Pleiotropic focused anticancer approach by dihydropyridines, dihydropyrimidines and heteroaromatic compounds

G. Duburs, B. Vigante, E. Bisenieks, A. Krauze, A. Plotniece, A. Sobolev, I. Domracheva, K. Pajuste
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引用次数: 2

Abstract

Complex, focused anticancer therapy approach has been developed in the Latvian Institute of Organic Synthesis by making use of privileged partially hydrogenated nitrogen-containing heterocycles, namely dihydropyridines, dihydropyrimidines, their oxidized heteroaromatic derivatives. Topics of research include: 1. Conventional approach by chemotherapy and synergism of anticancer drugs [1]; 2. Inhibition of multidrug resistance by inhibition of drug efflux pumps [2]; 3. Mitigation of cancer risk factors – e.g., hepatitis B virus chemotherapy for prevention of chronic liver diseases, because chronic hepatitis, in up to 40% of cases, progresses to cyrrhosis and further to hepatocellular carcinoma [3]; 4. Improvement of efficacy of cancer radiotherapy by use of radioprotectors to prevent damage of normal tissues. So, radioprotector diethone (dietone) for skin protection was discovered, elaborated, and developed as ointment. Compounds for protection of eyes, mucous tissues, salivary glands etc have been synthesized. Toxicity of dietone and novel radioprotectors is very low; 5.Amphiphilic compounds have been synthesized, nanoparticles for anticancer drug and gene delivery have been created, pleiotropic properties have been checked, inclusion of magnetic particles for targeted transport performed [4]. Acknowledgements The research was partially supported by the Latvian State Program Biomedicine. References 1.Bisenieks E., Duburs G. et al., Pharmaceutical combination of 5-fluorouracil and derivatives of 1,4-dihydropyridine. US 8492413B2, 2013. 2.Krauze A., Grinberga S. et al., Thieno[2,3-b]pyridines – a new class of multidrug resistance (MDR) modulators. Bioorg.Med.Chem. 2014, 22 (21), 5860-5870. 3.Sipola A., Dubova U., et al., Synthesis and evaluation of 1,4-dihydropyrimidine derivatives – hepatitis B virus capsid self-assembly inhibitors. EFMC International Symposium on Medicinal Chemistry. Ljubljana, Slovenia, 2018, P176. 4.Pajuste K. et al., Gene delivery agents possessing antiradical activity: Self-assembling cationic amphiphilic 1,4-dihydropyridine derivatives. New J.Chem. 2013, 37 (10), 3062-3075.
二氢吡啶、二氢嘧啶和杂芳香化合物的多效聚焦抗癌方法
拉脱维亚有机合成研究所通过利用特殊的部分氢化含氮杂环,即二氢吡啶、二氢嘧啶及其氧化的杂芳香衍生物,开发了复杂、集中的抗癌治疗方法。研究课题包括:1。2.常规途径的化疗与抗癌药物的协同作用[1];2 .抑制药物外排泵抑制多药耐药[2];3 .减轻癌症危险因素——例如,通过乙型肝炎病毒化疗预防慢性肝病,因为多达40%的慢性肝炎病例会发展为肝硬化并进一步发展为肝细胞癌[3];利用放射防护剂防止正常组织损伤,提高癌症放射治疗的疗效。因此,用于皮肤防护的放射性保护剂二乙酮(dietone)被发现、加工并制成软膏。已经合成了保护眼睛、粘膜组织、唾液腺等的化合物。4 .二酮和新型放射性防护剂的毒性很低;两亲性化合物已被合成,用于抗癌药物和基因传递的纳米颗粒已被创造,多效性已被检查,磁性颗粒的靶向运输已被执行[4]。本研究得到了拉脱维亚国家生物医学计划的部分支持。Bisenieks E., Duburs G.等,5-氟尿嘧啶和1,4-二氢吡啶衍生物的药物组合。Us 8492413b2, 2013.2。王晓明,王晓明,王晓明,等。一类新型多药耐药(MDR)调节剂的研究进展[j]。Bioorg.Med.Chem。2014, 22(21), 5860-5870.3。王晓明,王晓明,等。1,4-二氢嘧啶衍生物-乙型肝炎病毒衣壳自组装抑制剂的合成与评价。EFMC国际药物化学研讨会。卢布尔雅那,斯洛文尼亚,2018,P176.4。Pajuste K.等,具有抗自由基活性的基因递送剂:自组装阳离子两亲性1,4-二氢吡啶衍生物。新的J.Chem。2013, 37(10), 3062-3075。
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