• 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

相似文献

1
Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.5'-(((Z)-4-氨基-2-丁烯基)甲基氨基)-5'-脱氧腺苷(MDL 73811,或AbeAdo)类似物的合成与评价——一种具有抗锥虫活性的S-腺苷甲硫氨酸脱羧酶抑制剂
Bioorg Med Chem. 2017 Oct 15;25(20):5433-5440. doi: 10.1016/j.bmc.2017.07.063. Epub 2017 Aug 3.
2
Novel S-adenosylmethionine decarboxylase inhibitors for the treatment of human African trypanosomiasis.用于治疗人类非洲锥虫病的新型S-腺苷甲硫氨酸脱羧酶抑制剂。
Antimicrob Agents Chemother. 2009 May;53(5):2052-8. doi: 10.1128/AAC.01674-08. Epub 2009 Mar 16.
3
Antitrypanosomal effects of polyamine biosynthesis inhibitors correlate with increases in Trypanosoma brucei brucei S-adenosyl-L-methionine.多胺生物合成抑制剂的抗锥虫作用与布氏布氏锥虫中S-腺苷-L-甲硫氨酸的增加相关。
Biochem J. 1991 Mar 1;274 ( Pt 2)(Pt 2):527-33. doi: 10.1042/bj2740527.
4
Synthesis and evaluation of analogues of 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine as inhibitors of tumor cell growth, trypanosomal growth, and HIV-1 infectivity.5'-([(Z)-4-氨基-2-丁烯基]甲基氨基)-5'-脱氧腺苷类似物作为肿瘤细胞生长、锥虫生长和HIV-1感染性抑制剂的合成与评价
J Med Chem. 2002 Nov 7;45(23):5112-22. doi: 10.1021/jm0201621.
5
Identification of Trypanosoma brucei AdoMetDC Inhibitors Using a High-Throughput Mass Spectrometry-Based Assay.使用基于高通量质谱的检测方法鉴定布氏锥虫腺苷甲硫氨酸脱羧酶抑制剂
ACS Infect Dis. 2017 Jul 14;3(7):512-526. doi: 10.1021/acsinfecdis.7b00022. Epub 2017 Apr 7.
6
Trypanocidal activity of 8-methyl-5'-{[(Z)-4-aminobut-2-enyl]-(methylamino)}adenosine (Genz-644131), an adenosylmethionine decarboxylase inhibitor.8-甲基-5'-{[(Z)-4-氨基丁-2-烯基]-(甲氨基)}腺苷(Genz-644131)的杀锥虫活性,一种腺苷甲硫氨酸脱羧酶抑制剂
Antimicrob Agents Chemother. 2009 Aug;53(8):3269-72. doi: 10.1128/AAC.00076-09. Epub 2009 May 18.
7
Discovery of new S-adenosylmethionine decarboxylase inhibitors for the treatment of Human African Trypanosomiasis (HAT).发现用于治疗人类非洲锥虫病(HAT)的新型S-腺苷甲硫氨酸脱羧酶抑制剂。
Bioorg Med Chem Lett. 2009 Jun 1;19(11):2916-9. doi: 10.1016/j.bmcl.2009.04.096. Epub 2009 Apr 24.
8
Uptake of the antitrypanosomal drug 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine (MDL 73811) by the purine transport system of Trypanosoma brucei brucei.布氏布氏锥虫的嘌呤转运系统对抗锥虫药物5'-([(Z)-4-氨基-2-丁烯基]甲基氨基)-5'-脱氧腺苷(MDL 73811)的摄取。
Biochem J. 1992 May 1;283 ( Pt 3)(Pt 3):755-8. doi: 10.1042/bj2830755.
9
Structure-activity relationships of synthetic cordycepin analogues as experimental therapeutics for African trypanosomiasis.合成虫草素类似物作为抗非洲锥虫病实验治疗药物的构效关系。
J Med Chem. 2013 Dec 27;56(24):9861-73. doi: 10.1021/jm401530a. Epub 2013 Dec 10.
10
Polyamine-mediated regulation of S-adenosylmethionine decarboxylase expression in mammalian cells. Studies using 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine, a suicide inhibitor of the enzyme.多胺对哺乳动物细胞中S-腺苷甲硫氨酸脱羧酶表达的调节作用。使用该酶的自杀性抑制剂5'-([(Z)-4-氨基-2-丁烯基]甲基氨基)-5'-脱氧腺苷进行的研究。
Eur J Biochem. 1993 Jun 15;214(3):671-6. doi: 10.1111/j.1432-1033.1993.tb17967.x.

引用本文的文献

1
Polyamine Metabolism for Drug Intervention in Trypanosomatids.用于锥虫药物干预的多胺代谢
Pathogens. 2024 Jan 16;13(1):79. doi: 10.3390/pathogens13010079.
2
Polyamine Metabolism in Parasites: A Promising Therapeutic Target.寄生虫中的多胺代谢:有前途的治疗靶点。
Med Sci (Basel). 2022 Apr 22;10(2):24. doi: 10.3390/medsci10020024.
3
A dual regulatory circuit consisting of S-adenosylmethionine decarboxylase protein and its reaction product controls expression of the paralogous activator prozyme in Trypanosoma brucei.一个由 S-腺苷甲硫氨酸脱羧酶蛋白及其反应产物组成的双调控回路控制着在布氏锥虫中同工酶激活剂的表达。
PLoS Pathog. 2018 Oct 26;14(10):e1007404. doi: 10.1371/journal.ppat.1007404. eCollection 2018 Oct.
4
Polyamines in protozoan pathogens.原虫病原体中的多胺。
J Biol Chem. 2018 Nov 30;293(48):18746-18756. doi: 10.1074/jbc.TM118.003342. Epub 2018 Oct 17.

本文引用的文献

1
Identification of Trypanosoma brucei AdoMetDC Inhibitors Using a High-Throughput Mass Spectrometry-Based Assay.使用基于高通量质谱的检测方法鉴定布氏锥虫腺苷甲硫氨酸脱羧酶抑制剂
ACS Infect Dis. 2017 Jul 14;3(7):512-526. doi: 10.1021/acsinfecdis.7b00022. Epub 2017 Apr 7.
2
Improved Synthesis of MDL 73811 - a Potent AdoMetDC Inhibitor and Anti-Trypanosomal Compound.MDL 73811的改进合成——一种强效腺苷甲硫氨酸脱羧酶抑制剂和抗锥虫化合物
Synthesis (Stuttg). 2016 Jul;48(13):2065-2068. doi: 10.1055/s-0035-1561608.
3
Tolerance to Trypanosomatids: A Threat, or a Key for Disease Elimination?对锥虫的耐受性:一种威胁,还是疾病消除的关键?
Trends Parasitol. 2016 Feb;32(2):157-168. doi: 10.1016/j.pt.2015.11.001. Epub 2015 Nov 28.
4
GMP synthase is essential for viability and infectivity of Trypanosoma brucei despite a redundant purine salvage pathway.尽管存在冗余的嘌呤补救途径,但GMP合酶对于布氏锥虫的生存能力和感染性至关重要。
Mol Microbiol. 2015 Sep;97(5):1006-20. doi: 10.1111/mmi.13083. Epub 2015 Jul 4.
5
The hypusine-containing translation factor eIF5A.含hypusine的翻译因子eIF5A
Crit Rev Biochem Mol Biol. 2014 Sep-Oct;49(5):413-25. doi: 10.3109/10409238.2014.939608. Epub 2014 Jul 17.
6
Trypanosoma brucei S-adenosylmethionine decarboxylase N terminus is essential for allosteric activation by the regulatory subunit prozyme.布氏锥虫 S-腺苷甲硫氨酸脱羧酶 N 端对于调节亚基前酶的别构激活是必需的。
J Biol Chem. 2013 Feb 15;288(7):5232-40. doi: 10.1074/jbc.M112.442475. Epub 2013 Jan 3.
7
Clinical features, diagnosis, and treatment of human African trypanosomiasis (sleeping sickness).人体非洲锥虫病(昏睡病)的临床特征、诊断和治疗。
Lancet Neurol. 2013 Feb;12(2):186-94. doi: 10.1016/S1474-4422(12)70296-X. Epub 2012 Dec 21.
8
Trimethyl lock: A trigger for molecular release in chemistry, biology, and pharmacology.三甲基锁:化学、生物学和药理学中分子释放的触发因素。
Chem Sci. 2012 Jan 1;3(8):2412-2420. doi: 10.1039/C2SC20536J. Epub 2012 May 30.
9
Nifurtimox-eflornithine combination therapy for second-stage gambiense human African trypanosomiasis: Médecins Sans Frontières experience in the Democratic Republic of the Congo.硝呋替莫-依氟鸟氨酸联合疗法治疗第二阶段冈比亚锥虫病:无国界医生组织在刚果民主共和国的经验。
Clin Infect Dis. 2013 Jan;56(2):195-203. doi: 10.1093/cid/cis886. Epub 2012 Oct 16.
10
Untreated human infections by Trypanosoma brucei gambiense are not 100% fatal.未经治疗的冈比亚锥虫人体感染并非 100%致命。
PLoS Negl Trop Dis. 2012;6(6):e1691. doi: 10.1371/journal.pntd.0001691. Epub 2012 Jun 12.

5'-(((Z)-4-氨基-2-丁烯基)甲基氨基)-5'-脱氧腺苷(MDL 73811,或AbeAdo)类似物的合成与评价——一种具有抗锥虫活性的S-腺苷甲硫氨酸脱羧酶抑制剂

Synthesis and evaluation of analogs of 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (MDL 73811, or AbeAdo) - An inhibitor of S-adenosylmethionine decarboxylase with antitrypanosomal activity.

作者信息

Brockway Anthony J, Volkov Oleg A, Cosner Casey C, MacMillan Karen S, Wring Stephen A, Richardson Thomas E, Peel Michael, Phillips Margaret A, De Brabander Jef K

机构信息

Department of Biochemistry, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9038, USA.

Department of Pharmacology, University of Texas Southwestern Medical Center, 6001 Forest Park Rd., Dallas, TX 75390-9041, USA.

出版信息

Bioorg Med Chem. 2017 Oct 15;25(20):5433-5440. doi: 10.1016/j.bmc.2017.07.063. Epub 2017 Aug 3.

DOI:10.1016/j.bmc.2017.07.063
PMID:28807574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5632197/
Abstract

We describe our efforts to improve the pharmacokinetic properties of a mechanism-based suicide inhibitor of the polyamine biosynthetic enzyme S-adenosylmethionine decarboxylase (AdoMetDC), essential for the survival of the eukaryotic parasite Trypanosoma brucei responsible for Human African Trypanosomiasis (HAT). The lead compound, 5'-(((Z)-4-amino-2-butenyl)methylamino)-5'-deoxyadenosine (1, also known as MDL 73811, or AbeAdo), has curative efficacy at a low dosage in a hemolymphatic model of HAT but displayed no demonstrable effect in a mouse model of the CNS stage of HAT due to poor blood-brain barrier permeation. Therefore, we prepared and evaluated an extensive set of analogs with modifications in the aminobutenyl side chain, the 5'-amine, the ribose, and the purine fragments. Although we gained valuable structure-activity insights from this comprehensive dataset, we did not gain traction on improving the prospects for CNS penetration while retaining the potent antiparasitic activity and metabolic stability of the lead compound 1.

摘要

我们描述了为改善一种基于机制的自杀性抑制剂的药代动力学特性所做的努力,该抑制剂作用于多胺生物合成酶S-腺苷甲硫氨酸脱羧酶(AdoMetDC),对于导致人类非洲锥虫病(HAT)的真核寄生虫布氏锥虫的存活至关重要。先导化合物5'-(((Z)-4-氨基-2-丁烯基)甲基氨基)-5'-脱氧腺苷(1,也称为MDL 73811或AbeAdo)在HAT的血淋巴模型中低剂量时具有治愈效果,但由于血脑屏障通透性差,在HAT中枢神经系统阶段的小鼠模型中未显示出明显效果。因此,我们制备并评估了一系列在氨基丁烯基侧链、5'-胺、核糖和嘌呤片段上有修饰的类似物。尽管我们从这个全面的数据集中获得了有价值的构效关系见解,但在保留先导化合物1的强效抗寄生虫活性和代谢稳定性的同时,我们未能在改善中枢神经系统渗透前景方面取得进展。