• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

来自担子菌纲真菌 Stereum sp. 子实体的羊毛甾烷三萜类化合物、结构与生物活性。

Lanostane triterpenoids from fruiting bodies of basidiomycete Stereum sp., structures and biological activities.

作者信息

Yao Jian-Neng, Chen Lin, Tang Yang, Chen He-Ping, Zhao Zhen-Zhu, Li Zheng-Hui, Feng Tao, Liu Ji-Kai

机构信息

State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China.

University of Chinese Academy of Sciences, Beijing, China.

出版信息

J Antibiot (Tokyo). 2017 Dec;70(12):1104-1111. doi: 10.1038/ja.2017.122. Epub 2017 Oct 25.

DOI:10.1038/ja.2017.122
PMID:29066792
Abstract

Twelve new lanostane triterpenoids, sterenoids A-L (1-12) have been isolated from fruiting bodies of the basidiomycete Stereum sp. Compounds 1-12 are rare 14(13→︀12)abeo-lanostane triterpenoids featuring remarkable 13R configurations that discriminate from the previously covered counterparts. Their structures and absolute configurations are assigned on the basis of in-depth one- and two-dimensional NMR spectroscopic analysis, as well as unbiased quantum chemical NMR and electronic CD calculations. All isolates are evaluated for their in vitro cytotoxicity against five human tumor cell lines. Compound 5 exhibits potent cytotoxic activities against tumor cell lines HL-60 and SMMC-7721 with IC values of 4.7 and 7.6 μM, respectively.

摘要

从担子菌纲真菌Stereum sp.的子实体中分离出了12种新的羊毛甾烷三萜类化合物,即甾体A-L(1-12)。化合物1-12是罕见的14(13→︀12)去甲羊毛甾烷三萜类化合物,具有显著的13R构型,与之前报道的同类化合物不同。它们的结构和绝对构型是基于深入的一维和二维核磁共振光谱分析,以及无偏量子化学核磁共振和电子圆二色计算确定的。对所有分离物进行了针对五种人类肿瘤细胞系的体外细胞毒性评估。化合物5对肿瘤细胞系HL-60和SMMC-7721表现出较强的细胞毒性活性,IC值分别为4.7和7.6 μM。

相似文献

1
Lanostane triterpenoids from fruiting bodies of basidiomycete Stereum sp., structures and biological activities.来自担子菌纲真菌 Stereum sp. 子实体的羊毛甾烷三萜类化合物、结构与生物活性。
J Antibiot (Tokyo). 2017 Dec;70(12):1104-1111. doi: 10.1038/ja.2017.122. Epub 2017 Oct 25.
2
Miscellaneous lanostane triterpenoids with cytotoxicities from fruiting bodies of the basidiomycete Stereum sp.从担子菌 Stereum sp. 的子实体中分离得到具有细胞毒性的多种羊毛甾烷三萜
Fitoterapia. 2018 Mar;125:227-234. doi: 10.1016/j.fitote.2017.11.020. Epub 2017 Nov 29.
3
Highly Modified Lanostane Triterpenes from Fruiting Bodies of the Basidiomycete Tomophagus sp.高度修饰的三萜类化合物来源于担子菌 Tomophagus sp. 的子实体。
J Nat Prod. 2019 May 24;82(5):1165-1176. doi: 10.1021/acs.jnatprod.8b00869. Epub 2019 Apr 15.
4
Cytotoxic lanostane triterpenoids from the fruiting bodies of Piptoporus betulinus.桦剥管菌子实体中的细胞毒性羊毛甾烷三萜类化合物。
Phytochemistry. 2017 Nov;143:98-103. doi: 10.1016/j.phytochem.2017.07.013. Epub 2017 Aug 8.
5
Two new triterpenoids from fruiting bodies of fungus Ganoderma lucidum.从灵芝子实体中分离得到的两种新三萜类化合物。
J Asian Nat Prod Res. 2015;17(7):750-5. doi: 10.1080/10286020.2014.996139. Epub 2015 Jan 29.
6
Lanostane triterpenoids with cytotoxic activities from the fruiting bodies of Ganoderma hainanense.来自海南灵芝子实体的具有细胞毒性活性的羊毛甾烷三萜类化合物。
J Asian Nat Prod Res. 2013 Nov;15(11):1214-9. doi: 10.1080/10286020.2013.820712. Epub 2013 Aug 5.
7
Antimalarial lanostane triterpenoids from cultivated fruiting bodies of the basidiomycete Ganoderma sp.从担子菌灵芝属栽培子实体中提取的抗疟羊毛甾烷三萜
J Antibiot (Tokyo). 2020 Oct;73(10):702-710. doi: 10.1038/s41429-020-0357-7. Epub 2020 Jul 30.
8
Lanostane triterpenoids from Ganoderma luteomarginatum and their cytotoxicity against four human cancer cell lines.灵芝属中的羊毛甾烷三萜及其对四种人癌细胞系的细胞毒性。
Phytochemistry. 2018 Dec;156:89-95. doi: 10.1016/j.phytochem.2018.09.003. Epub 2018 Sep 18.
9
Piptolinic acids F-J, five new lanostane-type triterpenoids from .白皮杉醇酸 F-J,五种从. 中分离得到的新型羊毛甾烷型三萜
Nat Prod Res. 2019 Nov;33(21):3044-3051. doi: 10.1080/14786419.2018.1516218. Epub 2018 Oct 26.
10
Lanostane triterpenoids from Ganoderma hainanense J. D. Zhao.来自海南灵芝(Ganoderma hainanense J. D. Zhao)的羊毛甾烷型三萜类化合物。
Phytochemistry. 2015 Jun;114:137-45. doi: 10.1016/j.phytochem.2014.10.009. Epub 2014 Oct 31.

引用本文的文献

1
Study of the Anti-MYC Potential of Lanostane-Type Triterpenes.羊毛甾烷型三萜的抗MYC潜能研究
ACS Omega. 2024 Dec 12;9(51):50844-50858. doi: 10.1021/acsomega.4c10201. eCollection 2024 Dec 24.
2
Naturally Occurring Norsteroids and Their Design and Pharmaceutical Application.天然存在的去甲甾体及其设计与药物应用。
Biomedicines. 2024 May 6;12(5):1021. doi: 10.3390/biomedicines12051021.
3
General Enantioselective and Stereochemically Divergent Four-Stage Approach to Fused Tetracyclic Terpenoid Systems.通用对映选择性和立体化学发散的四环萜烯系统的四阶段方法。

本文引用的文献

1
Determination of the Relative Configuration of Terminal and Spiroepoxides by Computational Methods. Advantages of the Inclusion of Unscaled Data.通过计算方法确定末端和螺环环氧的相对构型。未缩放数据的纳入的优势。
J Org Chem. 2017 Feb 17;82(4):1873-1879. doi: 10.1021/acs.joc.6b02129. Epub 2016 Nov 21.
2
Ostalactones A-C, β- and ε-Lactones with Lipase Inhibitory Activity from the Cultured Basidiomycete Stereum ostrea.来自栽培担子菌蚝白齿孔菌的奥塔 lactones A-C、β-和 ε-内酯及其脂肪酶抑制活性。
J Nat Prod. 2016 Dec 23;79(12):3148-3151. doi: 10.1021/acs.jnatprod.6b00647. Epub 2016 Dec 8.
3
A Short Diastereoselective Total Synthesis of (±)-Vibralactone.
J Org Chem. 2022 Mar 4;87(5):3352-3362. doi: 10.1021/acs.joc.1c02979. Epub 2022 Feb 17.
4
In Depth Natural Product Discovery from the Basidiomycetes Species.来自担子菌物种的深度天然产物发现
Microorganisms. 2020 Jul 15;8(7):1049. doi: 10.3390/microorganisms8071049.
(±)- Vibralactone 的立体选择性全合成研究进展
Org Lett. 2016 Dec 2;18(23):5971-5973. doi: 10.1021/acs.orglett.6b03007. Epub 2016 Oct 31.
4
Rearranged 6/6/5/6-Fused Triterpenoid Acids from the Stems of Kadsura coccinea.从黑老虎茎中分离得到的重排6/6/5/6-稠合三萜酸
J Nat Prod. 2016 Oct 28;79(10):2590-2598. doi: 10.1021/acs.jnatprod.6b00508. Epub 2016 Oct 5.
5
Novel Natural Oximes and Oxime Esters with a Vibralactone Backbone from the Basidiomycete Boreostereum vibrans.来自担子菌振动韧革菌的具有振动内酯骨架的新型天然肟类和肟酯类化合物。
ChemistryOpen. 2016 Jan 13;5(2):142-9. doi: 10.1002/open.201500198. eCollection 2016 Apr.
6
A Monooxygenase from Boreostereum vibrans Catalyzes Oxidative Decarboxylation in a Divergent Vibralactone Biosynthesis Pathway.从管孔菌属中筛选到的单加氧酶在结构独特的 Vibralactone 生物合成途径中催化氧化脱羧反应。
Angew Chem Int Ed Engl. 2016 Apr 25;55(18):5463-6. doi: 10.1002/anie.201510928. Epub 2016 Mar 23.
7
Natural Products as Sources of New Drugs from 1981 to 2014.1981年至2014年作为新药来源的天然产物
J Nat Prod. 2016 Mar 25;79(3):629-61. doi: 10.1021/acs.jnatprod.5b01055. Epub 2016 Feb 7.
8
Production of Useful Terpenoids by Higher-Fungus Cell Factory and Synthetic Biology Approaches.利用高等真菌细胞工厂和合成生物学方法生产有用的萜类化合物。
Trends Biotechnol. 2016 Mar;34(3):242-255. doi: 10.1016/j.tibtech.2015.12.007. Epub 2016 Jan 17.
9
Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea.可可西康定 A-F,新型生物相关的具有不同骨架的角鲨烷型三萜类化合物,来自于中国特有的植物美丽崖椒。
Org Lett. 2015 Sep 18;17(18):4616-9. doi: 10.1021/acs.orglett.5b02360. Epub 2015 Sep 8.
10
Stucturally Diverse Sesquiterpenes Produced by a Chinese Tibet Fungus Stereum hirsutum and Their Cytotoxic and Immunosuppressant Activities.中国西藏真菌密纹层孔菌产生的结构多样的倍半萜及其细胞毒性和免疫抑制活性。
Org Lett. 2015 Jun 19;17(12):3098-101. doi: 10.1021/acs.orglett.5b01356. Epub 2015 Jun 11.