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构建具有生物活性的多种功能化双环[3.3.1]壬烷的不同途径:抗癌化疗新视角探索

Different routes for the construction of biologically active diversely functionalized bicyclo[3.3.1]nonanes: an exploration of new perspectives for anticancer chemotherapeutics.

作者信息

Roy Nilmadhab, Das Rishav, Paira Rupankar, Paira Priyankar

机构信息

Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology Vellore 632014 Tamilnadu India

Department of Chemistry, Maharaja Manindra Chandra College 20 Ramkanto Bose Street Kolkata 700 003 India

出版信息

RSC Adv. 2023 Jul 25;13(32):22389-22480. doi: 10.1039/d3ra02003g. eCollection 2023 Jul 19.

DOI:10.1039/d3ra02003g
PMID:37501776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10369265/
Abstract

Cancer is the second most high-morbidity disease throughout the world. From ancient days, natural products have been known to possess several biological activities, and research on natural products is one of the most enticing areas where scientists are engrossed in the extraction of valuable compounds from various plants to isolate many life-saving medicines, along with their other applications. It has been noticed that the bicyclo[3.3.1]nonane moiety is predominant in most biologically active natural products owing to its exceptional characteristics compared to others. Many derivatives of bicyclo[3.3.1]nonane are attractive to researchers for use in asymmetric catalysis or as potent anticancer entities along with their successful applications as ion receptors, metallocycles, and molecular tweezers. Therefore, this review article discusses several miscellaneous synthetic routes for the construction of bicyclo[3.3.1]nonanes and their heteroanalogues in association with the delineation of their anticancer activities with few selective compounds.

摘要

癌症是全球第二高发病率的疾病。自古以来,天然产物就被认为具有多种生物活性,对天然产物的研究是最具吸引力的领域之一,科学家们热衷于从各种植物中提取有价值的化合物,以分离出许多救命药物以及它们的其他应用。人们已经注意到,双环[3.3.1]壬烷部分在大多数生物活性天然产物中占主导地位,因为与其他部分相比,它具有特殊的特性。双环[3.3.1]壬烷的许多衍生物因其在不对称催化中的应用、作为有效的抗癌实体以及作为离子受体、金属环和分子镊子的成功应用而吸引了研究人员。因此,这篇综述文章讨论了几种构建双环[3.3.1]壬烷及其杂类似物的各种合成路线,并描述了它们对少数选择性化合物的抗癌活性。

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2
A bio-inspired synthesis of hybrid flavonoids from 2-hydroxychalcone driven by visible light.可见光驱动下由2-羟基查尔酮仿生合成杂合黄酮类化合物。
RSC Adv. 2019 Sep 16;9(50):29005-29009. doi: 10.1039/c9ra07198a. eCollection 2019 Sep 13.
3
Pharmacological Activity of (Kokum): An Updated Review.
刺果番荔枝的药理活性:最新综述
Pharmaceuticals (Basel). 2021 Dec 20;14(12):1338. doi: 10.3390/ph14121338.
4
Garcinol-A Natural Histone Acetyltransferase Inhibitor and New Anti-Cancer Epigenetic Drug.藤黄脂素——一种天然组蛋白乙酰转移酶抑制剂及新型抗癌表观遗传药物。
Int J Mol Sci. 2021 Mar 11;22(6):2828. doi: 10.3390/ijms22062828.
5
Garcinol Is an HDAC11 Inhibitor.姜黄素是一种 HDAC11 抑制剂。
ACS Chem Biol. 2020 Nov 20;15(11):2866-2871. doi: 10.1021/acschembio.0c00719. Epub 2020 Oct 9.
6
Bicyclic polyprenylated acylphloroglucinols and their derivatives: structural modification, structure-activity relationship, biological activity and mechanism of action.双环多异戊烯基酰基间苯三酚及其衍生物:结构修饰、构效关系、生物活性及作用机制
Eur J Med Chem. 2020 Nov 1;205:112646. doi: 10.1016/j.ejmech.2020.112646. Epub 2020 Jul 24.
7
Visible-light driven synthesis of polycyclic benzo[d][1,3]oxazocine from 2-aminochalcone.可见光促进 2-氨基查耳酮合成多环苯并[d][1,3]恶嗪
Chem Commun (Camb). 2020 Jun 18;56(49):6739-6742. doi: 10.1039/d0cc02416c.
8
Garcinol Exhibits Anti-Neoplastic Effects by Targeting Diverse Oncogenic Factors in Tumor Cells.藤黄脂通过靶向肿瘤细胞中的多种致癌因子发挥抗肿瘤作用。
Biomedicines. 2020 Apr 30;8(5):103. doi: 10.3390/biomedicines8050103.
9
The active fraction of Garcinia yunnanensis suppresses the progression of colorectal carcinoma by interfering with tumorassociated macrophage-associated M2 macrophage polarization in vivo and in vitro.云南余甘子的活性部分通过体内和体外干扰与肿瘤相关巨噬细胞相关的 M2 巨噬细胞极化来抑制结直肠癌的进展。
FASEB J. 2020 Jun;34(6):7387-7403. doi: 10.1096/fj.201903011R. Epub 2020 Apr 13.
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The Cuban Propolis Component Nemorosone Inhibits Proliferation and Metastatic Properties of Human Colorectal Cancer Cells.古巴蜂胶成分去甲泽拉木醛抑制人结直肠癌细胞的增殖和转移特性。
Int J Mol Sci. 2020 Mar 6;21(5):1827. doi: 10.3390/ijms21051827.