Tripodalsporormielones A-C,unprecedented cage-like polyketides with complex polyvdent bridged and fu

来源 :药学学报(英文版) | 被引量 : 0次 | 上传用户:yanhe100
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
A chemical investigation on Sporormiella sp.led to the isolation and structural elucidation of tripodalsporormielones A-C(1-3),a new class of polyketide possessing unprecedented cage-like skel-etons with polyvdent bridged and fused ring systems.These polyketides with cage-like skeletons were characterized as a high non-protonated carbon-containing system,which resulted in few HMBC correla-tions observed and made the accurate structures hard to be obtained by NMR.Especially,some signals of non-protonated sp2 carbons are weak and even unobservable in compound 1.In order to establish the structure of 1,the calculated NMR with DP4 evaluation was applied to determine the structure from the plausible structure candidates obtained from the detailed NMR analysis.Based on NMR experiments and calculated NMR,the structures of isolated compounds were established and confirmed by X-ray tech-nology.Through chiral isolation,the optically pure enantiomers of 1 and 3 were obtained,and their ab-solute configurations were determined based on ECD quantum chemical calculation.Based on the isolated compounds and our previous work,1-3 would be derived from 3-methylorcinaldehyde,and their plausible biosynthetic mechanism was proposed.Furthermore,1 exhibited obvious short-term memory improvement activity on an Alzheimer\'s disease fly model.
其他文献
苏州,明清时期我国“制造业”的中心城市rn清乾隆十一年(公元1 746年),纳兰常安正处于自己仕途的巅峰.在历任太原府通判、冀宁道、山西粮驿道、广西按察使、云南布政使、江西巡抚、盛京兵部侍郎、刑部侍郎、漕运总督后,他在浙江巡抚的位置上己任职5年.多年来宦海沉浮、游历四方的经历,让他领略了各地不同的舆地风土,见识了诸多奇闻异事,他将这些内容都写入了自己的著作《受宜堂宦游笔记》之中.在所到过的诸地中,有一处城市之繁华、商贸之兴盛、物产之精美,令他叹为观止:他写到苏州“制造百物”:“苏州专诸巷,琢玉、雕金、镂木
期刊
Although primary vesical calculi is an ancient disease,the mechanism of calculi formation remains unclear.In this study,we established a novel primary vesical calculi model with D,L-choline tartrate in mice.Compared with commonly used melamine and ethylen
Tumor cells have unique metabolic programming that is biologically distinct from that of corresponding normal cells.Resetting tumor metabolic programming is a promising strategy to amelio-rate drug resistance and improve the tumor microenvironment.Here,we
“放心!你一定不会错过它,这就像是你走在路上,用余光瞥到了一只独角兽.鬼笔就是真菌里的非主流,一个个都穿着奇装异服,只需一眼,你就无法忽视它的存在.”这是江苏省中国科学院植物研究所的郑玉红老师带我在南京植物园里寻找鬼笔时说的话.rn鬼笔是大型真菌(子实体肉眼可见的真菌)中的一类,听名字就知道它们不是籍籍无名的角色.古人觉得它们的菌盖形似毛笔,其上往往还包裹着深色的黏液,如同蘸了墨汁一般,故以鬼笔命名.在我国最早关于鬼笔的记载出现于唐代,在中药学家陈藏器写的药物学名著《本草拾遗》中,就有对它的描述:“鬼笔生
期刊
Bile acids(BAs)are amphipathic molecules important for metabolism of cholesterol,absorp-tion of lipids and lipid soluble vitamins,bile flow,and regulation of gut microbiome.There are over 30 different BA species known to exist in humans and mice,which are
An essential step for cancer vaccination is to break the immunosuppression and elicit a tumor-specific immunity.A major hurdle against cancer therapeutic vaccination is the insufficient im-mune stimulation of the cancer vaccines and lack of a safe and eff
Drug transportation is impeded by various barriers in the hypoxic solid tumor,resulting in compromised anticancer efficacy.Herein,a solid lipid monostearin(MS)-coated CaO2/MnO2 nanocarrier was designed to optimize doxorubicin(DOX)transportation comprehens
Glioblastoma is carcinogenesis of glial cells in central nervous system and has the highest incidence among primary brain tumors.Brain metastasis,such as breast cancer and lung cancer,also leads to high mortality.The available medicines are limited due to
The bile acid-responsive G-protein-coupled receptor TGR5 is expressed in monocytes and macrophages,and plays a critical role in regulating inflammatory response.Our previous work has shown its role in promoting the progression of non-small cell lung cance
Disease-mediated alterations to drug disposition constitute a significant source of adverse drug reactions.Cisplatin(CDDP)elicits nephrotoxicity due to exposure in proximal tubule cells during renal secretion.Alterations to renal drug transporter expressi