• 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

鬼臼毒素的半合成、生物合成、生物活性、作用方式及构效关系综述:2003 - 2007年

A review on hemisynthesis, biosynthesis, biological activities, mode of action, and structure-activity relationship of podophyllotoxins: 2003-2007.

作者信息

Xu Hui, Lv Min, Tian Xuan

机构信息

Laboratory of Pharmaceutical Synthesis, College of Science, Northwest A&F University, Yangling 712100, P. R. China.

出版信息

Curr Med Chem. 2009;16(3):327-49. doi: 10.2174/092986709787002682.

DOI:10.2174/092986709787002682
PMID:19149581
Abstract

Podophyllotoxin is an important and much sought after antimitotic natural lead compound, since it paved the way for three hemisynthetic derivatives of podophyllotoxin, e.g., etoposide, teniposide and etopophos, which are widely used as anticancer drugs and show good clinical effects against several types of neoplasms. Although the publication of the recent reviews by Gordaliza in 2004 and You in 2005, which covered the literatures concerning podophyllotoxin until the early part of 2003, there have been significant number of works carried out on podophyllotoxin recently. Therefore, this review presents up-to-date coverage of podophyllotoxin in regard to hemisynthesis, biosynthesis, biological activities, mode of action and structure-activity relationship.

摘要

鬼臼毒素是一种重要且备受追捧的抗有丝分裂天然先导化合物,因为它为三种鬼臼毒素的半合成衍生物铺平了道路,例如依托泊苷、替尼泊苷和依托泊磷,这些衍生物被广泛用作抗癌药物,对几种类型的肿瘤显示出良好的临床效果。尽管Gordaliza在2004年和You在2005年发表了近期综述,涵盖了截至2003年初有关鬼臼毒素的文献,但最近对鬼臼毒素开展了大量研究工作。因此,本综述提供了鬼臼毒素在半合成、生物合成、生物活性、作用方式和构效关系方面的最新内容。

相似文献

1
A review on hemisynthesis, biosynthesis, biological activities, mode of action, and structure-activity relationship of podophyllotoxins: 2003-2007.鬼臼毒素的半合成、生物合成、生物活性、作用方式及构效关系综述:2003 - 2007年
Curr Med Chem. 2009;16(3):327-49. doi: 10.2174/092986709787002682.
2
Recent advances in semisynthesis, biosynthesis, biological activities, mode of action, and structure-activity relationship of podophyllotoxins: an update (2008-2010).近年来鬼臼毒素的半合成、生物合成、生物活性、作用模式和构效关系的研究进展:更新(2008-2010)。
Mini Rev Med Chem. 2011 Sep;11(10):901-9. doi: 10.2174/138955711796575461.
3
Discovery of podophyllotoxins.鬼臼毒素的发现。
Biochimie. 1998 Mar;80(3):207-22. doi: 10.1016/s0300-9084(98)80004-7.
4
Podophyllotoxin: distribution, sources, applications and new cytotoxic derivatives.鬼臼毒素:分布、来源、应用及新型细胞毒性衍生物
Toxicon. 2004 Sep 15;44(4):441-59. doi: 10.1016/j.toxicon.2004.05.008.
5
Recent developments towards podophyllotoxin congeners as potential apoptosis inducers.鬼臼毒素类似物作为潜在凋亡诱导剂的最新进展。
Anticancer Agents Med Chem. 2015;15(5):565-74. doi: 10.2174/1871520614666141130125623.
6
Antitumor properties of podophyllotoxin and related compounds.鬼臼毒素及相关化合物的抗肿瘤特性。
Curr Pharm Des. 2000 Dec;6(18):1811-39. doi: 10.2174/1381612003398582.
7
Synthetic and application perspectives of azapodophyllotoxins: alternative scaffolds of podophyllotoxin.氮杂鬼臼毒素的合成与应用前景:鬼臼毒素的替代支架。
Curr Med Chem. 2011;18(25):3853-70. doi: 10.2174/092986711803414331.
8
Recent progress on C-4-modified podophyllotoxin analogs as potent antitumor agents.C-4修饰的鬼臼毒素类似物作为强效抗肿瘤药物的最新进展。
Med Res Rev. 2015 Jan;35(1):1-62. doi: 10.1002/med.21319. Epub 2014 May 14.
9
Podophyllotoxin derivatives: current synthetic approaches for new anticancer agents.鬼臼毒素衍生物:新型抗癌药物的当前合成方法
Curr Pharm Des. 2005;11(13):1695-717. doi: 10.2174/1381612053764724.
10
Cytotoxic cyclolignans related to podophyllotoxin.与鬼臼毒素相关的细胞毒性环木脂素。
Farmaco. 2001 Apr;56(4):297-304. doi: 10.1016/s0014-827x(01)01030-8.

引用本文的文献

1
Crystal Structures of d-Lyxono-1,4-lactone and Its -Tosyl Derivative.d-来苏糖-1,4-内酯及其对甲苯磺酰衍生物的晶体结构
Molecules. 2025 Jan 13;30(2):287. doi: 10.3390/molecules30020287.
2
Asymmetric Migratory Tsuji-Wacker Oxidation Enables the Enantioselective Synthesis of Hetero- and Isosteric Diarylmethanes.不对称迁移的辻-瓦克氧化反应实现了杂芳基和等排二芳基甲烷的对映选择性合成。
J Am Chem Soc. 2024 Dec 18;146(50):34383-34393. doi: 10.1021/jacs.4c09405. Epub 2024 Dec 7.
3
Tandem Hock and Friedel-Crafts reactions allowing an expedient synthesis of a cyclolignan-type scaffold.
串联霍克反应和傅克反应实现了环木脂素型骨架的便捷合成。
Beilstein J Org Chem. 2024 Jan 25;20:162-169. doi: 10.3762/bjoc.20.15. eCollection 2024.
4
Synthesis of Ketonylated Carbocycles via Excited-State Copper-Catalyzed Radical Carbo-Aroylation of Unactivated Alkenes.通过激发态铜催化未活化烯烃的自由基碳芳基化反应合成酮基化碳环化合物
ChemCatChem. 2023 Jan 9;15(1). doi: 10.1002/cctc.202201128. Epub 2022 Dec 13.
5
Podophyllotoxin reduces the aggressiveness of human oral squamous cell carcinoma through myeloid cell leukemia‑1.鬼臼毒素通过髓样细胞白血病-1 降低人口腔鳞状细胞癌的侵袭性。
Int J Mol Med. 2023 Nov;52(5). doi: 10.3892/ijmm.2023.5306. Epub 2023 Sep 15.
6
Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins.天然和结构修饰的鬼臼毒素的化学和生物学活性。
Molecules. 2022 Dec 30;28(1):302. doi: 10.3390/molecules28010302.
7
A new host-targeted antiviral cyclolignan (SAU-22.107) for Dengue Virus infection in cell cultures. Potential action mechanisms based on cell imaging.一种新的针对宿主的抗病毒环木脂素(SAU-22.107)可用于细胞培养中的登革热病毒感染。基于细胞成像的潜在作用机制。
Virus Res. 2023 Jan 2;323:198995. doi: 10.1016/j.virusres.2022.198995. Epub 2022 Nov 4.
8
In Vitro Anti-Tubulin Activity on MCF10A Cell Line and In Silico Rigid/Semiflexible-Residues Docking, of Two Lignans from Bursera Fagaroides var. Fagaroides.体外 MCF10A 细胞系抗微管蛋白活性及两种来自黄胆树(Bursera fagaroides var. fagaroides)的木脂素的刚性/半刚性残基对接的计算机模拟。
Molecules. 2021 Oct 12;26(20):6155. doi: 10.3390/molecules26206155.
9
Podophyllotoxin: History, Recent Advances and Future Prospects.鬼臼毒素:历史、最新进展及未来展望。
Biomolecules. 2021 Apr 19;11(4):603. doi: 10.3390/biom11040603.
10
A Review of the Pharmacological Activities and Recent Synthetic Advances of γ-Butyrolactones.γ-丁内酯的药理活性及近期合成进展综述。
Int J Mol Sci. 2021 Mar 9;22(5):2769. doi: 10.3390/ijms22052769.