• 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

四苯基亚氨基甲基膦酸酯的合成及生物活性评价:作为抗氧化剂和体外破骨细胞强效抑制剂。

Synthesis and bio-activity evaluation of tetraphenyl(phenylamino) methylene bisphosphonates as antioxidant agents and as potent inhibitors of osteoclasts in vitro.

机构信息

Department of Organic Chemistry and Bio-technology, Sri Venkateswara University, Tirupati-517 502, India.

出版信息

Eur J Med Chem. 2011 May;46(5):1798-802. doi: 10.1016/j.ejmech.2011.02.038. Epub 2011 Feb 23.

DOI:10.1016/j.ejmech.2011.02.038
PMID:21397367
Abstract

A new series of tetraphenyl bisphosphonates have been elegantly synthesized by one-pot method and were characterized by elemental analysis, FTIR, 1H, 13C, 31P NMR, mass spectra and evaluated for their in vitro antibone resorptive activity by inhibiting growth of osteoclasts. Two bisphosphonates 3g and 3f showed marked inhibition ratio (8 μM and 10 μM) and emerged as lead compounds. All compounds were tested for their antioxidant (DPPH scavenging, reducing power and inhibition of lipid peroxidation). They exhibited potent in vitro antioxidant activity dose-dependently.

摘要

已通过一锅法巧妙合成了一系列新的四苯基亚膦酸酯,并通过元素分析、FTIR、1H、13C、31P NMR、质谱进行了表征,并通过抑制破骨细胞生长来评估其体外抗骨吸收活性。两种双膦酸盐 3g 和 3f 表现出明显的抑制率(8 μM 和 10 μM),并成为先导化合物。所有化合物均进行了抗氧化(DPPH 清除、还原能力和抑制脂质过氧化)测试。它们表现出与剂量相关的有效体外抗氧化活性。

相似文献

1
Synthesis and bio-activity evaluation of tetraphenyl(phenylamino) methylene bisphosphonates as antioxidant agents and as potent inhibitors of osteoclasts in vitro.四苯基亚氨基甲基膦酸酯的合成及生物活性评价:作为抗氧化剂和体外破骨细胞强效抑制剂。
Eur J Med Chem. 2011 May;46(5):1798-802. doi: 10.1016/j.ejmech.2011.02.038. Epub 2011 Feb 23.
2
A novel synthesis of 3-aryl coumarins and evaluation of their antioxidant and lipoxygenase inhibitory activity.一种新型 3-芳基香豆素的合成及其抗氧化和脂氧合酶抑制活性评价。
Bioorg Med Chem Lett. 2010 Jul 1;20(13):3889-92. doi: 10.1016/j.bmcl.2010.05.022. Epub 2010 Jun 2.
3
Synthesis of chromone carboxamide derivatives with antioxidative and calpain inhibitory properties.合成具有抗氧化和钙蛋白酶抑制活性的色酮甲酰胺衍生物。
Eur J Med Chem. 2011 May;46(5):1721-8. doi: 10.1016/j.ejmech.2011.02.025. Epub 2011 Feb 22.
4
Synthesis, spectral characterization and bioassay of 3,3'-(1,4-phenylene)-bis[2-alkoxycarbonyl-alkyl)-2-thio-benzoxa-phosphinines].3,3'-(1,4-亚苯基)-双[2-烷氧基羰基-烷基)-2-硫代苯并恶磷杂环戊烷]的合成、光谱特性和生物测定。
Eur J Med Chem. 2010 May;45(5):1828-32. doi: 10.1016/j.ejmech.2010.01.019. Epub 2010 Jan 20.
5
Antioxidant activity of newly synthesized 2,7-diazaphenothiazines.新合成的 2,7-二氮杂吩噻嗪的抗氧化活性。
Arch Pharm (Weinheim). 2010 May;343(5):268-73. doi: 10.1002/ardp.200900253.
6
Synthesis of novel amino and acetyl amino-4-methylcoumarins and evaluation of their antioxidant activity.新型氨基和乙酰氨基-4-甲基香豆素的合成及其抗氧化活性评估。
Eur J Med Chem. 2005 Apr;40(4):413-20. doi: 10.1016/j.ejmech.2004.09.002.
7
A diverse series of substituted benzenesulfonamides as aldose reductase inhibitors with antioxidant activity: design, synthesis, and in vitro activity.具有抗氧化活性的醛糖还原酶抑制剂的一系列不同取代的苯磺酰胺:设计、合成和体外活性。
J Med Chem. 2010 Nov 11;53(21):7756-66. doi: 10.1021/jm101008m.
8
Antioxydant activity of β-carboline derivatives in the LDL oxidation model.β-咔啉衍生物在 LDL 氧化模型中的抗氧化活性。
Eur J Med Chem. 2011 Jun;46(6):2575-85. doi: 10.1016/j.ejmech.2011.03.048. Epub 2011 Mar 30.
9
One-pot microwave assisted synthesis under green chemistry conditions, antioxidant screening, and cytotoxicity assessments of benzimidazole Schiff bases and pyrimido[1,2-a]benzimidazol-3(4H)-ones.一锅微波辅助法在绿色化学条件下合成、苯并咪唑席夫碱和嘧啶并[1,2-a]苯并咪唑-3(4H)-酮的抗氧化筛选和细胞毒性评估。
Eur J Med Chem. 2011 Jan;46(1):297-306. doi: 10.1016/j.ejmech.2010.11.018. Epub 2010 Nov 19.
10
Syntheses and biological activities of benzimidazolo[2,1-b] benzo[e]thiazepin-5(10H)-ones.苯并咪唑并[2,1 - b]苯并[e]硫氮杂䓬 - 5(10H) - 酮的合成及其生物活性
Arch Pharm (Weinheim). 2008 Jan;341(1):49-54. doi: 10.1002/ardp.200700099.

引用本文的文献

1
One-Pot and Catalyst-Free Transformation of -Protected 1-Amino-1-Ethoxyalkylphosphonates into Bisphosphonic Analogs of Protein and Non-Protein α-Amino Acids.一锅法无催化剂转化保护的 1-氨基-1-乙氧烷基膦酸酯为蛋白质和非蛋白质α-氨基酸的双膦酸类似物。
Molecules. 2022 Jun 2;27(11):3571. doi: 10.3390/molecules27113571.
2
Applications of alkyl orthoesters as valuable substrates in organic transformations, focusing on reaction media.原酸酯作为有机转化中有价值的底物的应用,重点关注反应介质。
RSC Adv. 2020 Aug 17;10(51):30314-30397. doi: 10.1039/d0ra05276k.
3
Bisphosphonates: The role of chemistry in understanding their biological actions and structure-activity relationships, and new directions for their therapeutic use.
双膦酸盐:化学在理解其生物学作用和构效关系以及治疗用途的新方向中的作用。
Bone. 2022 Mar;156:116289. doi: 10.1016/j.bone.2021.116289. Epub 2021 Dec 8.
4
Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties.含吡咯部分的新型 N-芳基膦酸酯及其生态毒理学性质。
Molecules. 2017 Jul 7;22(7):1132. doi: 10.3390/molecules22071132.
5
A new method for the synthesis of α-aminoalkylidenebisphosphonates and their asymmetric phosphonyl-phosphinyl and phosphonyl-phosphinoyl analogues.一种合成α-氨基亚烷基双膦酸酯及其不对称磷酰基-膦基和磷酰基-磷酰氧基类似物的新方法。
Beilstein J Org Chem. 2015 Aug 13;11:1418-24. doi: 10.3762/bjoc.11.153. eCollection 2015.