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关于磁流变弹性体的工业应用:药物发现和仿制药合成中的分子多样性。

On the industrial applications of MCRs: molecular diversity in drug discovery and generic drug synthesis.

机构信息

Priaxon AG, Gmunder Straße 37-37a, 81379, Munich, Germany.

出版信息

Mol Divers. 2010 Aug;14(3):513-22. doi: 10.1007/s11030-010-9225-x. Epub 2010 Mar 16.

DOI:10.1007/s11030-010-9225-x
PMID:20229364
Abstract

During the last decades, multicomponent chemistry has gained much attention in pharmaceutical research, especially in the context of lead finding and optimization. Here, in particular, the main advantages of multicomponent reactions (MCRs) like ease of automation and high diversity generation were utilized. In consequence of these beneficial properties, a plethora of new MCRs combined with appropriate classical reaction sequences have been published, the accessible chemical space was extended steadily. In the meantime, the desired high diversity became a challenge itself, because by now the systematic use of this huge and unmanageable space for drug discovery was limited by the lack of suitable computational tools. Therefore, this article provides an insight for the rational use of this enormous chemical space in drug discovery and generic drug synthesis. In this context, a short overview of the applied chemo informatics, necessary for the virtual screening of the biggest available chemical space, is given. Furthermore, some examples for recently developed multicomponent sequences are presented.

摘要

在过去的几十年中,多组分化学在药物研究中受到了广泛关注,特别是在寻找和优化先导化合物方面。特别是,多组分反应(MCRs)的主要优点,如易于自动化和高多样性的产生,得到了利用。由于这些有益的特性,大量新的多组分反应与适当的经典反应序列相结合已经被发表,可及的化学空间不断扩展。同时,所需的高多样性本身也成为了一个挑战,因为到目前为止,由于缺乏合适的计算工具,系统地利用这个庞大且难以管理的空间进行药物发现受到了限制。因此,本文提供了一种合理利用这一巨大化学空间进行药物发现和仿制药合成的方法。在这方面,简要概述了应用于虚拟筛选最大可用化学空间所需的化学信息学。此外,还介绍了一些最近开发的多组分序列的例子。

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本文引用的文献

1
Patented small molecule inhibitors of p53-MDM2 interaction.专利的 p53-MDM2 相互作用小分子抑制剂。
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2
Emerging molecular diversity from the intra-molecular Ugi reaction: iterative efficiency in medicinal chemistry.分子内Ugi反应产生的新分子多样性:药物化学中的迭代效率
Mol Divers. 2009 May;13(2):195-207. doi: 10.1007/s11030-009-9111-6. Epub 2009 Feb 11.
3
Isoquinolin-1-one inhibitors of the MDM2-p53 interaction.MDM2-p53相互作用的异喹啉-1-酮抑制剂。
Pharmaceuticals (Basel). 2022 Aug 17;15(8):1009. doi: 10.3390/ph15081009.
4
An efficient and green synthesis of ferrocenyl-quinoline conjugates a TsOH-catalyzed three-component reaction in water.一种高效绿色的二茂铁基喹啉共轭物的合成——水相中对甲苯磺酸催化的三组分反应。
RSC Adv. 2018 Mar 6;8(17):9555-9563. doi: 10.1039/c8ra01004h. eCollection 2018 Feb 28.
5
MCR Scaffolds Get Hotter with F-Labeling.MCR 支架通过 F 标记变得更热。
Molecules. 2019 Apr 4;24(7):1327. doi: 10.3390/molecules24071327.
6
Synergy Effects in the Chemical Synthesis and Extensions of Multicomponent Reactions (MCRs)-The Low Energy Way to Ultra-Short Syntheses of Tailor-Made Molecules.多组分反应(MCRs)化学合成与拓展中的协同效应——定制分子超短合成的低能途径
Molecules. 2017 Feb 25;22(3):349. doi: 10.3390/molecules22030349.
7
Applications of Palladium-Catalyzed C-N Cross-Coupling Reactions.钯催化的碳-氮交叉偶联反应的应用
Chem Rev. 2016 Oct 12;116(19):12564-12649. doi: 10.1021/acs.chemrev.6b00512. Epub 2016 Sep 30.
8
Synthesis of isoindolin-1-one derivatives via multicomponent reactions of methyl 2-formylbenzoate and intramolecular amidation.通过2-甲酰基苯甲酸甲酯的多组分反应和分子内酰胺化合成异吲哚啉-1-酮衍生物。
Mol Divers. 2016 Nov;20(4):859-865. doi: 10.1007/s11030-016-9679-6. Epub 2016 Jun 7.
9
An Expedient Regio- and Diastereoselective Synthesis of Hybrid Frameworks with Embedded Spiro[9,10]dihydroanthracene [9,3']-pyrrolidine and Spiro[oxindole-3,2'-pyrrolidine] Motifs via an Ionic Liquid-Mediated Multicomponent Reaction.通过离子液体介导的多组分反应,便捷地区域和非对映选择性合成具有嵌入螺[9,10]二氢蒽[9,3']-吡咯烷和螺[氧化吲哚-3,2'-吡咯烷]基序的杂化骨架。
Molecules. 2015 Sep 3;20(9):16142-53. doi: 10.3390/molecules200916142.
10
Expanding the substrate scope of Ugi five-center, four-component reaction U-5C-4CR): ketones as coupling partners for secondary amino acids.拓展 Ugi 五组分反应 U-5C-4CR 的底物范围:酮作为仲胺的偶联伙伴。
Mol Divers. 2014 Feb;18(1):61-77. doi: 10.1007/s11030-013-9488-0. Epub 2013 Oct 24.
ChemMedChem. 2008 Jul;3(7):1118-28. doi: 10.1002/cmdc.200800025.
4
Activity of androgen receptor antagonist bicalutamide in prostate cancer cells is independent of NCoR and SMRT corepressors.雄激素受体拮抗剂比卡鲁胺在前列腺癌细胞中的活性独立于NCoR和SMRT共抑制因子。
Cancer Res. 2007 Sep 1;67(17):8388-95. doi: 10.1158/0008-5472.CAN-07-0617.
5
Multicomponent synthesis of dihydrobenzoxazepinones by coupling Ugi and Mitsunobu reactions.通过乌吉反应和光延反应的偶联实现二氢苯并恶唑嗪酮的多组分合成。
Org Biomol Chem. 2006 Nov 21;4(22):4236-40. doi: 10.1039/b613056a.
6
LIGSITEcsc: predicting ligand binding sites using the Connolly surface and degree of conservation.LIGSITEcsc:利用康诺利表面和保守程度预测配体结合位点。
BMC Struct Biol. 2006 Sep 24;6:19. doi: 10.1186/1472-6807-6-19.
7
Rapid access to oxindoles by the combined use of an Ugi four-component reaction and a microwave-assisted intramolecular Buchwald-Hartwig amidation reaction.通过联合使用乌吉四组分反应和微波辅助分子内布赫瓦尔德-哈特维希酰胺化反应快速合成氧化吲哚。
Org Lett. 2006 Sep 14;8(19):4351-4. doi: 10.1021/ol061755z.
8
Parallel synthesis of a library of benzoxazoles and benzothiazoles using ligand-accelerated copper-catalyzed cyclizations of ortho-halobenzanilides.利用配体加速的邻卤代苯甲酰苯胺的铜催化环化反应平行合成苯并恶唑和苯并噻唑文库。
J Org Chem. 2006 Mar 3;71(5):1802-8. doi: 10.1021/jo051927q.
9
Recent developments in isocyanide based multicomponent reactions in applied chemistry.应用化学中基于异腈的多组分反应的最新进展。
Chem Rev. 2006 Jan;106(1):17-89. doi: 10.1021/cr0505728.
10
Three-component synthesis of polysubstituted 6-azaindolines and its tricyclic derivatives.多取代6-氮杂吲哚啉及其三环衍生物的三组分合成
Org Lett. 2005 Jan 20;7(2):239-42. doi: 10.1021/ol0477881.