,J= 6.4 Hz,H-12),1.00 (3H,s,H-13),1.00 (3H,s,H-10′),0.99 (3H,d,J= 7.0 Hz,H-9′)；13C-NMR (100 MHz,CDCl3)δ: 103.2 (C-1),163.5 (C-2),104.3 (C-3),168.0 (C-4),104.3 (C-5),170.8 (C-6),29.1 (C-7),192.4 (C-8),191.9 (C-9),36.2 (C-10),25.2 (C-11),24.0 (C-12),21.0 (C-13),77.0 (C-1′),137.9 (C-2′),130.7 (C-3′),73.6 (C-4′),30.7 (C-5′),36.2 (C-6′),24.2 (C-7′),35.0 (C-8′),16.4 (C-9′),16.8 (C-10′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[11]，故鑒定化合物7為 eucalyptin D。

化合物8：淺黃色固體。ESI-MSm/z: 487 [M＋H]+，確定其分子式為C29H42O6。1H-NMR (400 MHz,pyridine-d5)δ: 10.56 (1H,s,7′-CHO),10.51 (1H,s,8′-CHO),3.62 (1H,m,H-9′),3.18 (3H,s,H-OCH3),2.74 (1H,brt,J= 12.0 Hz,H-10′a),2.33 (1H,overlapped,H-1),1.57 (1H,overlapped,H-10′b),1.36 (3H,s,H-15),1.23 (3H,s,H-12),1.18 (3H,s,H-14),1.14 (3H,s,H-13),1.03 (3H,s,H-12′),1.02 (3H,s,H-13′)；13C-NMR (100 MHz,pyridine-d5)δ: 53.9 (C-1),24.8 (C-2),40.7 (C-3),50.3 (C-4),49.5 (C-5),30.1 (C-6),26.7 (C-7),20.9 (C-8),38.0 (C-9),80.0 (C-10),19.9 (C-11),17.7 (C-12),29.5(C-13),19.0 (C-14),18.5 (C-15),171.2(C-1′),106.7 (C-2′),171.4(C-3′),106.8(C-4′),171.4(C-5′),108.8(C-6′),192.0(C-7′),192.2 (C-8′),41.6 (C-9′),36.4 (C-10′),27.9 (C-11′),22.2 (C-12′),25.4 (C-13′),48.5 (C-OCH3)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[11]，故鑒定化合物8為eucalyptin E。

化合物9：無定形粉末。ESI-MSm/z: 453 [MH]-，確定其分子式為C28H38O5。1H-NMR (400 MHz,pyridine-d5)δ: 10.55 (1H,s,H-13′),5.46 (1H,s,H-3),3.22 (1H,d,J= 1.6 Hz,H-8′a),3.20 (1H,d,J= 1.6 Hz,H-8′b),3.02 (1H,dd,J= 13.2,3.2 Hz,H-12′a),2.79 (1H,dd,J= 13.2,10.8 Hz,H-12′b),2.42 (1H,m,H-9′),1.88 (1H,m,H-8a),1.82 (1H,m,H-9a),1.69 (3H,s,H-15),1.46 (1H,m,H-8b),1.07 (1H,d,J= 3.6 Hz,H-9b),1.03 (3H,overlapped,H-10′),1.01 (3H,d,J= 2.0 Hz,H-12),1.00 (3H,overlapped,H-11′),0.93 (3H,s,H-13),0.87 (3H,s,H-14),0.54 (1H,m,H-7),0.46 (1H,m,H-6)；13C-NMR (100 MHz,pyridine-d5)δ: 43.9 (C-1),29.3 (C-2),121.5 (C-3),135.5 (C-4),44.6 (C-5),24.0 (C-6),19.8 (C-7),16.2 (C-8),34.5 (C-9),35.5 (C-10),18.5 (C-11),28.9 (C-12),16.1 (C-13),13.0 (C-14),21.7 (C-15),170.5 (C-1′),107.9(C-2′),173.0 (C-3′),106.9 (C-4′),167.6 (C-5′),105.8 (C-6′),206.8 (C-7′),23.1 (C-8′),25.8 (C-9′),23.4 (C-10′),23.4 (C-11′),23.1 (C-12′),193.2 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)值基本一致[12]，故鑒定化合物9為eucalrobusone A。

化合物10：白色粉末。ESI-MSm/z: 453 [MH]-，確定其分子式為C28H38O5。1H-NMR (400 MHz,pyridine-d5)δ: 10.52 (1H,s,CHO-13′),5.36 (1H,d,J= 4.4 Hz,H-6),4.89 (1H,s,H-12b),4.84 (1H,s,H-12a),3.15 (2H,d,J= 6.4 Hz,H-8′),3.03 (1H,dd,J= 13.2,2.0 Hz,H-12′a),2.79 (1H,dd,J= 13.2,10.8 Hz,H-12′b),2.48 (1H,m,H-4),2.40 (1H,m,H-9′),1.88 (1H,overlapped,H-9),1.85 (1H,overlapped,H-2),1.81 (1H,overlapped,H-1),1.74 (3H,s,H-13),1.65 (1H,m,H-8),1.54 (1H,m,H-3),1.16 (3H,s,H-15),1.13 (3H,s,H-14),1.00 (3H,s,H-11′),0.98 (3H,s,H-10′)；13C-NMR (100 MHz,pyridine-d5)δ: 49.8 (C-1),23.4 (C-2),34.0 (C-3),40.0 (C-4),149.8 (C-5),124.2 (C-6),42.3 (C-7),23.3 (C-8),34.9 (C-9),39.1 (C-10),148.8 (C-11),112.4 (C-12),22.7 (C-13),22.1 (C-14),23.0 (C-15),170.1 (C-1′),108.5 (C-2′),172.8 (C-3′),106.8 (C-4′),167.4 (C-5′),105.6 (C-6′),206.8 (C-7′),53.4 (C-8′),25.7 (C-9′),23.4 (C-10′),23.4 (C-11′),23.6 (C-12′),193.2 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[12]，故鑒定化合物10為eucalrobusone C。

化合物11：白色粉末。ESI-MSm/z: [M－H]-383，確定其分子式為C23H28O5。1H-NMR (400 MHz,pyridine-d5)δ: 10.54 (1H,s,13′-CHO),7.21 (1H,d,J= 12.0 Hz,H-2),7.05 (1H,d,J= 7.6 Hz,H-5),7.00 (1H,dd,J= 7.6,1.2 Hz,H-4),4.13 (2H,s,H-12),3.14 (1H,d,J= 6.4 Hz ,H-8′),2.71 (1H,m,H-7),2.38 (1H,m,H-9′),2.19 (3H,s,H-10),1.08 (3H,s,H-8),1.07 (3H,s,H-9),1.00 (3H,s,H-10′),0.99 (3H,s,H-11′)；13C-NMR (100 MHz,pyridine-d5)δ: 138.9 (C-1),126.1 (C-2),147.2 (C-3),124.1 (C-4),130.7 (C-5),134.5 (C-6),34.5 (C-7),24.7 (C-8),24.7 (C-9),19.6 (C-10),171.0 (C-1′),106.0 (C-2′),173.1 (C-3′),106.0 (C-4′),168.5 (C-5′),105.2 (C-6′),206.7 (C-7′),53.2 (C-8′),25.8 (C-9′),23.4 (C-10′),23.4 (C-11′),26.7 (C-12′),193.4 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[12]，故鑒定化合物11為 eucalrobusone F。

化合物12：白色粉末。ESI-MSm/z: [M－H]-467，確定其分子式為C28H36O6。1H-NMR (400 MHz,pyridine-d5)δ: 10.33 (1H,s,CHO-13′),10.30 (1H,s,CHO-12′),4.73 (1H,d,J= 4.0 Hz,H-2),3.50 (1H,d,J= 11.2 Hz,H-7′),2.34 (2H,m,H-3),1.95 (1H,d,J= 11.2 Hz,H-5),1.31 (3H,s,H-15),1.27 (3H,s,H-14),1.03 (3H,s,H-12),1.00 (3H,s,H-13),0.98 (3H,d,J= 6.2 Hz,H-10′),0.87 (3H,d,J= 6.0 Hz,H-11′),0.56 (1H,m,H-6),0.47 (1H,m,H-7)；13C-NMR (100 MHz,pyridine-d5)δ: 75.8 (C-1),91.3 (C-2),39.9 (C-3),44.5 (C-4),47.4 (C-5),23.5 (C-6),26.1 (C-7),22.1 (C-8),32.4 (C-9),64.1 (C-10),20.7 (C-11),29.0 (C-12),16.4 (C-13),23.5 (C-14),23.9 (C-15),173.8 (C-1′),116.1 (C-2′),170.8 (C-3′),107.8 (C-4′),170.8 (C-5′),105.9 (C-6′),44.6 (C-7′),42.4 (C-8′),26.8 (C-9′),21.8 (C-10′),25.1 (C-11′),194.5 (C-12′),193.0 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[13]，故鑒定化合物12為 eucalrobusone U。

化合物13：無色粉末。ESI-MSm/z: 487 [M＋H]+，分子式為C28H38O7。1H-NMR (400 MHz,pyridine-d5)δ: 10.50 (1H,s,CHO-8′),10.48 (1H,s,CHO-7′),3.51 (H,dd,J= 11.8,4.0 Hz,H-9′),2.71 (1H,dd,J= 13.4,4.0 Hz,H-10′a),2.68 (1H,m,H-9b),2.65 (1H,m,H-2b),2.54 (1H,dd,J= 9.3,7.0 Hz,H-9a),2.50 (1H,d,J= 7.0 Hz,H-5),2.37 (1H,m,H-2a),2.30 (1H,m,H-8a),2.17 (1H,m,H-3b),2.05 (3H,s,H-14),1.78 (1H,dd,J= 9.3,7.0 Hz,H-8b),1.75 (1H,dd,J= 10.4,3.5 Hz,H-3a),1.55 (1H,m,H-11′),1.40 (1H,dd,J= 13.4,4.1 Hz,H-10′b),1.34 (3H,s,H-15),1.13 (3H,s,H-12),1.11 (3H,s,H-13),0.89 (3H,d,J= 6.6 Hz,H-13′),0.86 (3H,d,J= 6.5 Hz,H-12′),0.58 (1H,d,J= 7.2 Hz,H-7)；13C-NMR (100 MHz,pyridine-d5)δ: 221.0 (C-1),36.4 (C-2),32.9 (C-3),48.1 (C-4),21.2 (C-5),27.9 (C-6),25.2 (C-7),44.9 (C-8),55.3 (C-9),208.3 (C-10),18.3 (C-11),16.6 (C-12),29.4 (C-13),29.6 (C-14),22.1 (C-15),173.1 (C-1′),107.7 (C-2′),174.1 (C-3′),107.6 (C-4′),173.1 (C-5′),105.9 (C-6′),192.3 (C-7′),192.4 (C-8′),40.2 (C-9′),36.8 (C-10′),27.9 (C-11′),20.2 (C-12′),24.9 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[14]，故鑒定化合物13為eucalyptone。

化合物14：無色油狀物。ESI-MSm/z: 387 [M＋H]+，分子式為C23H30O5。1H-NMR (400 MHz,CDCl3)δ: 9.93 (1H,s,CHO-8′),9.89 (1H,s,CHO-7′),5.79 (1H,dd,J= 10.1,4.1 Hz,H-1),5.45 (1H,dd,J= 9.8,1.9 Hz,H-6),2.70 (1H,m,H-9′),2.00 (1H,m,H-2),1.52 (3H,s,H-10)；13C-NMR (100 MHz,CDCl3)δ: 134.1 (C-1),38.6 (C-2),30.1 (C-3),38.0 (C-4),77.1 (C-5),129.1 (C-6),30.9 (C-7),20.0 (C-8),19.9 (C-9),27.5 (C-10),106.1 (C-1′),168.7 (C-2′),103.6 (C-3′),166.2 (C-4′),103.6 (C-5′),161.4 (C-6′),190.3 (C-7′),191.0 (C-8′),28.3 (C-9′),43.9 (C-10′),25.2 (C-11′),22.9 (C-12′),20.4 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道基本一致[15]，故鑒定化合物14為euglobal-Ia1。

化合物15：無色油狀物。ESI-MSm/z: 387 [M＋H]+，分子式為C23H30O5。1H-NMR (400 MHz,CDCl3)δ: 10.17 (1H,s,8′-CHO),10.06 (1H,s,7′-CHO),5.96 (1H,dd,J= 10.0,3.5 Hz,H-1),5.83 (1H,dd,J= 10.0,1.5 Hz,H-6),3.17 (1H,m,H-9′),2.04 (1H,m,H-2),1.80 (1H,m,H-10′b),1.57 (1H,dd,J= 9.4,11.4 Hz,H-10′a),1.40 (3H,s,H-10)；13C-NMR (100 MHz,CDCl3)δ: 134.3 (C-1),40.7 (C-2),22.4 (C-3),35.9 (C-4),78.0 (C-5),130.5 (C-6),31.9 (C-7),20.9 (C-8),20.6 (C-9),25.7 (C-10),104.9 (C-1′),169.8 (C-2′),103.9 (C-3′),167.8 (C-4′),104.4 (C-5′),163.3 (C-6′),191.4 (C-7′),192.1 (C-8′),29.7 (C-9′),36.8 (C-10′),25.3 (C-11′),23.5 (C-12′),21.8 (C-13′)。上述波譜數(shù)據(jù)與文獻(xiàn)報(bào)道一致[16]，故化合物15鑒定為euglobal-Ia2。

4 細(xì)胞毒活性研究

采用MTT法[17]測定細(xì)胞毒活性。將培養(yǎng)好的第6代的MCF-7細(xì)胞以5×104個(gè)/孔的密度接種于96孔板，每孔200 μL，置于培養(yǎng)箱中過夜。然后3孔為1組，加入終濃度為20 μmol/L的待測單體化合物，對照組加入等量含DMSO的培養(yǎng)基，同時(shí)設(shè)置順鉑為陽性對照組，37 ℃、5%CO2培養(yǎng)箱中培養(yǎng)24 h。取出96孔板，向孔內(nèi)加入提前放于室溫下解凍的MTT溶液（5 mg/mL，20 μL/孔），37 ℃培養(yǎng)4 h后，棄上清液，每孔加DMSO 150 μl，震蕩10 min后于1 h內(nèi)在酶聯(lián)免疫檢測儀上測其波長為490 nm的吸光度（A）值，重復(fù)測定3次，按照公式計(jì)算相應(yīng)的抑制率，見表1。

表1 部分化合物對MCF-7細(xì)胞增值的抑制作用Table 1 Inhibition rate of monomer compounds against MCF-7 cells

結(jié)果顯示，當(dāng)濃度為20 μmol/L時(shí)，化合物2～4、6、7、10～13和15的抑制作用高于陽性藥順鉑，表現(xiàn)出一定的抗腫瘤活性，其中化合物12的活性較好，抑制率達(dá)到80.53%，其IC50值為13.84 μmol/L。

利益沖突所有作者均聲明不存在利益沖突