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哒嗪酮类似物概述:化学及药理潜力

An Overview of Pyridazinone Analogs: Chemical and Pharmacological Potential.

作者信息

Boukharsa Youness, Karrouchi Khalid, Attjioui Houda, Ansar M'Hammed

机构信息

Laboratory of Medicinal Chemistry, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco.

Higher Institute of Nursing Professions and Technical Health (ISPITS), Casablanca, Morocco.

出版信息

Mini Rev Med Chem. 2025;25(1):3-26. doi: 10.2174/0113895575287746240528072330.

DOI:10.2174/0113895575287746240528072330
PMID:38859779
Abstract

Pyridazinones are classical molecules that occupy an important place in heterocyclic chemistry, and since their discovery, they have been widely developed. The introduction of new functional groups into pyridazinone structures has enabled the synthesis of a large diversity of compounds. The pharmacological and agrochemical importance of pyridazinone derivatives has aroused the interest of chemists and directed their research toward the synthesis of new compounds with the aim of improving their biological effectiveness. In this review, we have compiled and discussed the different synthetic routes, reactivity, and pharmacological and agrochemical applications of the pyridazinone ring.

摘要

哒嗪酮是在杂环化学中占据重要地位的经典分子,自其被发现以来,已得到广泛开发。在哒嗪酮结构中引入新的官能团使得能够合成种类繁多的化合物。哒嗪酮衍生物在药理学和农业化学方面的重要性引起了化学家们的兴趣,并引导他们开展研究以合成新化合物,旨在提高其生物活性。在本综述中,我们汇编并讨论了哒嗪酮环的不同合成路线、反应性以及药理学和农业化学应用。

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本文引用的文献

1
New platelet aggregation inhibitors based on pyridazinone moiety.基于哒嗪酮部分的新型血小板聚集抑制剂。
Eur J Med Chem. 2015 Apr 13;94:113-22. doi: 10.1016/j.ejmech.2015.02.061. Epub 2015 Mar 3.
2
Identification and optimization of pyridazinones as potent and selective c-Met kinase inhibitors.哒嗪酮类作为强效和选择性c-Met激酶抑制剂的鉴定与优化。
Bioorg Med Chem Lett. 2015 Apr 1;25(7):1597-602. doi: 10.1016/j.bmcl.2015.02.002. Epub 2015 Feb 16.
3
Further studies on pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as potent and selective human A1 adenosine receptor antagonists.
关于吡唑并[1',5':1,6]嘧啶并[4,5-d]哒嗪-4(3H)-酮作为强效和选择性人A1腺苷受体拮抗剂的进一步研究。
Eur J Med Chem. 2015 Jan 7;89:32-41. doi: 10.1016/j.ejmech.2014.10.020. Epub 2014 Oct 12.
4
Design, synthesis and structure-activity relationships of novel 4-phenoxyquinoline derivatives containing pyridazinone moiety as potential antitumor agents.新型含哒嗪酮结构的 4-苯氧基喹啉衍生物的设计、合成及构效关系研究作为潜在的抗肿瘤药物。
Eur J Med Chem. 2014 Aug 18;83:581-93. doi: 10.1016/j.ejmech.2014.06.068. Epub 2014 Jun 28.
5
Synthesis of a new class of Pyridazin-3-one and 2-amino-5-arylazopyridine derivatives and their utility in the synthesis of fused azines.一类新型哒嗪-3-酮和2-氨基-5-芳基偶氮吡啶衍生物的合成及其在稠合氮杂环化合物合成中的应用。
Molecules. 2014 Feb 24;19(2):2637-54. doi: 10.3390/molecules19022637.
6
Discovery of (1R,6S)-5-[4-(1-cyclobutyl-piperidin-4-yloxy)-phenyl]-3,4-diaza-bicyclo[4.1.0]hept-4-en-2-one (R,S-4a): histamine H(3) receptor inverse agonist demonstrating potent cognitive enhancing and wake promoting activity.(1R,6S)-5-[4-(1-环丁基-哌啶-4-基氧基)-苯基]-3,4-二氮杂双环[4.1.0]庚-4-烯-2-酮(R,S-4a)的发现:组胺H(3)受体反向激动剂,具有强效认知增强和促觉醒活性。
Bioorg Med Chem Lett. 2014 Mar 1;24(5):1303-6. doi: 10.1016/j.bmcl.2014.01.061. Epub 2014 Jan 30.
7
Approaches towards the synthesis of a novel class of 2-amino-5-arylazonicotinate, pyridazinone and pyrido[2,3-d]pyrimidine derivatives as potent antimicrobial agents.合成一类新型2-氨基-5-芳基偶氮烟酸酯、哒嗪酮和吡啶并[2,3-d]嘧啶衍生物作为强效抗菌剂的方法。
Chem Cent J. 2013 Jul 17;7(1):123. doi: 10.1186/1752-153X-7-123.
8
Randomized crossover study of the histamine H3 inverse agonist MK-0249 for the treatment of cognitive impairment in patients with schizophrenia.随机交叉研究组胺 H3 反向激动剂 MK-0249 治疗精神分裂症患者认知障碍。
Schizophr Res. 2013 May;146(1-3):224-30. doi: 10.1016/j.schres.2013.02.030. Epub 2013 Mar 22.
9
The safety, tolerability, pharmacokinetics and cognitive effects of GSK239512, a selective histamine H₃ receptor antagonist in patients with mild to moderate Alzheimer's disease: a preliminary investigation.在轻度至中度阿尔茨海默病患者中,GSK239512(一种选择性组胺 H₃受体拮抗剂)的安全性、耐受性、药代动力学和认知影响:初步研究。
Curr Alzheimer Res. 2013 Mar;10(3):240-51. doi: 10.2174/1567205011310030003.
10
Synthesis and anti-inflammatory activity of novel pyridazine and pyridazinone derivatives as non-ulcerogenic agents.新型哒嗪和哒嗪酮衍生物的合成及抗炎活性作为非致溃疡剂。
Arch Pharm Res. 2012 Dec;35(12):2077-92. doi: 10.1007/s12272-012-1205-5. Epub 2012 Dec 21.