期刊文献+
共找到4篇文章
< 1 >
每页显示 20 50 100
Enhanced absorption and inhibited metabolism of emodin by 2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucopyranoside: Possible mechanisms for Polygoni Multiflori Radix-induced liver injury 被引量:14
1
作者 YU Qiong JIANG Li-Long +4 位作者 LUO Na FAN Ya-Xi MA Jiang LI Ping LI Hui-Jun 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2017年第6期451-457,共7页
Polygoni Multiflori Radix(PMR) has been commonly used as a tonic in China for centuries. However, PMR-associated hepatotoxicity is becoming a safety issue. In our previous in vivo study, an interaction between stilben... Polygoni Multiflori Radix(PMR) has been commonly used as a tonic in China for centuries. However, PMR-associated hepatotoxicity is becoming a safety issue. In our previous in vivo study, an interaction between stilbenes and anthraquinones has been discovered and a hypothesis is proposed that the interaction between stilbene glucoside-enriching fraction and emodin may contribute to the side effects of PMR. To further support our previous in vivo results in rats, the present in vitro study was designed to evaluate the effects of 2, 3, 5, 4'-tetrahydroxystilbene-2-O-β-D-glucopyranoside(TSG) on the cellular absorption and human liver microsome metabolism of emodin. The obtained results indicated that the absorption of emodin in Caco-2 cells was enhanced and the metabolism of emodin in human liver microsomes was inhibited after TSG treatment. The effects of the transport inhibitors on the cellular emodin accumulation were also examined. Western blot assay suggested that the depressed metabolism of emodin could be attributed to the down-regulation of UDP-glucuronosyltransferases(UGTs) 1A8, 1A10, and 2B7. These findings definitively demonstrated the existence of interaction between TSG and emodin, which provide a basis for a better understanding of the underlying mechanism for PMR-induced liver injury. 展开更多
关键词 Polygoni Multiflori Radix HEPATOTOXICITY EMODIN 2 3 5 4-tetrahydroxystilbene-2-o-β-d-glucopyranoside Component interaction
原文传递
UPLC-Q-TOF-MS法分析枇杷叶的倍半萜苷类化合物 被引量:13
2
作者 赵磊 陈剑 +2 位作者 印敏 任冰如 李维林 《中成药》 CAS CSCD 北大核心 2015年第7期1498-1502,共5页
目的采用超高效液相-四级杆-飞行时间串联质谱(UPLC-Q-TOF-MS)技术对分离得到的枇杷叶总倍半萜苷类成分进行定性分析,并对其裂解途径进行研究总结。方法枇杷叶乙醇提取物经大孔树脂、聚酰胺柱色谱和RP-18柱色谱处理后,得到的枇杷叶总倍... 目的采用超高效液相-四级杆-飞行时间串联质谱(UPLC-Q-TOF-MS)技术对分离得到的枇杷叶总倍半萜苷类成分进行定性分析,并对其裂解途径进行研究总结。方法枇杷叶乙醇提取物经大孔树脂、聚酰胺柱色谱和RP-18柱色谱处理后,得到的枇杷叶总倍半萜苷采用Agilent ZORBAX SB-C18色谱柱(4.6 mm×100 mm,1.8μm),甲醇-0.1%甲酸水溶液为流动相进行梯度洗脱,ESI源负离子模式下采集质谱数据。结果从总倍半萜苷中得到5个倍半萜苷类化合物,其二级质谱裂解规律均相同,表现为逐个脱去寡糖链上的糖基,产生特征碎片离子m/z 675、529、383,最后生成m/z 205的特征苷元碎片。结论其中2个倍半萜苷类成分可能是仅在苷元C-6和C-7位上构型有差异的loquatifolin A和6,7-cis-nerolidol-3-O-α-L-rhamnopyranosyl-(1→4)-α-L-rhamnopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→6)]-β-D-glucopyranoside。 展开更多
关键词 枇杷叶 倍半萜苷 UPLC-Q-TOF-MS loquatifolin A 6 7-cis-nerolidol-3-o-α-L-rhamnopyranosyl-(1→4)-α-L-rh-amnopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside
下载PDF
龙胆泻肝汤中一个新的二氢查尔酮苷(英文) 被引量:1
3
作者 王芸 章漳 +2 位作者 杨莉 侴桂新 王峥涛 《中国天然药物》 SCIE CAS CSCD 2008年第4期259-261,共3页
目的:研究龙胆泻肝汤的化学成分。方法:硅胶柱,反向C18柱,Sephadex LH-20等色谱技术进行分离纯化'才艮据化合物的理化性质和光谱数据鉴定结构。结果:从龙胆泻肝汤中分离并鉴定了5个化合物,分别为:2′,4′-dihydroxydihydro cha... 目的:研究龙胆泻肝汤的化学成分。方法:硅胶柱,反向C18柱,Sephadex LH-20等色谱技术进行分离纯化'才艮据化合物的理化性质和光谱数据鉴定结构。结果:从龙胆泻肝汤中分离并鉴定了5个化合物,分别为:2′,4′-dihydroxydihydro chalcone-3′-C-β-glucopyranosyl-6′-D-β-D-glucopyranoside(1),异甘草苷元(2),剌甘草查尔酮(3),甘草查尔酮B(4),异甘草苷(5)。结论:化合物1为新化合物,化合物2~5为首次从龙胆泻肝汤中分离得到。 展开更多
关键词 龙胆泻肝汤 查尔酮 2 4′-dihydroxydihydrochalcone-3′-C-β-glucopyra-nosyl-6’-o-β-d-glucopyranoside
下载PDF
New flavan and unusual chalcone glycosides from Drypetes parvifolia 被引量:1
4
作者 Viviane Nadège Nenkep Jovita Chi Shirri +5 位作者 Hanh Trinh Van-Dufat Falindor Sipepnou Philippe Vérité Elisabeth Seguin Francois Tillequin Jean Wandji 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第8期943-946,共4页
Two new compounds 7-hydroxy-5-O-(β-D-glucopyranoside) flavan (1) and (Z)-4',6'-dihydroxy-2'-O-(β-D-glucopyranoside) chalcone (2), along with eight known compounds, were isolated from the stem bark of Dr... Two new compounds 7-hydroxy-5-O-(β-D-glucopyranoside) flavan (1) and (Z)-4',6'-dihydroxy-2'-O-(β-D-glucopyranoside) chalcone (2), along with eight known compounds, were isolated from the stem bark of Drypetes parvifolia (Euphorbiaceae). Their structures were established on the basis of spectroscopic analysis and chemical evidence. 展开更多
关键词 Drypetes parvifolia Flavonoid glycosides 7-Hydroxy-5-o-β-d-glucopyranoside flavan (Z)-4' 6'-Dihydroxy-2-o-(β-D-glucopyr-anoside) chalcone
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部