• 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

Synthesis and antitumor activity of triazolium-bis(triazole)-tetrachlororuthenate (III) and bistriazolium-triazolepentachlororuthenate (III). Two representatives of a new class of inorganic antitumor agents.

作者信息

Keppler B K, Balzer W, Seifried V

机构信息

Anorganisch-Chemisches Institut, Universität Heidelberg, Fed. Rep. of Germany.

出版信息

Arzneimittelforschung. 1987 Jul;37(7):770-1.

PMID:3675670
Abstract

The synthesis of the two water-soluble heterocycle coordinated ruthenium complexes triazolium-bis(triazole) tetrachlororuthenate (III), TrH(RuTr2Cl4), and bistriazolium-triazolepentachlororuthenate (III), (TrH)2(RuTrCl5), is described. For these complexes, antitumor activity against the P 388 leukemia model was observed with T/C values of 137% to 150%, compared with 144% and 175% for 5-fluorouracil and cisplatin, respectively. These complexes belong to a new class of antitumor active ruthenium compounds with the general formulas HB(RuB2Cl4) and (HB) 2(RuBCl5). The here described complexes with B = triazole are less active than the same type of complexes with B = imidazole, which were described by us previously.

摘要

相似文献

1
Synthesis and antitumor activity of triazolium-bis(triazole)-tetrachlororuthenate (III) and bistriazolium-triazolepentachlororuthenate (III). Two representatives of a new class of inorganic antitumor agents.
Arzneimittelforschung. 1987 Jul;37(7):770-1.
2
Structure-activity relationships for NAMI-A-type complexes (HL)[trans-RuCl4L(S-dmso)ruthenate(III)] (L = imidazole, indazole, 1,2,4-triazole, 4-amino-1,2,4-triazole, and 1-methyl-1,2,4-triazole): aquation, redox properties, protein binding, and antiproliferative activity.NAMI-A型配合物(HL)[反式-四氯钌(III)L(S-二甲基亚砜)](L =咪唑、吲唑、1,2,4-三唑、4-氨基-1,2,4-三唑和1-甲基-1,2,4-三唑)的构效关系:水合作用、氧化还原性质、蛋白质结合及抗增殖活性
J Med Chem. 2007 May 3;50(9):2185-93. doi: 10.1021/jm061081y. Epub 2007 Apr 3.
3
Preclinical evaluation of dichlorobis(1-phenylbutane-1,3-dionato)titanium (IV) and budotitane. Two representatives of the new class of antitumor-active bis-beta-diketonato metal complexes.
Arzneimittelforschung. 1986 Dec;36(12):1822-8.
4
Tuning of redox potentials for the design of ruthenium anticancer drugs -- an electrochemical study of [trans-RuCl(4)L(DMSO)](-) and [trans-RuCl(4)L(2)](-) complexes, where L = imidazole, 1,2,4-triazole, indazole.用于设计钌抗癌药物的氧化还原电位调节——[反式-RuCl₄L(DMSO)]⁻和[反式-RuCl₄L₂]⁻配合物的电化学研究,其中L = 咪唑、1,2,4-三唑、吲唑
Inorg Chem. 2004 Nov 1;43(22):7083-93. doi: 10.1021/ic049479c.
5
Antitumor activity of imidazolium-bisimidazole-tetrachlororuthenate (III). A representative of a new class of inorganic antitumor agents.咪唑鎓 - 双咪唑 - 四氯钌(III)的抗肿瘤活性。一类新型无机抗肿瘤剂的代表。
J Cancer Res Clin Oncol. 1986;111(2):166-8. doi: 10.1007/BF00400758.
6
Studies of rhenium carboxylates as antitumor agents. Part II. Antitumor studies of bis (mu-propionato) diaquotetrabromodirhenium (III) in tumor-bearing mice.羧基铼作为抗肿瘤剂的研究。第二部分。双(μ-丙酸根)二水四溴二铼(III)对荷瘤小鼠的抗肿瘤研究。
Methods Find Exp Clin Pharmacol. 1983 Sep;5(7):435-8.
7
In vivo antitumor activity and in vitro cytotoxic properties of bis[1,2-bis(diphenylphosphino)ethane]gold(I) chloride.二氯双[1,2-双(二苯基膦基)乙烷]金(I)的体内抗肿瘤活性和体外细胞毒性特性
Cancer Res. 1986 Nov;46(11):5486-93.
8
Synthesis, characterization, toxicity, cytogenetic and in vivo antitumor studies of 1,1-dithiolate Cu(II) complexes with di-, tri-, tetra- amines and 1,3-thiazoles. Structure-activity correlation.含二胺、三胺、四胺和1,3-噻唑的1,1-二硫醇铜(II)配合物的合成、表征、毒性、细胞遗传学及体内抗肿瘤研究。构效关系。
Bioorg Med Chem. 2009 Apr 15;17(8):3142-51. doi: 10.1016/j.bmc.2009.02.059. Epub 2009 Mar 5.
9
Synthesis, structural characterization, solution chemistry, and preliminary biological studies of the ruthenium(III) complexes [TzH][trans-RuCl4(Tz)2] and [TzH][trans-RuCl4(DMSO)(Tz)].(DMSO), the thiazole analogues of antitumor ICR and NAMI-A.钌(III)配合物[TzH][反式-RuCl4(Tz)2]和[TzH][反式-RuCl4(DMSO)(Tz)].(DMSO)的合成、结构表征、溶液化学及初步生物学研究,这两种配合物是抗肿瘤药物ICR和NAMI-A的噻唑类似物 。
Inorg Chem. 2004 Jun 28;43(13):3863-70. doi: 10.1021/ic0354116.
10
New cytotoxic and water-soluble bis(2-phenylazopyridine)ruthenium(II) complexes.新型细胞毒性水溶性双(2-苯基偶氮吡啶)钌(II)配合物
J Med Chem. 2003 Apr 24;46(9):1743-50. doi: 10.1021/jm021110e.

引用本文的文献

1
A ruthenium anticancer compound interacts with histones and impacts differently on epigenetic and death pathways compared to cisplatin.一种钌抗癌化合物与组蛋白相互作用,与顺铂相比,对表观遗传和死亡途径的影响有所不同。
Oncotarget. 2017 Jan 10;8(2):2568-2584. doi: 10.18632/oncotarget.13711.
2
In vitro and in vivo activity and cross resistance profiles of novel ruthenium (II) organometallic arene complexes in human ovarian cancer.新型钌(II)有机金属芳烃配合物在人卵巢癌中的体外和体内活性及交叉耐药谱
Br J Cancer. 2002 May 20;86(10):1652-7. doi: 10.1038/sj.bjc.6600290.