Kiamycin, a Unique Cytotoxic Angucyclinone Derivative from a Marine Streptomyces sp. | |
Xie, Zeping1,2; Liu, Bing1; Wang, Hongpeng3; Yang, Shengxiang4; Zhang, Hongyu1,2; Wang, Yipeng1![]() ![]() ![]() | |
刊名 | MARINE DRUGS
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2012-03-01 | |
卷号 | 10期号:3页码:551-558 |
关键词 | Angucyclinone Epoxybenz[a]Anthracene Marine Streptomyces Cytotoxicity |
ISSN号 | 1660-3397 |
通讯作者 | Qin, S (reprint author), Chinese Acad Sci, Yantai Inst Coastal Zone Res, Yantai 264003, Peoples R China. zpxie@yic.ac.cn ; bliu@yic.ac.cn ; wanghongpeng@hotmail.com ; ysx19821028@yahoo.com.cn ; hyzhang@yic.ac.cn ; ypwang@yic.ac.cn ; nyji@yic.ac.cn ; sqin@yic.ac.cn ; hlaatsc@gwdg.de |
产权排序 | [Xie, Zeping; Liu, Bing; Zhang, Hongyu; Wang, Yipeng; Ji, Naiyun; Qin, Song] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Yantai 264003, Peoples R China; [Xie, Zeping; Zhang, Hongyu] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China; [Wang, Hongpeng; Laatsch, Hartmut] Univ Gottingen, Dept Organ & Biomol Chem, D-37077 Gottingen, Germany; [Yang, Shengxiang] NW A&F Univ, Chem Biol Res Inst, Coll Sci, Yangling 712100, Peoples R China |
文献子类 | Article |
英文摘要 | Kiamycin (1), a new angucyclinone derivative possessing an 1,12-epoxybenz[a]anthracene ring system, was isolated from the marine Streptomyces sp. strain M268 along with the known compounds 8-O-methyltetrangomycin (3) and 8-O-methylrabelomycin (4). Their structures were elucidated by detailed spectroscopic analysis and comparison with literature data. The new angucyclinone derivative showed inhibitory activities against the human cell lines HL-60 (leukemia), A549 (lung adenocarcinoma), and BEL-7402 (hepatoma) with inhibition rates of 68.2%, 55.9%, and 31.7%, respectively, at 100 mu M. It appears to have potential as an anticancer agent with selective activity.; Kiamycin (1), a new angucyclinone derivative possessing an 1,12-epoxybenz[a]anthracene ring system, was isolated from the marine Streptomyces sp. strain M268 along with the known compounds 8-O-methyltetrangomycin (3) and 8-O-methylrabelomycin (4). Their structures were elucidated by detailed spectroscopic analysis and comparison with literature data. The new angucyclinone derivative showed inhibitory activities against the human cell lines HL-60 (leukemia), A549 (lung adenocarcinoma), and BEL-7402 (hepatoma) with inhibition rates of 68.2%, 55.9%, and 31.7%, respectively, at 100 mu M. It appears to have potential as an anticancer agent with selective activity. |
学科主题 | Pharmacology & Pharmacy |
URL标识 | 查看原文 |
WOS关键词 | ANTIBIOTICS ; PRODUCTS |
WOS研究方向 | Pharmacology & Pharmacy |
语种 | 英语 |
WOS记录号 | WOS:000302136700003 |
资助机构 | project of |
公开日期 | 2012-06-13 |
内容类型 | 期刊论文 |
源URL | [http://ir.yic.ac.cn/handle/133337/5564] ![]() |
专题 | 烟台海岸带研究所_海岸带生物学与生物资源利用所重点实验室 |
作者单位 | 1.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Yantai 264003, Peoples R China 2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China 3.Univ Gottingen, Dept Organ & Biomol Chem, D-37077 Gottingen, Germany 4.NW A&F Univ, Chem Biol Res Inst, Coll Sci, Yangling 712100, Peoples R China |
推荐引用方式 GB/T 7714 | Xie, Zeping,Liu, Bing,Wang, Hongpeng,et al. Kiamycin, a Unique Cytotoxic Angucyclinone Derivative from a Marine Streptomyces sp.[J]. MARINE DRUGS,2012,10(3):551-558. |
APA | Xie, Zeping.,Liu, Bing.,Wang, Hongpeng.,Yang, Shengxiang.,Zhang, Hongyu.,...&Laatsch, Hartmut.(2012).Kiamycin, a Unique Cytotoxic Angucyclinone Derivative from a Marine Streptomyces sp..MARINE DRUGS,10(3),551-558. |
MLA | Xie, Zeping,et al."Kiamycin, a Unique Cytotoxic Angucyclinone Derivative from a Marine Streptomyces sp.".MARINE DRUGS 10.3(2012):551-558. |
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