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本文引用的文献

1
Synthesis, Immunosuppressive Properties, and Mechanism of Action of a New Isoxazole Derivative.新型异恶唑衍生物的合成、免疫抑制特性及作用机制。
Molecules. 2018 Jun 26;23(7):1545. doi: 10.3390/molecules23071545.
2
The recent progress of isoxazole in medicinal chemistry.异恶唑在药物化学中的最新进展。
Bioorg Med Chem. 2018 Jul 23;26(12):3065-3075. doi: 10.1016/j.bmc.2018.05.013. Epub 2018 May 28.
3
Indolyl-isoxazolidines attenuate LPS-stimulated pro-inflammatory cytokines and increase survival in a mouse model of sepsis: Identification of potent lead.吲哚异恶唑烷类化合物可减轻 LPS 刺激的促炎细胞因子并提高脓毒症小鼠模型的存活率:有效先导化合物的鉴定。
Eur J Med Chem. 2018 Jun 10;153:56-64. doi: 10.1016/j.ejmech.2018.04.004. Epub 2018 Apr 3.
4
SYNTHESIS AND IMMUNOREGULATORY PROPERTIES OF SELECTED 5-AMINO-3-METHYL-4-ISOXAZOLECARBOXYLIC ACID BENZYLAMIDES.某些5-氨基-3-甲基-4-异恶唑羧酸苄基酰胺的合成及免疫调节特性
Acta Pol Pharm. 2016 Sep;73(5):1201-1211.
5
The safety profile of parecoxib for the treatment of postoperative pain: a pooled analysis of 28 randomized, double-blind, placebo-controlled clinical trials and a review of over 10 years of postauthorization data.帕瑞昔布用于治疗术后疼痛的安全性分析:28项随机、双盲、安慰剂对照临床试验的汇总分析及10余年上市后数据回顾
J Pain Res. 2017 Oct 10;10:2451-2459. doi: 10.2147/JPR.S136052. eCollection 2017.
6
Isoxazole ring as a useful scaffold in a search for new therapeutic agents.异恶唑环作为一种有用的骨架,用于寻找新的治疗剂。
Eur J Med Chem. 2017 Sep 8;137:292-309. doi: 10.1016/j.ejmech.2017.06.002. Epub 2017 Jun 2.
7
Synthesis, anti-inflammatory, cyclooxygenases inhibitions assays and histopathological study of poly-substituted 1,3,5-triazines: Confirmation of regiospecific pyrazole cyclization by HMBC.多取代1,3,5-三嗪的合成、抗炎、环氧化酶抑制测定及组织病理学研究:通过HMBC对区域特异性吡唑环化的确认
Eur J Med Chem. 2017 Feb 15;127:10-21. doi: 10.1016/j.ejmech.2016.12.030. Epub 2016 Dec 23.
8
Immunoregulatory effects of 4-(4-chlorophenyl)-1-(5-amino-3-methylisoxazole-4-carbonyl)-thiosemicarbazide (06K) in non-immunized and SRBC-immunized mice.4-(4-氯苯基)-1-(5-氨基-3-甲基异恶唑-4-羰基)-氨基硫脲(06K)对未免疫和经绵羊红细胞免疫小鼠的免疫调节作用
J Pharm Pharmacol. 2016 Dec;68(12):1613-1620. doi: 10.1111/jphp.12631. Epub 2016 Oct 26.
9
5-Amino-3-methyl-4-isoxazolecarboxylic acid hydrazide derivatives with in vitro immunomodulatory activities.具有体外免疫调节活性的5-氨基-3-甲基-4-异恶唑甲酰肼衍生物。
Chem Biol Drug Des. 2017 May;89(5):705-713. doi: 10.1111/cbdd.12892. Epub 2016 Nov 24.
10
Influence of 5-amino-3-methyl-4-isoxazolecarbohydrazide on selective gene expression in Caco-2 cultured cells.5-氨基-3-甲基-4-异恶唑甲酰肼对Caco-2培养细胞中选择性基因表达的影响。
Immunopharmacol Immunotoxicol. 2016 Dec;38(6):486-494. doi: 10.1080/08923973.2016.1247854.

异恶唑衍生物作为免疫功能调节剂。

Isoxazole Derivatives as Regulators of Immune Functions.

机构信息

Laboratory of Immunobiology, Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla 12, 53-114 Wroclaw, Poland.

Department of Organic Chemistry, Faculty of Pharmacy, Wroclaw Medical University, Borowska 211a, 50-556 Wroclaw, Poland.

出版信息

Molecules. 2018 Oct 22;23(10):2724. doi: 10.3390/molecules23102724.

DOI:10.3390/molecules23102724
PMID:30360408
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6222914/
Abstract

In this review, we present reports on the immunoregulatory properties of isoxazole derivatives classified into several categories, such as immunosuppressive, anti-inflammatory, immunoregulatory, and immunostimulatory compounds. The compounds were tested in various models using resident cells from rodents and humans, cell lines, and experimental animal disease models corresponding to human clinical situations. Beneficial features of the described isoxazole derivatives include low toxicity and good bioactivity at low doses. In a majority of studies, the activities of investigated compounds were comparable or even higher than registered reference drugs. Whenever possible, a plausible mechanism of action of the investigated compounds and their potential therapeutic utility were proposed. Among the described compounds, particular attention was paid to the class of immune stimulators with a potential application in chemotherapy patients.

摘要

在这篇综述中,我们报告了几类异恶唑衍生物的免疫调节特性,如免疫抑制、抗炎、免疫调节和免疫刺激化合物。这些化合物在各种模型中进行了测试,使用了来自啮齿动物和人类的常驻细胞、细胞系以及对应于人类临床情况的实验动物疾病模型。所描述的异恶唑衍生物的有益特征包括低毒性和低剂量下的良好生物活性。在大多数研究中,所研究化合物的活性与已注册的参考药物相当或更高。只要有可能,我们就提出了所研究化合物的作用机制及其潜在的治疗用途的合理假设。在所描述的化合物中,特别关注了一类具有在化疗患者中应用潜力的免疫刺激剂。