高等学校化学学报
高等學校化學學報
고등학교화학학보
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES
2015年
6期
1107-1111
,共5页
徐燕%田沙沙%俞和%杨文智%朱华结
徐燕%田沙沙%俞和%楊文智%硃華結
서연%전사사%유화%양문지%주화결
真菌%棘孢曲霉%核磁共振%黄酮%抗氧化活性
真菌%棘孢麯黴%覈磁共振%黃酮%抗氧化活性
진균%극포곡매%핵자공진%황동%항양화활성
Fungi%Aspergillus aculeatus%Nuclear magnetic resonance spectroscopy (NMR)%Flavanoid%Antioxidant activity
从土壤真菌棘孢曲霉( Aspergillus aculeatus)中分离得到2个新化合物和2个已知化合物,采用质谱(MS)、一维核磁共振波谱(1D NMR)、异核多键相关谱(HMBC)、异核单量子相关谱(HSQC)和旋转坐标NOE谱( ROESY)等方法对化合物的结构进行了鉴定,化合物2的顺反构型通过ROESY数据进一步确定。鉴定结果表明,2个新化合物分别为2-(2'-4'-6'-三羟基)-7-羟基-5-甲基色原酮{2-(2',4',6'-trihydroxyphenyl)-(7-hydroxy-5-methyl)chromone}(1)和(E)-4-羟基-3-[(3-甲基-4-羟基-2-丁烯)氧代]苯甲酸{(E)-4-hydroxy-3-[(4-hydroxy-3-methylbut-2-en-1-yl)oxy]benzoic acid}(2);2个已知化合物分别为(S)-2-[(2'-羟基)丙基]-5-甲基-7-羟基色原酮{2-(2'-hydroxypropyl)-5-methyl-7-hydroxychromone}(3)和(3R,4S)-8-羟基-3,4,5-三甲基-6酮-4,6-二氢-3H-异色烯-7-羧酸{(3R,4S)-8-hydroxy-3,4,5-trimethyl-6-oxo-4,6-dihydro-3H-isochromene-7-carbox-ylic acid}(4)。活性测试结果表明,这4个化合物均表现出一定的抗氧化活性。
從土壤真菌棘孢麯黴( Aspergillus aculeatus)中分離得到2箇新化閤物和2箇已知化閤物,採用質譜(MS)、一維覈磁共振波譜(1D NMR)、異覈多鍵相關譜(HMBC)、異覈單量子相關譜(HSQC)和鏇轉坐標NOE譜( ROESY)等方法對化閤物的結構進行瞭鑒定,化閤物2的順反構型通過ROESY數據進一步確定。鑒定結果錶明,2箇新化閤物分彆為2-(2'-4'-6'-三羥基)-7-羥基-5-甲基色原酮{2-(2',4',6'-trihydroxyphenyl)-(7-hydroxy-5-methyl)chromone}(1)和(E)-4-羥基-3-[(3-甲基-4-羥基-2-丁烯)氧代]苯甲痠{(E)-4-hydroxy-3-[(4-hydroxy-3-methylbut-2-en-1-yl)oxy]benzoic acid}(2);2箇已知化閤物分彆為(S)-2-[(2'-羥基)丙基]-5-甲基-7-羥基色原酮{2-(2'-hydroxypropyl)-5-methyl-7-hydroxychromone}(3)和(3R,4S)-8-羥基-3,4,5-三甲基-6酮-4,6-二氫-3H-異色烯-7-羧痠{(3R,4S)-8-hydroxy-3,4,5-trimethyl-6-oxo-4,6-dihydro-3H-isochromene-7-carbox-ylic acid}(4)。活性測試結果錶明,這4箇化閤物均錶現齣一定的抗氧化活性。
종토양진균극포곡매( Aspergillus aculeatus)중분리득도2개신화합물화2개이지화합물,채용질보(MS)、일유핵자공진파보(1D NMR)、이핵다건상관보(HMBC)、이핵단양자상관보(HSQC)화선전좌표NOE보( ROESY)등방법대화합물적결구진행료감정,화합물2적순반구형통과ROESY수거진일보학정。감정결과표명,2개신화합물분별위2-(2'-4'-6'-삼간기)-7-간기-5-갑기색원동{2-(2',4',6'-trihydroxyphenyl)-(7-hydroxy-5-methyl)chromone}(1)화(E)-4-간기-3-[(3-갑기-4-간기-2-정희)양대]분갑산{(E)-4-hydroxy-3-[(4-hydroxy-3-methylbut-2-en-1-yl)oxy]benzoic acid}(2);2개이지화합물분별위(S)-2-[(2'-간기)병기]-5-갑기-7-간기색원동{2-(2'-hydroxypropyl)-5-methyl-7-hydroxychromone}(3)화(3R,4S)-8-간기-3,4,5-삼갑기-6동-4,6-이경-3H-이색희-7-최산{(3R,4S)-8-hydroxy-3,4,5-trimethyl-6-oxo-4,6-dihydro-3H-isochromene-7-carbox-ylic acid}(4)。활성측시결과표명,저4개화합물균표현출일정적항양화활성。
In order to investigate new bioactive compounds, a piece of fungi Aspergillus aculeatus was obtained from the Jinyun mountain soil in Chongqing, China. By fermentation using Potato Dextrose( PD) within 14 d at 28 ℃, the extraction of ethyl acetate(103 g) was obtained. The extraction was then used for isolation of compounds through a series of study by classical separation methods, for example Octadecyl Silane( ODS) and Sephadex LH-20 . Two new compounds 2-( 2', 4', 6'-trihydroxy phenyl ) benzene-( 7-hydroxy-5-methyl ) chromone ( 1 ) and ( E )-4-hydroxy-3-[ ( 4-hydroxy-3-methylbut-2-en-1-yl ) oxy ] benzoic acid ( 2 ) were obtained. The structures were elucidated using mass spectrometry(MS), one demensional nuclear magnetic resonance spectroscopy ( 1 D NMR ) , heteronuclear multiple bond correlation ( HMQC ) , heteronuclear single quanturn correlation(HMBC) and rotating-frame overhauser effect spectroscopy(ROESY). Other two known compounds 2-(2'-hydroxypropyl)-5-methyl-7-hydroxychromone(3) and (3R, 4S)-8-hydroxy-3,4,5- trime-thyl-6-oxo-4,6-dihydro-3H-isochromene-7-carboxylic acid ( 4 ) were obtained. Compounds 2 to 4 exhibited some 2,2-diphenyl-1-picrylhydrazyl(DPPH) antioxidant activity.