• 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

Novel D-ring analogues of podophyllotoxin as potent anti-cancer agents.

作者信息

Subrahmanyam D, Renuka B, Rao C V, Sagar P S, Deevi D S, Babu J M, Vyas K

机构信息

Natural Products Division, Dr. Reddy's Research Foundation, Miyapur, Hyderabad, India.

出版信息

Bioorg Med Chem Lett. 1998 Jun 2;8(11):1391-6. doi: 10.1016/s0960-894x(98)00232-7.

DOI:10.1016/s0960-894x(98)00232-7
PMID:9871772
Abstract

Several D-ring modified analogues of podophyllotoxin were prepared viz semi-synthesis starting from naturally occurring podophyllotoxin and determined their in vitro anti-cancer activity. Most of the analogues have shown good activity towards human cancer cell lines.

摘要

相似文献

1
Novel D-ring analogues of podophyllotoxin as potent anti-cancer agents.
Bioorg Med Chem Lett. 1998 Jun 2;8(11):1391-6. doi: 10.1016/s0960-894x(98)00232-7.
2
Design, synthesis, and biological testing of 4beta-[(4-substituted)-1,2,3-triazol-1-yl]podophyllotoxin analogues as antitumor agents.4β-[(4-取代)-1,2,3-三唑-1-基]鬼臼毒素类似物作为抗肿瘤药物的设计、合成及生物学测试
Arch Pharm (Weinheim). 2008 Feb;341(2):126-31. doi: 10.1002/ardp.200700116.
3
9-Deoxopodophyllotoxin derivatives as anti-cancer agents.9-脱氧鬼臼毒素衍生物作为抗癌剂。
Bioorg Med Chem Lett. 1999 Aug 2;9(15):2131-4. doi: 10.1016/s0960-894x(99)00347-9.
4
Antitumor agents. Part 232: Synthesis of cyclosulfite podophyllotoxin analogues as novel prototype antitumor agents.抗肿瘤剂。第232部分:环亚硫酸酯鬼臼毒素类似物作为新型抗肿瘤剂原型的合成。
Bioorg Med Chem Lett. 2004 Mar 22;14(6):1581-4. doi: 10.1016/j.bmcl.2003.12.096.
5
Antitumor agents, 99. Synthetic ring C aromatized podophyllotoxin analogues as potential inhibitors of human DNA topoisomerase II.抗肿瘤剂,99. 合成的C环芳构化鬼臼毒素类似物作为人类DNA拓扑异构酶II的潜在抑制剂
J Nat Prod. 1988 Sep-Oct;51(5):901-5. doi: 10.1021/np50059a014.
6
Design and synthesis of C-ring lactone- and lactam-based podophyllotoxin analogues as anticancer agents.基于C环内酯和内酰胺的鬼臼毒素类似物作为抗癌剂的设计与合成
Chem Pharm Bull (Tokyo). 2010 Feb;58(2):242-6. doi: 10.1248/cpb.58.242.
7
Synthesis and cytotoxic evaluation of C-9 oxidized podophyllotoxin derivatives.C-9氧化鬼臼毒素衍生物的合成及细胞毒性评价
Bioorg Med Chem. 2007 Feb 15;15(4):1670-8. doi: 10.1016/j.bmc.2006.12.008. Epub 2006 Dec 12.
8
Synthesis and cytotoxicity of podophyllotoxin analogues modified in the A ring.A环修饰的鬼臼毒素类似物的合成及细胞毒性
Eur J Med Chem. 2003 Jan;38(1):65-74. doi: 10.1016/s0223-5234(02)00007-7.
9
[4-Aza-2,3-didehydropodophyllotoxins: new lignan with antitumor activity obtained from one-step synthesis].
Ann Pharm Fr. 2005 Jan;63(1):63-8. doi: 10.1016/s0003-4509(05)82252-7.
10
Synthesis and cytotoxicity evaluation of novel podophyllotoxin derivatives.新型鬼臼毒素衍生物的合成及细胞毒性评价。
Arch Pharm (Weinheim). 2011 Nov;344(11):735-40. doi: 10.1002/ardp.201100095. Epub 2011 Sep 2.

引用本文的文献

1
The Emerging Role of Natural Products in Cancer Treatment.天然产物在癌症治疗中的新兴作用。
Arch Toxicol. 2024 Aug;98(8):2353-2391. doi: 10.1007/s00204-024-03786-3. Epub 2024 May 25.
2
Design, Synthesis, and Biological Evaluation of SSE1806, a Microtubule Destabilizer That Overcomes Multidrug Resistance.克服多药耐药性的微管解聚剂SSE1806的设计、合成及生物学评价
ACS Med Chem Lett. 2023 Sep 8;14(10):1369-1377. doi: 10.1021/acsmedchemlett.3c00258. eCollection 2023 Oct 12.
3
Cancer Therapy Challenge: It Is Time to Look in the "St. Patrick's Well" of the Nature.
癌症治疗的挑战:是时候看看大自然的“圣帕特里克井”了。
Int J Mol Sci. 2021 Sep 26;22(19):10380. doi: 10.3390/ijms221910380.
4
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.
5
INDUCTION OF CELL CYCLE ARREST AND APOPTOSIS BY ORMENIS ERIOLEPIS A MORROCAN ENDEMIC PLANT IN VARIOUS HUMAN CANCER CELL LINES.摩洛哥特有植物毛果香青对多种人类癌细胞系的细胞周期阻滞及凋亡诱导作用
Afr J Tradit Complement Altern Med. 2017 Jan 13;14(2):356-373. doi: 10.21010/ajtcam.v14i2.37. eCollection 2017.
6
6-Methoxy Podophyllotoxin Induces Apoptosis via Inhibition of TUBB3 and TOPIIA Gene Expressions in 5637 and K562 Cancer Cell Lines.6-甲氧基鬼臼毒素通过抑制5637和K562癌细胞系中TUBB3和TOPIIA基因表达诱导细胞凋亡。
Cell J. 2015 Fall;17(3):502-9. doi: 10.22074/cellj.2015.10. Epub 2015 Oct 7.
7
Secondary metabolites as DNA topoisomerase inhibitors: A new era towards designing of anticancer drugs.作为DNA拓扑异构酶抑制剂的次生代谢产物:抗癌药物设计的新时代。
Pharmacogn Rev. 2010 Jan;4(7):12-26. doi: 10.4103/0973-7847.65320.
8
Inhibition of CYP3A4 and CYP2C9 by podophyllotoxin: implication for clinical drug-drug interactions.鬼臼毒素对 CYP3A4 和 CYP2C9 的抑制作用:对临床药物相互作用的影响。
J Biosci. 2011 Dec;36(5):879-85. doi: 10.1007/s12038-011-9143-9.
9
Natural products as leads to anticancer drugs.作为抗癌药物先导物的天然产物。
Clin Transl Oncol. 2007 Dec;9(12):767-76. doi: 10.1007/s12094-007-0138-9.
10
A high throughput drug screen based on fluorescence resonance energy transfer (FRET) for anticancer activity of compounds from herbal medicine.基于荧光共振能量转移(FRET)的高通量药物筛选,用于检测草药化合物的抗癌活性。
Br J Pharmacol. 2007 Feb;150(3):321-34. doi: 10.1038/sj.bjp.0706988. Epub 2007 Jan 18.