• 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

2-吲哚基5-(1,2,3,6-四氢吡啶基)酮的合成与抗癌筛选

Synthesis and anticancer screening of 2-indolyl 5-(1,2,3,6-tetrahydropyridyl) ketones.

作者信息

Sundberg R J, Rearick D E, Russell H F

出版信息

J Pharm Sci. 1977 Feb;66(2):263-4. doi: 10.1002/jps.2600660231.

DOI:10.1002/jps.2600660231
PMID:839425
Abstract

Several derivatives of 2-indolyl 5-(1,2,3,6-tetrahydropyridyl) ketone with various substituents on the pyridine nitrogen and with or without a benzenesulfonyl group on the indole nitrogen were synthesized and characterized by spectroscopic and analytical data. Only one showed erratic but confirmed activity in the P-388 screen. The other derivatives were inactive in the L-1210 leukemia screen.

摘要

合成了2-吲哚基5-(1,2,3,6-四氢吡啶基)酮的几种衍生物,这些衍生物在吡啶氮上带有各种取代基,吲哚氮上有或没有苯磺酰基,并通过光谱和分析数据进行了表征。只有一种在P-388筛选中显示出不稳定但已确认的活性。其他衍生物在L-1210白血病筛选中无活性。

相似文献

1
Synthesis and anticancer screening of 2-indolyl 5-(1,2,3,6-tetrahydropyridyl) ketones.2-吲哚基5-(1,2,3,6-四氢吡啶基)酮的合成与抗癌筛选
J Pharm Sci. 1977 Feb;66(2):263-4. doi: 10.1002/jps.2600660231.
2
Synthesis and cytotoxic activity of latentiated derivatives of 3-methyleneoxindole.
J Pharm Sci. 1977 Jul;66(7):1022-4. doi: 10.1002/jps.2600660732.
3
Synthesis and antineoplastic activity of phenyl-substituted benzenesulfonylhydrazones of 2-pyridinecarboxyaldehyde 1-oxide.
J Med Chem. 1980 Jun;23(6):631-4. doi: 10.1021/jm00180a010.
4
Synthesis and antitumor evaluation of novel monoindolyl-4-trifluoromethylpyridines and bisindolyl-4-trifluoromethylpyridines.新型单吲哚基-4-三氟甲基吡啶和双吲哚基-4-三氟甲基吡啶的合成与抗肿瘤评价
Bioorg Med Chem Lett. 2001 Feb 26;11(4):475-7. doi: 10.1016/s0960-894x(00)00704-6.
5
Synthesis of nitrosourea derivatives of pyridine and piperidine as potential anticancer agents.吡啶和哌啶亚硝基脲衍生物作为潜在抗癌剂的合成。
J Med Chem. 1980 Aug;23(8):848-51. doi: 10.1021/jm00182a007.
6
Synthesis and biological activity of 3- and 5-amino derivatives of pyridine-2-carboxaldehyde thiosemicarbazone.吡啶-2-甲醛缩氨基硫脲的3-氨基和5-氨基衍生物的合成及生物活性
J Med Chem. 1996 Jun 21;39(13):2586-93. doi: 10.1021/jm9600454.
7
Heterocyclic quinones. XVI. Pharmacomodulation in the series of 11H-indolo[3,2-c]quinolinediones: synthesis, cytotoxicity and antitumor activity of 3-substituted 11H-pyrido[3',4':4,5]pyrrolo[3,2-c]quinoline-1,4-diones.杂环醌。十六。11H-吲哚并[3,2-c]喹啉二酮系列中的药效调节:3-取代的11H-吡啶并[3',4':4,5]吡咯并[3,2-c]喹啉-1,4-二酮的合成、细胞毒性和抗肿瘤活性。
Chem Pharm Bull (Tokyo). 1989 Sep;37(9):2413-6. doi: 10.1248/cpb.37.2413.
8
Synthesis and biological evaluation of novel 2,6-diaminobenz[cd]indole inhibitors of thymidylate synthase using the protein structure as a guide.
J Med Chem. 1995 May 26;38(11):1892-903. doi: 10.1021/jm00011a009.
9
Synthesis of novel analogues of marine indole alkaloids: mono(indolyl)-4-trifluoromethylpyridines and bis(indolyl)-4-trifluoromethylpyridines as potential anticancer agents.海洋吲哚生物碱新型类似物的合成:单(吲哚基)-4-三氟甲基吡啶和双(吲哚基)-4-三氟甲基吡啶作为潜在的抗癌剂
Bioorg Med Chem. 2001 Jul;9(7):1773-80. doi: 10.1016/s0968-0896(01)00070-0.
10
[Cytotoxic and antitumor activity of a new series of heterocyclic compounds: dipyrido (4,3-b) (3,4-f) indoles].新型杂环化合物系列:二吡啶并(4,3 - b)(3,4 - f)吲哚的细胞毒性和抗肿瘤活性
C R Acad Hebd Seances Acad Sci D. 1977 Oct 10;285(8):945-8.