西北药学杂志
西北藥學雜誌
서북약학잡지
2013年
6期
559-562
,共4页
高阳%孙凡森%苏娅萍%杨敏飞%姜会敏%李教社%张海龙
高暘%孫凡森%囌婭萍%楊敏飛%薑會敏%李教社%張海龍
고양%손범삼%소아평%양민비%강회민%리교사%장해룡
华山松%二萜%唐松酸%痛风%黄嘌呤氧化酶抑制剂
華山鬆%二萜%唐鬆痠%痛風%黃嘌呤氧化酶抑製劑
화산송%이첩%당송산%통풍%황표령양화매억제제
Pinus armandii%diterpenoids%lambertianic acid%gout%xanthine oxidase inhibitors
目的:研究华山松松节的化学成分和黄嘌呤氧化酶抑制活性。方法通过各种柱色谱方法分离化合物,通过理化性质和波谱数据进行结构鉴定,对提取物和分离得到的化合物通过紫外分光光度法测定黄嘌呤氧化酶抑制活性。结果从松节提取物的石油醚部分共分离得到8个化合物,分别鉴定为异海松-7-烯-18-酸(1),唐松酸(2),3β,21α-二甲氧基锯齿石松-14-烯(3),3β-甲氧基-21α-乙酰氧基-锯齿石松-14-烯(4),3-甲氧基-锯齿石松-14-烯-21-酮(5),β-谷甾醇(6),胆甾醇肉豆蔻酸酯(7)和山嵛酸(8)。结论化合物3为首次从该植物中分离得到,并首次报道了该化合物的碳谱数据;化合物1和2具有一定的黄嘌呤氧化酶抑制作用。
目的:研究華山鬆鬆節的化學成分和黃嘌呤氧化酶抑製活性。方法通過各種柱色譜方法分離化閤物,通過理化性質和波譜數據進行結構鑒定,對提取物和分離得到的化閤物通過紫外分光光度法測定黃嘌呤氧化酶抑製活性。結果從鬆節提取物的石油醚部分共分離得到8箇化閤物,分彆鑒定為異海鬆-7-烯-18-痠(1),唐鬆痠(2),3β,21α-二甲氧基鋸齒石鬆-14-烯(3),3β-甲氧基-21α-乙酰氧基-鋸齒石鬆-14-烯(4),3-甲氧基-鋸齒石鬆-14-烯-21-酮(5),β-穀甾醇(6),膽甾醇肉豆蔻痠酯(7)和山崳痠(8)。結論化閤物3為首次從該植物中分離得到,併首次報道瞭該化閤物的碳譜數據;化閤物1和2具有一定的黃嘌呤氧化酶抑製作用。
목적:연구화산송송절적화학성분화황표령양화매억제활성。방법통과각충주색보방법분리화합물,통과이화성질화파보수거진행결구감정,대제취물화분리득도적화합물통과자외분광광도법측정황표령양화매억제활성。결과종송절제취물적석유미부분공분리득도8개화합물,분별감정위이해송-7-희-18-산(1),당송산(2),3β,21α-이갑양기거치석송-14-희(3),3β-갑양기-21α-을선양기-거치석송-14-희(4),3-갑양기-거치석송-14-희-21-동(5),β-곡치순(6),담치순육두구산지(7)화산유산(8)。결론화합물3위수차종해식물중분리득도,병수차보도료해화합물적탄보수거;화합물1화2구유일정적황표령양화매억제작용。
Objective To study the chemical constituents of the knobs of Pinus armandii and their xanthine oxidase inhibitory ac-tivities .Methods Compounds were isolated and purified by using various chromatographic technologies and their structures were identified on the basis of physicochemical properties and spectroscopic data .The xanthine oxidase inhibitory activities were deter-mined by UV spectrophotometric method .Results Eight compounds were identified as isopimara-7-en-18-oic acid (1) ,lambertian-ic acid (2) ,3β,21α-dimethoxyserrat-14-ene (3) ,3β-methoxyl-21α-acetoxyserrat-14-ene (4) ,3β-methoxyserrat-14-en-21-one (5) ,β-sitosterol (6) ,cholesteryl myristate (7) and docosanoic acid (8) .Conclusions Compound 3 was isolated from this plant for the first time ,and also its 13C-NMR data were reported for the first time .Compound 1 and 2 showed some xanthine oxidase inhibitory activities .