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A New Iridoid Glycoside and a New Iridoid from Pedicularis kansuensis f. albiflora 被引量:4
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作者 Cheng Shan YUAN, Wei Dong XIE, Xiu Ping YANG, Zhong Jian JIADepartment of Chemistry, National Laboratory of Applied Organic Chemistry, Lanzhou University,Lanzhou 730000 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第9期932-933,共2页
A new iridoid glycoside 1 and a new iridoid 2 were isolated from the whole plant of Pedicularis kansuensis f. albiflora. Their structures were elucidated by spectroscopie methods.
关键词 Pedicularis kansuensis f. albiflora SCROPHULARIACEAE iridoid glycoside iridoid.
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巴戟天中环烯醚萜苷类成分的测定及提取工艺研究
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作者 揭小玲 周阿容 +5 位作者 詹清 林梦丹 郑孝贤 王海龙 陈秀明 方东升 《福建分析测试》 2026年第1期1-6,共6页
建立测定巴戟天中环烯醚萜苷类成分(水晶兰苷和去乙酰基车叶草苷酸)含量的HPLC法,并优化其超声辅助提取工艺。HPLC法色谱条件:检测波长为235 nm,色谱柱为月旭Ulimate AQ-C18柱(4.6 mm×250 mm,5μm),流动相为乙腈-0.1%甲酸溶液(5∶9... 建立测定巴戟天中环烯醚萜苷类成分(水晶兰苷和去乙酰基车叶草苷酸)含量的HPLC法,并优化其超声辅助提取工艺。HPLC法色谱条件:检测波长为235 nm,色谱柱为月旭Ulimate AQ-C18柱(4.6 mm×250 mm,5μm),流动相为乙腈-0.1%甲酸溶液(5∶95),流速为0.8 mL/min,柱温为30℃。方法学验证表明,水晶兰苷和去乙酰基车叶草苷酸分别在8.485~271.504μg/mL和2.279~72.943μg/mL范围内线性关系良好(R^(2)≥0.999),精密度、稳定性、重复性试验的RSD均小于2%,加样回收率符合规定要求。在提取工艺优化中,以水晶兰苷和去乙酰基车叶草苷酸两者总提取量为评价指标,通过单因素试验考察溶剂量、超声温度、超声时间对总提取量的影响,并采用三因素三水平正交试验进行优化。确定最佳工艺为:加入6倍量纯化水,10000 r/min匀浆2 min后,再于70℃超声提取50 min。在此条件下,总提取量达8.943 mg/g(以湿基计)。该优化工艺稳定可靠、操作简便且环境友好,为巴戟天中环烯醚萜苷类成分的提取及相关产品的深度开发提供技术支撑。 展开更多
关键词 巴戟天 环烯醚萜苷类 水晶兰苷 去乙酰基车叶草苷酸 HPLC 超声辅助提取
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A New Acylated Iridoid Glucoside from Avicennia marina 被引量:2
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作者 Yah FENG Xiao Ming LI +1 位作者 Xiao Juan DUAN Bin Gui WANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第9期1201-1204,共4页
A new acylated iridoid glucoside, namely, 2'-O-(5-phenyl-2E, 4E-pentadienoyl)- mussaenosidic acid, was isolated from the aerial parts of the mangrove plant Avicennia marina. The structure of the new compound was es... A new acylated iridoid glucoside, namely, 2'-O-(5-phenyl-2E, 4E-pentadienoyl)- mussaenosidic acid, was isolated from the aerial parts of the mangrove plant Avicennia marina. The structure of the new compound was established on the basis of various NMR spectroscopic analyses, including 2D NMR techniques (^1H-^1H COSY, HMQC, and HMBC) and HR-FAB-MS. This compound displayed moderate antioxidant activity. 展开更多
关键词 Avicennia marina 2'-O-(5-phenyl-2E 4E-pentadienoyl)-mussaenosidic acid iridoid.
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龙胆化学成分研究
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作者 陈佳琪 刘冠科 +4 位作者 叶繁庆 赵杨涛 姚铁 张冰洋 邱峰 《中国药物化学杂志》 2026年第1期40-48,共9页
目的对龙胆的化学成分进行研究,完善其物质基础。方法采用硅胶、ODS、Sephadex LH-20、MCI柱色谱以及半制备高效液相色谱等色谱分离技术,对龙胆的75%(体积分数)乙醇提取物进行分离,并利用核磁共振波谱、高分辨质谱等方法鉴定化合物的结... 目的对龙胆的化学成分进行研究,完善其物质基础。方法采用硅胶、ODS、Sephadex LH-20、MCI柱色谱以及半制备高效液相色谱等色谱分离技术,对龙胆的75%(体积分数)乙醇提取物进行分离,并利用核磁共振波谱、高分辨质谱等方法鉴定化合物的结构。结果从龙胆的75%(体积分数)乙醇提取物中分离鉴定出11个化合物,分别鉴定为(E)-甲基-4-羟基-3-(3-羰基-1-丁烯基)-苯甲酸(1)、甲基-4-羟基-3-(3′-甲基-2′-丁烯基)-苯甲酸(2)、5,6-dihydro-4-(1,3-dihydroxybutan-2-yl)-3-(hydroxymethyl)pyran-2-one(3)、獐牙菜内酯A(4)、旋叶内酯B(5)、(-)-獐牙菜苷元A(6)、3,4-dihydro-5-(1-hydroxyethyl)-1 H-pyrano[3,4-c]pyridin-1-one(7)、villoside(8)、2-(3′-O-β-D-吡喃葡萄糖基)苯甲酰氧基龙胆酸(9)、poacynose(10)、龙胆苷B(11)。结论化合物1为新化合物,化合物3~9、11为首次从该属植物中分离得到,化合物10为首次从龙胆中分离得到。 展开更多
关键词 龙胆 化学成分 环烯醚萜 生物碱 酚类
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杜仲中环烯醚萜类化合物的研究进展
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作者 张宝军 洪燕龙 +1 位作者 张磊 王健英 《中国新药杂志》 北大核心 2026年第1期46-54,共9页
杜仲作为我国传统补益类药材,具有悠久的用药历史和广阔的药食同源产品开发应用前景。杜仲中富含环烯醚萜类成分,因其结构多样性和药理多效性,近年来得到了广泛的关注和研究,目前共分离鉴定了杜仲环烯醚萜类化学成分59种,包含苷类40种... 杜仲作为我国传统补益类药材,具有悠久的用药历史和广阔的药食同源产品开发应用前景。杜仲中富含环烯醚萜类成分,因其结构多样性和药理多效性,近年来得到了广泛的关注和研究,目前共分离鉴定了杜仲环烯醚萜类化学成分59种,包含苷类40种、非苷类19种。现代药理研究表明,该类成分作为杜仲的主要活性成分之一,在神经保护、骨保护、护肾保肝、抗氧化、抗炎、抗肿瘤、镇痛、抗动脉粥样硬化、降血压等方面发挥着重要作用,但仍有大部分杜仲环烯醚萜类成分的药理作用尚未得到深入研究及系统阐述。本文对杜仲环烯醚萜类成分的结构、种类、药理作用进行归类总结,以期为进一步的药理作用及构效关系研究提供科学参考,为其新药及药食同源类产品的开发奠定理论基础。 展开更多
关键词 杜仲 环烯醚萜类 化学成分 药理作用
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翁源巴戟天总环烯醚萜的提取及抗氧化研究
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作者 张天华 黄紫红 +2 位作者 张旭杭 冯梓健 胡心蕊 《中国饲料》 北大核心 2026年第3期58-63,共6页
为提高韶关翁源巴戟天总环烯醚萜得率,本试验采用纤维素酶辅助超声法提取,通过单因素试验与Box-Behnken响应面法设计试验优化工艺,并对总环烯醚萜的体外抗氧化活性进行了研究。结果表明:酶辅助超声提取巴戟天总环烯醚萜的最佳工艺条件为... 为提高韶关翁源巴戟天总环烯醚萜得率,本试验采用纤维素酶辅助超声法提取,通过单因素试验与Box-Behnken响应面法设计试验优化工艺,并对总环烯醚萜的体外抗氧化活性进行了研究。结果表明:酶辅助超声提取巴戟天总环烯醚萜的最佳工艺条件为:酶量2%、酶解时间2 h、液料比33:1(mL/g)、超声时间46 min、乙醇浓度39%。此参数下,总环烯醚萜得率为30.86%,与预测值的相对误差为0.16%。此外,巴戟天总环烯醚萜提取物具有一定的抗氧化活性,对超氧阴离子自由基清除的IC50为5.582 mg/mL,同时对钼酸铵有良好的还原能力。 展开更多
关键词 巴戟天总环烯醚萜 提取工艺 响应面法 抗氧化活性
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基于尿液代谢组学和网络药理学探讨玄参大极性环烯醚萜防治阴虚火旺型甲亢的作用机制
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作者 卢旭 何佳馨 +4 位作者 李静 刘泽宸 李玲 叶涛 张宁 《药物评价研究》 北大核心 2026年第1期69-82,共14页
目的 基于代谢组学和网络药理学探讨玄参大极性环烯醚萜苷(HPISN)防治阴虚火旺型甲亢的潜在作用机制。方法雄性SD大鼠随机分为对照组、模型组、HPISN(205 mg·kg^(-1))组,每组10只,分别饲养于代谢笼中。除对照组外,采用优甲乐诱导... 目的 基于代谢组学和网络药理学探讨玄参大极性环烯醚萜苷(HPISN)防治阴虚火旺型甲亢的潜在作用机制。方法雄性SD大鼠随机分为对照组、模型组、HPISN(205 mg·kg^(-1))组,每组10只,分别饲养于代谢笼中。除对照组外,采用优甲乐诱导阴虚火旺甲亢模型,90 min后ig给药,每天1次,连续15 d;采用超高效液相色谱-飞行时间质谱(UPLC-TOFMS)技术对大鼠尿液进行代谢组学分析,筛选差异代谢物。基于文献研究筛选得到玄参大极性环烯醚萜苷类活性成分,利用网络药理学、分子对接技术预测玄参大极性环烯醚萜苷防治阴虚火旺甲亢的潜在作用机制。将代谢组学中获得的差异代谢物与网络药理学中获得的“HPISN-甲亢”交集靶点导入Cytoscape 3.9.1软件,并使用Metscape插件构建“化合物-反应-酶-基因”网络,以寻找基因和代谢物之间的重要关联。结果 与对照组相比,模型组中有13个差异代谢物显著下调(P<0.05),11个差异代谢物显著上调(P<0.05);与模型组相比,HPISN组大鼠上述指标水平均显著逆转(P<0.05)。网络药理学筛选出HPISN作用于甲亢的8个核心靶点,分别为ALB、INS、TP53、EGFR、CTNNB1、IL10、STAT3、ANXA5;核心活性成分有5个,分别为哈巴苷(harpagide)、二氢梓醇(dihydrocatalpol)、8-O-阿魏酰基哈巴苷(8-O-feruloylharpagide)、球花苦苷(globularin)、6-O-α-L-rhamnopyranosylaucubin;GO功能富集结果显示核心靶点影响的生物过程主要包括RNA聚合酶II启动子转录的正调控、信号转导、基因表达的正向调节等;KEGG富集分析结果表明,HPISN可能调控缺氧诱导因子1(HIF-1)等信号通路。代谢组学联合网络药理学分析发现关键靶点为琥珀酸脱氢酶复合体A亚基(SDHA)、柠檬酸合成酶(CS)。结论 HPISN防治阴虚火旺甲亢的机制可能与作用于SDHA、CS等靶点,干预HIF-1等信号通路,引起差异代谢物变化有关。 展开更多
关键词 玄参 大极性环烯醚萜苷 阴虚火旺型甲亢 尿液代谢组学 网络药理学 分子对接 缺氧诱导因子1(HIF-1) 琥珀酸脱氢酶复合体A亚基(SDHA) 柠檬酸合成酶(CS)
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Anti-inflammatory iridoids from the stems of Cistanche deserticola cultured in Tarim Desert 被引量:12
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作者 NAN Ze-Dong ZHAO Ming-Bo +4 位作者 Zeng Ke-Wu TIAN Shuai-Hua WANG Wei-Nan JIANG Yong TU Peng-Fei 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2016年第1期61-65,共5页
In order to determine the chemical constituents of Cistanche deserticola cultured in Tarim desert,a systematically phytochemical investigation was carried out.The constituents were isolated by silica gel,Sephadex LH-2... In order to determine the chemical constituents of Cistanche deserticola cultured in Tarim desert,a systematically phytochemical investigation was carried out.The constituents were isolated by silica gel,Sephadex LH-20,MCI gel,ODS column chromatography,and semi-preparative HPLC.Their structures were determined on the basis of MS and NMR spectroscopic analyses,by chemical methods,and/or comparison with literature data.The anti-inflammatory activities of the isolates were evaluated for their inhibitory effects on the lipopolysaccharide(LPS)-induced nitric oxide(NO)production in BV-2 mouse microglial cells.Nine iridoids were isolated and identified as cistadesertoside A(1),cistanin(2),cistachlorin(3),6-deoxycatalpol(4),gluroside(5),kankanoside A(6),ajugol(7),bartsioside(8),and 8-epi-loganic acid(9).Compound 9 exhibited potent inhibition on the NO production with an IC_(50) value being 5.2 μmol·L^(-1),comparable to the positive control quercetin(4.3 μmol·L^(-1)).Compound 1 was a new iridoid,and compounds 5,6,and 8 were isolated from this species for the first time. 展开更多
关键词 CISTANCHE deserticola iridoidS Structure ELUCIDATION Anti—inflammatory activity
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A new iridoid from Incarvillea delavayi 被引量:9
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作者 Tao Lu Wei Dong Zhang +3 位作者 Yue Hu Pei Chuan Zhang Jin Cheng Li YunHeng Shen 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第12期1512-1514,共3页
A new iridoid was isolated from the 80% ethanol extract of the whole plant of Incarvillea delavayi. Its structure was defined, and named incarvillic acid, on the basis of spectral evidences.
关键词 Incarvillea delavayi BIGNONIACEAE iridoid Incarvillic acid
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A new iridoid glycoside from Gardenia jasminoides 被引量:10
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作者 Xiao Qin Zhou Zhi Ming Bi +2 位作者 Ping Li Dan Tang Hal Xia Cai 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第10期1221-1223,共3页
A new iridoid glycoside, 6'-O-sinapoylgeniposide, was isolated from Gardeniajasminoides Ellis and its structure was elucidated on the basis of 1D and 2D NMR, HR-ESI-MS techniques.
关键词 Gardenia jasminoides iridoid glycoside 6'-O-Sinapoylgeniposide
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Two new epimeric pairs of iridoid from mangrove plant Scyphiphora hydrophyllacea 被引量:8
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作者 Yan Bo Zeng Wen Li Mei +3 位作者 You Xing Zhao Ling Zhuang Kui Hong Hao Fu Dai 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第12期1509-1511,共3页
Two new epimeric pairs of iridoid scyphiphin A1 (la), A2 (lb) and scyphiphin B 1 (2a), B2 (2b) were isolated from Scyphiphora hydrophyllacea Gaertn. F. Their structures were elucidated by spectroscopic methods... Two new epimeric pairs of iridoid scyphiphin A1 (la), A2 (lb) and scyphiphin B 1 (2a), B2 (2b) were isolated from Scyphiphora hydrophyllacea Gaertn. F. Their structures were elucidated by spectroscopic methods. The mixture of scyphiphin B 1 and scyphiphin B2 showed moderate cytotoxicity against human hepatoma SMMC-7721 cell line in vitro by MTT method. 展开更多
关键词 Scyphiphora hydrophyllacea Gaertn. E iridoid CYTOTOXICITY SMMC-7721
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Cornel iridoid glycoside induces autophagy to protect against tau oligomer neurotoxicity induced by activation of glycogen synthase kinase-3β 被引量:4
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作者 YANG Cui-cui LI Xue-lian +3 位作者 ZHANG Li LI Ya-li LI Lin ZHANG Lan 《中国药理学与毒理学杂志》 CAS 北大核心 2019年第6期456-456,共1页
Tau oligomers are the etiologic molecules of Alzheimer disease(AD), and correlate strongly with neuronal loss and exhibit neurotoxicity. Recent evidence indicates that small tau oligomers are the most relevant toxic a... Tau oligomers are the etiologic molecules of Alzheimer disease(AD), and correlate strongly with neuronal loss and exhibit neurotoxicity. Recent evidence indicates that small tau oligomers are the most relevant toxic aggregate species. The aim of the present study was to investigate the mechanisms of cornel iridoid glycoside(CIG) on tau oligomers and cognitive functions. We injected wortmannin and GF-109203 X(WM/GFX, 200 μmol·L-1 each) into the lateral ventricles to induce tau oligomer and memory impairment in rats. When oral y administered with CIG at 60 and 120 mg·kg-1 per day for 14 d, CIG decreased the escape latency in Morris water maze test. We also found that CIG restored the expression of presynaptic p-synapsin, synaptophysin, and postsynaptic density-95(PSD-95) decreased by WM/GFX in rat cortex. CIG reduced the accumulation of tau oligomers in the brain of WM/GFX rats and in cells transfected with wild type glycogen synthase kinase-3β(wt GSK-3β). In addition, CIG up-regulated the levels of ATG7, ATG12, Beclin-1, and LC3 II in vivo and in vitro, suggesting the restoration of autophagy function. These results suggest that CIG could ameliorate memory deficits and regulate memory-associated synaptic proteins through the clearance of tau oligomers accumulation. Moreover, CIG clears tau oligomers by restoring autophagy function. 展开更多
关键词 cornel iridoid GLYCOSIDE AUTOPHAGY TAU OLIGOMER GLYCOGEN synthase kinase-3β
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A new iridoid glycoside from Paederia scandens 被引量:5
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作者 He, Da Hai Chen, Jin Song +1 位作者 Wang, Xiao Ling Ding, Ke Yi 《Chinese Chemical Letters》 SCIE CAS CSCD 2010年第4期437-439,共3页
A new glycoside named 6β-O-β-D-glucosylpaederosidic acid(1) was isolated from Paederia scandens and its structure was elucidated on the basis of spectroscopic and chemical evidence,together with four known iridoids,... A new glycoside named 6β-O-β-D-glucosylpaederosidic acid(1) was isolated from Paederia scandens and its structure was elucidated on the basis of spectroscopic and chemical evidence,together with four known iridoids,paederoside(2),paederosidic acid(3),paederosidic acid methyl ester(4),and deacetyl asperulosidic acid methyl ester(5).Compound 5 was isolated from this plant for the first time. 展开更多
关键词 Paederia scandens iridoidS Chemical structure 6β-O-β-D-Glucosylpaederosidic acid Deacetyl asperulosidic acid methyl ester
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Two New Antibacterial Iridoids from Patrinia rupestris 被引量:4
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作者 Xiu Ping YANG Cheng Shan YUAN Zhong Jian JIA 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第3期337-340,共4页
Two new iridoids (1 and 2) were isolated from the roots of Patrinia rupestris (Pail.) Juss. Their structures were elucidated by spectroscopic methods. Compounds 1 and 2 exhibited strong antibacterial activities ag... Two new iridoids (1 and 2) were isolated from the roots of Patrinia rupestris (Pail.) Juss. Their structures were elucidated by spectroscopic methods. Compounds 1 and 2 exhibited strong antibacterial activities against Eschecichia coli and Staphylococcus aureus, respectively. 展开更多
关键词 Patrinia rupestris VALERIANACEAE iridoidS antibacterial activity.
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A New Secoiridoidal Glucoside from Gentiana rigescens(Gentianaceae) 被引量:16
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作者 XU Min WANG Dong +1 位作者 ZHANG Ying-Jun YAN Chong-Ren 《云南植物研究》 CSCD 北大核心 2006年第6期669-672,共4页
A new acylated secoiridoidal glucoside,named gentiorigenoside A(1),was isolated from the root of Centiarm rigescens(Gentianaceae),together with eight known compounds,gentiopicroside(2),6'-O-β-D-glucopyranosyl gen... A new acylated secoiridoidal glucoside,named gentiorigenoside A(1),was isolated from the root of Centiarm rigescens(Gentianaceae),together with eight known compounds,gentiopicroside(2),6'-O-β-D-glucopyranosyl gentiopicroside(3),loganic acid(4),6'-O-β-D-glucopyranosyl loganic acid(5),sweroside(6),2'-(o,m-dihydoxybenzyl)-sweroside(7),swertiamarin(8)and secologanoside(9).heir structures were elucidated on the basis of detailed spectroscopic analysis.Iridoidal glucosides 3,5 and 9 were isolated for the first time from the title plant. 展开更多
关键词 Centiana rigescens iridoidal glucosides Gentiorigenoside A
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Isoflavones’effects on pharmacokinetic profiles of main iridoids from Gardeniae Fructus in rats 被引量:4
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作者 Ruirui Chang Jialin Liu +5 位作者 Yusha Luo Taohong Huang Qiang Li Jun Wen Weidong Chen Tingting Zhou 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2020年第6期571-580,共10页
Gardeniae Fructus(GF)and Semen Sojae Praeparatum(SSP)are both medicine food homologies and widely used in Chinese clinical prescriptions together.The research investigated the pharmacokinetics of four iridoids in norm... Gardeniae Fructus(GF)and Semen Sojae Praeparatum(SSP)are both medicine food homologies and widely used in Chinese clinical prescriptions together.The research investigated the pharmacokinetics of four iridoids in normal rats and isolfavones-fed rats,which were administered with isolfavones from SSP for 7,14,21 and 28 consecutive days.A validated LC-MS/MS method was developed for determining shanzhiside,genipin-1-gentiobioside,geniposide and their metabolite genipin in rat plasma.Plasma samples were pretreated by solid-phase extraction using paeoniflorin as the internal standard.The chromatographic separation was performed on a Waters Atlantis T3(4.6 mm×150 mm,3 mm)column using a gradient mobile phase consisting of acetonitril and water(containing 0.06%acetic acid).The mass detection was under the multiple reaction monitoring(MRM)mode via polarity switching between negative and positive ionization modes.The calibration curves exhibited good linearity(r>0.997)for all components.The lower limit of quantitation was in the range of 1 e10 ng/m L.The intra-day and inter-day precisions(RSD)at three different levels were both less than 12.2%and the accuracies(RE)ranged fromà10.1%to 16.4%.The extraction recovery of them ranged from 53.8%to 99.7%.Pharmacokinetic results indicated the bioavailability of three iridoid glycosides and the metabolite,genipin in normal rats was higher than that in rats exposed to isoflavones.With the longer time of administration of isoflavones,plasma concentrations of iridoids decreased,while genipin sulfate,the phase II metabolite of genposide and genipin-1-gentiobioside,appeared the rising exposure.The pharmacokinetic profiles of main iridoids from GF were altered by isoflavones. 展开更多
关键词 iridoidS Gardeniae fructus ISOFLAVONES Rat PHARMACOKINETICS LC-MS/MS
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Iridoid Glycosides from Buddleja lindeyana 被引量:6
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作者 LUJiang-hai PUXiao-ping +1 位作者 TUGuang-zhong ZHAOYu-ying 《Journal of Chinese Pharmaceutical Sciences》 CAS 2004年第3期151-154,共4页
Aim To study the chemical constituents of Buddleja lindeyana. Methods The constituents were separated and purified by different methods of chromatography, and their structures were elucidated by IR, MS and NMR. Result... Aim To study the chemical constituents of Buddleja lindeyana. Methods The constituents were separated and purified by different methods of chromatography, and their structures were elucidated by IR, MS and NMR. Results Three iridoid glycosides and two other compounds were isolated from Buddleja lindeyana. Their structures were elucidated to be 6-O-feruloylajugol ( 1 ), erythro-6-oxo-4′-( 3-methoxyl-4-hydroxyphenylglycol-8')-feruloylaj-ugol ( 2 ), threo-6-oxo-4′-(3-methoxyl-4-hydroxyphenylglycol-8')-feruloylajugol ( 3 ), tetra-cosanoic acid 2,3-dihydroxypropyl ester (4), and galactitol (5). Conclusion All the compounds have been isolated from this plant for the first time. Compounds 1, 2 and 3 have protective effect agains MPP+ -induced apoptosis. 展开更多
关键词 iridoid glycoside Buddleja lindeyana 6-O-feruloylajugol
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UPLC/Q-TOF-MS analysis of iridoid glycosides and metabolites in rat plasma after oral administration of Paederia scandens extracts 被引量:4
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作者 WANG Dong-Mei XU Yi-Fei +2 位作者 CHEN Zhu HUANG Lin-Fang CHEN Shi-Lin 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2015年第3期215-221,共7页
A rapid and validated UPLC-MS method was developed for investigating the absorbed components of Paederia scandens(Lour.) Merrill(P.scandens) in rat plasma.The bioactive constituents in plasma samples from rats adminis... A rapid and validated UPLC-MS method was developed for investigating the absorbed components of Paederia scandens(Lour.) Merrill(P.scandens) in rat plasma.The bioactive constituents in plasma samples from rats administrated orally with P.scandens extract were analyzed by Ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry(UPLC-Q-TOF-MS).Four prototype compounds were identified in rat serum as potential bioactive components of P.scandens by comparing their retention times and mass spectrometry data or by mass spectrometry analysis and retrieving the reference literatures.Glucuronidation after deglycosylation was the major metabolic pathway for the iridoid glycosides in P.scandens.These results showed that the methods had high sensitivity and resolution and were suitable for identifying the bioactive constituents in plasma after oral administration of P.scandens.providing helpful chemical information for further pharmacological and mechanistic researched on the P.scandens. 展开更多
关键词 Paederia scandens Serum containing drug iridoid glycosides UPLC/Q-TOF-MS Absorbed components
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Two New Iridoid Glucosides from Clerodendrum serratum 被引量:2
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作者 Hui YANG Bei JIANG +2 位作者 Zhi NA Yun Pin GUO Han Dong SUN 《Chinese Chemical Letters》 SCIE CAS CSCD 2000年第3期231-234,共4页
Two new iridoid glucosides, serratoside A and serratoside B, were isolated from the aerial parts of Clerodendrum serratum var. amplexifolium Moldenke. Their structures were elucidated by spectral and chemical methods.
关键词 Clerodendrum serratum VERBENACEAE iridoid glucoside serratoside A serratoside B
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Two New Iridoid Glucosides from Clerodendrum serratum 被引量:2
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作者 Xiao Mei WEI Qi Xiou ZHU +1 位作者 Jin Chun CHEN Dong Liang CHENG (Department of Chemistry, National Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000) 《Chinese Chemical Letters》 SCIE CAS CSCD 2000年第5期415-416,共2页
Two new iridoid glucosides, named 7 beta -coumaroyloxyugandoside (1) and 7 beta - cinnamoyloxyugandoside (2) were isolated from the leaves of Clerodendrum serratum, and their structures were elucidated by spectral means.
关键词 Clerodendrum serratum VERBENACEAE iridoid glucoside 7 beta-coumaroyloxyugandoside (1). 7 beta-cinnamoyloxyugandoside (2).
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