• 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

新型芳基亚甲基双异恶唑[4,5-b]吡啶-N-氧化物的多组分合成及体外和体内抗癌活性。

Multi-component synthesis and in vitro and in vivo anticancer activity of novel arylmethylene bis-isoxazolo[4,5-b]pyridine-N-oxides.

机构信息

Department of Chemistry, Kakatiya University, Vidyaranyapuri, Warangal, A.P. 506 009, India.

出版信息

Eur J Med Chem. 2012 Apr;50:274-9. doi: 10.1016/j.ejmech.2012.02.004. Epub 2012 Feb 10.

DOI:10.1016/j.ejmech.2012.02.004
PMID:22377593
Abstract

A three component one-pot protocol has been investigated for the synthesis of arylmethylene bis-isoxazolo[4,5-b]pyridine-N-oxides 1 from the commercially available materials. The title compounds 1 were also synthesized by a step-wise method and found to be identical with one-pot synthesis by spectral and analytical data. The newly synthesized compounds were evaluated for their in vitro anticancer activity against human cancer cell lines and in vivo anticancer activity on EAC-bearing mice. Compound 1a was found to be the most active both in in vitro and in vivo cytotoxic studies.

摘要

已经研究了一种三组分一锅法,从市售材料合成芳基亚甲基双异恶唑并[4,5-b]吡啶-N-氧化物 1。标题化合物 1 也通过逐步法合成,并通过光谱和分析数据发现与一锅合成相同。新合成的化合物对其在体外对人类癌细胞系的抗癌活性和在 EAC 荷瘤小鼠体内的抗癌活性进行了评估。在体外和体内细胞毒性研究中,化合物 1a 被发现是最活跃的。

相似文献

1
Multi-component synthesis and in vitro and in vivo anticancer activity of novel arylmethylene bis-isoxazolo[4,5-b]pyridine-N-oxides.新型芳基亚甲基双异恶唑[4,5-b]吡啶-N-氧化物的多组分合成及体外和体内抗癌活性。
Eur J Med Chem. 2012 Apr;50:274-9. doi: 10.1016/j.ejmech.2012.02.004. Epub 2012 Feb 10.
2
Design, synthesis, in vitro antimicrobial and anticancer activity of novel methylenebis-isoxazolo[4,5-b]azepines derivatives.新型亚甲基双异恶唑并[4,5-b]氮杂卓衍生物的设计、合成及体外抗菌和抗癌活性。
Eur J Med Chem. 2012 Apr;50:344-9. doi: 10.1016/j.ejmech.2012.02.013. Epub 2012 Feb 13.
3
Synthesis and biological evaluation of novel triazoles and isoxazoles linked 2-phenyl benzothiazole as potential anticancer agents.新型三唑并异恶唑连接 2-苯基苯并噻唑的合成及生物评价作为潜在的抗癌剂。
Bioorg Med Chem Lett. 2012 Sep 1;22(17):5424-7. doi: 10.1016/j.bmcl.2012.07.041. Epub 2012 Jul 17.
4
Synthesis and in vitro and in vivo anticancer activity of novel 3-methyl-5H-isoxazolo[5',4':5,6]pyrido[2,3-b]indoles.新型 3-甲基-5H-异恶唑并[5',4':5,6]吡啶并[2,3-b]吲哚的合成及体外和体内抗癌活性。
Bioorg Med Chem Lett. 2012 Nov 1;22(21):6677-80. doi: 10.1016/j.bmcl.2012.08.098. Epub 2012 Sep 13.
5
Efficient regioselective synthesis and potential antitumor evaluation of isoxazolo[5,4-b]pyridines and related annulated compounds.高效区域选择性合成异恶唑并[5,4-b]吡啶及其相关稠合化合物,并评估其潜在的抗肿瘤活性。
Arch Pharm (Weinheim). 2012 Jun;345(6):468-75. doi: 10.1002/ardp.201100258. Epub 2012 Mar 2.
6
Synthesis and cytotoxic activities of 4,5-diarylisoxazoles.4,5-二芳基异恶唑的合成及细胞毒性活性
Bioorg Med Chem Lett. 2007 Feb 15;17(4):1078-81. doi: 10.1016/j.bmcl.2006.11.023. Epub 2006 Nov 10.
7
The synthesis of 3,5,6,7-tetrasubstituted isoxazolo[4,5-b]pyridines and an evaluation of their in vitro antiproliferative activity.3,5,6,7-四取代异噁唑并[4,5-b]吡啶的合成及其体外抗增殖活性评价。
Adv Clin Exp Med. 2012 Sep-Oct;21(5):563-71.
8
Synthesis and antiproliferative activity in vitro of new 3-substituted aminoisoxazolo[5,4-b]pyridines.新型3-取代氨基异恶唑并[5,4-b]吡啶的体外合成及其抗增殖活性
Acta Pol Pharm. 2003 Jul-Aug;60(4):293-301.
9
Synthesis and in-vitro anticancer activity of 3,5-bis(indolyl)-1,2,4-thiadiazoles.3,5-双(吲哚基)-1,2,4-噻二唑的合成及其体外抗癌活性。
Bioorg Med Chem Lett. 2011 Oct 1;21(19):5897-900. doi: 10.1016/j.bmcl.2011.07.089. Epub 2011 Jul 30.
10
Antitumor activity of imidazothioxanthones in murine and human tumor models in vitro and in vivo.咪唑并噻吨酮在小鼠和人类肿瘤模型中的体内外抗肿瘤活性。
Anticancer Res. 2004 Mar-Apr;24(2B):907-19.

引用本文的文献

1
Mild and efficient synthesis and base-promoted rearrangement of novel isoxazolo[4,5-]pyridines.新型异恶唑并[4,5 -]吡啶的温和高效合成及碱促进重排反应
Beilstein J Org Chem. 2024 May 14;20:1069-1075. doi: 10.3762/bjoc.20.94. eCollection 2024.
2
Dihydropyrimidinones: efficient one-pot green synthesis using Montmorillonite-KSF and evaluation of their cytotoxic activity.二氢嘧啶酮:使用蒙脱石-KSF的高效一锅法绿色合成及其细胞毒性活性评估
RSC Adv. 2020 Nov 23;10(69):42221-42234. doi: 10.1039/d0ra09072g. eCollection 2020 Nov 17.
3
One-pot synthesis, biological evaluation and molecular docking studies of fused thiazolo[2,3-b]pyrimidinone-pyrazolylcoumarin hybrids.
一锅法合成、生物评价及融合噻唑并[2,3-b]嘧啶-吡唑并香豆素杂合体系的分子对接研究。
Mol Divers. 2018 Nov;22(4):943-956. doi: 10.1007/s11030-018-9845-0. Epub 2018 Jul 2.
4
2-(4-Bromo-phen-yl)-4-(4-meth-oxy-phen-yl)-6,7,8,9-tetra-hydro-5H-cyclo-hepta-[b]pyridine.2-(4-溴苯基)-4-(4-甲氧基苯基)-6,7,8,9-四氢-5H-环庚并[b]吡啶
Acta Crystallogr Sect E Struct Rep Online. 2013 May 25;69(Pt 6):o956. doi: 10.1107/S1600536813013913. Print 2013 Jun 1.