MACROLIDE

作品数:32被引量:76H指数:4
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相关领域:医药卫生理学更多>>
相关作者:夏曦李少丽李建成丁双阳江海洋更多>>
相关机构:中国农业大学首都儿科研究所中国科学院更多>>
相关期刊:《Acta Pharmacologica Sinica》《Chinese Medical Journal》《Advances in Microbiology》《World Journal of Pediatrics》更多>>
相关基金:国家自然科学基金北京市自然科学基金“十一五”国家科技支撑计划The Royal Society更多>>
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Alkaloids from the endophytic fungus Penicillium brefeldianum and their cytotoxic activities被引量:4
《Chinese Chemical Letters》2017年第6期1194-1199,共6页Na Gao Zhi-Chun Shang Pei Yu Jie Luo Kai-Li Jian Ling-Yi Kong Ming-Hua Yang 
funded by the National Natural Science Foundation of China(No.81503218);the Program for Changjiang Scholars and Innovative Research Team in University(No.IRT_15R63);the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD);the Fundamental Research Funds for the Central Universities(No.2016ZZD010)
One new indoloditerpene,6,7-dehydropaxilline(1),one new indole-diketopiperazine,spirotryprostatin F(2),and one new 13-membered macrolide,N-demethylmelearoride A(3),as well as 8 known alkaloids(4-11),were isola...
关键词:Penicillium brefeldianum Alkaloids Indoloditerpene Indole-diketopiperazine 13-Membered macrolide Cytotoxicities 
A new macrolide and glycosides from the stem of Sargentodoxa cuneata被引量:4
《Chinese Chemical Letters》2009年第11期1339-1341,共3页Zhi Xian Chen Dai Lin Liu Wen Yuan Gao Tie Jun Zhang 
A new macrolide glycoside, cuneataside F was isolated from the n-butanol extract of the stem of Sargentodoxa cuneata. The structure was elucidated on the basis of extensive 1D and 2D NMR as well as HRESI-MS spectrosco...
关键词:Sargentodoxa cuneata Sargentodoxaceae GLYCOSIDES Cuneataside F 
Synthesis of novel 15-membered macrolide dimers
《Chinese Chemical Letters》2009年第8期931-934,共4页Shu Tao Ma Rui Xin Ma Rui Qing Xian Bo Jiao 
supported by the National Natural Science Foundation of China(No.2087208 1);Natural Science Foundation of Shandong(No.Y2006C3 1);Shandong Science and Technology Promotion Project(No.2005GG3202098).
A series of novel dimers of 15-membered macrolides was synthesized and evaluated. The dimers exhibited excellent activity against erythromycin-susceptible S. pneumonia, but did not show any improved activity against e...
关键词:MACROLIDE Azithromycin derivatives D/mers SYNTHESIS 
5′-Hydroxyzearalenol,a new β-resorcylic macrolide from Fusarium sp. 05ABR26被引量:1
《Chinese Chemical Letters》2008年第9期1089-1092,共4页Ling Ling Zhao Yue Gai Hisayoshi Kobayashi Chang Qi Hu Hui Ping Zhang 
the National Natural Science Foundation(No.30371680)of the People's Republic of China.
A new β-resorcylic macrolide, 5'-hydroxyzearalenol (1), was isolated from the culture broth of a marine-derived fungus Fusarium sp. 05ABR26. Three known compounds, zearalenone (2), 8'-hydroxyzearalenone (3) a...
关键词:5'-Hydroxyzearalenol Fusarium sp. X-ray diffraction data Pyricularia oryzae 
Synthesis of novel 15-membered macrolide derivatives被引量:2
《Chinese Chemical Letters》2008年第4期409-411,共3页Rui Qing Xian Shu Tao Ma Bo Jiao 
supported by NNSFC(No.20372043),Shandong Science and Technology Promotion Project(No.2005GG3202098);Natural Science Foundation of Shandong Province(No.Y2006C31).
In order to develop new antibiotics effective against resistant bacteria,a series of novel 15-membered macrolide derivatives were designed and synthesized by the modification of hydroxyl groups at C-11,C-12 and C-4" ...
关键词:MACROLIDE Azithromycin derivatives SYNTHESIS 4"-Carbamate derivatives 
Synthesis of derivatives of imidazo[4,5-b]pyridine:Novel sulfur contained side chains for macrolide antibiotics被引量:2
《Chinese Chemical Letters》2008年第1期1-4,共4页Lu Liu Peng Xu Liang Zhou Ping Sheng Lei 
Finacial support of this research by the National Natural Science Foundation of China (No. 30572275) ;Natural Science Foundation of Beijing (No. 7062047) are gratefully acknowledged by the authors.
Two series of novel derivatives of imidazo[4,5-b]pyridine were synthesized. These compounds could be used as side chains of semisynthesised ketolide antibiotics. The side chains have free amine group which can attache...
关键词:MACROLIDE Heterarylalkyl sulfur contained side chain Imidazo[4 5-b]pyridine Synthesis HMBC 
Synthesis of 12-alkoxycarbonylmethylene-1,15-pentadecanolides
《Chinese Chemical Letters》2007年第8期915-916,共2页Jian Jun Li Shu Hui Jin Xiao Mei Liang De Kai Yuan Dao Quan Wang 
Six novel 12-alkoxycarbonylmethylene-1,15-pentadecanolides (3) were synthesized from 2-nitrocyclo-dodecanone by the Michael addition with acrolein followed by ring enlargement, Nef reaction and Wittig-Homer reaction...
关键词:12-Alkoxycarbonylmethylene-1  15-pentadecanolide MACROLIDE Acrylic ester Wittig-Horner reaction Fungicidal actictity 
A Novel Oxidative N-Demethylation of 12-Membered Macrolide with Lead Tetraacetate
《Chinese Chemical Letters》2006年第1期9-11,共3页Wei Ge ZHANG Ying Hua JIN Ping QI Kai BAO Jin Guang LIN Nai Li WANG Xin Shen YAO 
Reaction of 12-membered macrolide 1 with lead tetraacetate in dichloromethane afforded an unexpected, novel oxidative N-demethyl product 3.
关键词:Oxidative N-demethylation 12-membered macrolide lead tetraacetate. 
β-Lactam Templated Macrocyclization:Synthesis of 12-Membered Macrolide
《Chinese Chemical Letters》2005年第5期601-603,共3页GuoJuanLIANG JinZhongZHANG AnQiCHEN 
This work is supported by the National Natural Science Foundation of China (grant No: 20372056);a Research Fund from the Royal Society of Chemistry. UK.
A novel macrolactonization method was developed using a chiral β-lactam as the template. This novel method features that the macrocyclization is simultaneously achieved while a TBS protected hydroxy group is deprotec...
关键词:LACTAM macrolactonization MACROLIDE templated cyclization. 
Partial Synthesis of Macrolide Alkaloid Euonine
《Chinese Chemical Letters》1998年第10期927-928,共2页Yuan Chao LI Shan Hao JIANG Xiao Yi WANG (Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 200031 Department of Environmental Chemistry and Engineering, Beijing Polytechnic University,Beijing, 100022) 
The macrolide alkaloid euonine 1 with pharmacologic activity was prepared from the alkaloid wilforgine 2. Their structures were confirmed by IR, NMR, MS and optical rotation.
关键词:TRIPTERYGIUM macrolide alkaloid wilforgin euonine 
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