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SOME ASPECTS OF THE MARKETING STUDIES FOR THE PHARMACEUTICAL MARKET OF ANTIVIRAL DRUGS 针对医药市场抗病毒药物的市场营销研究的一些方面
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2015-01-01 DOI: 10.19163/2307-9266-2015-3-6(13)-60-63
A. Salnikova, E. G. Balakhonova
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引用次数: 0
NATURAL POLYACETYLENE COMPOUNDS 天然聚乙炔化合物
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2015-01-01 DOI: 10.19163/2307-9266-2014-2-4(5)-23-47
D. Konovalov
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引用次数: 6
МОЛЕКУЛЯРНЫЙ ДОКИНГ N-ЗАМЕЩЕННОГО ПРОИЗВОДНОГО ИЗОХИНОЛОНАС КАТАЛИТИЧЕСКИМ ДОМЕНОМ ПРОТЕИНКИНАЗЫ C 蛋白激酶C催化结构域对异醌酮N代衍生物的分子修饰
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2014-01-01 DOI: 10.19163/2307-9266-2014-2-1(2)-3-7
А. А. Глушко, Андрей Владиславович Воронков, Иван Панайотович Кодониди, А. В. Бичеров, Михаил Васильевич Черников
Endothelium, representing panacrine gland, regulates a whole range of vitally important functions of organism. The disorder of its work - endothelial dysfunction is a key link of development of cardio-vascular diseases. Considering that this group of pathology relates to the most social significant diseases, the correction of endothelial dysfunction and the search of substances with endothelial tread activity, become an actual task for not only the pharmacology but for adjacent interrelated disciplines such as medicinal chemistry. The significant factor in pathogenesis of endothelial dysfunction development is the reduction of activity of endothelial No-synthase enzyme. One of the possible mechanism of reduction of e NOS activity at the pathology is phosphorylation by protein kinase C(PKC). Due to this fact the site of connection of No synthase enzyme by protein kinase is one of perspective method of molecular docking and can be used for search of substances with endothelial-tread activity. The forecast of biological activity of N-substituted derivative of isoquinolone was done with using a molecular docking method. The obtained results give the opportunity to presume the presence of the endothelial-tread activity of this compound.
内皮细胞是胰腺腺的代表,调控着机体的一系列至关重要的功能。其功能紊乱——内皮功能障碍是心血管疾病发生发展的关键环节。考虑到这组病理与最具社会意义的疾病有关,内皮功能障碍的纠正和内皮层活性物质的寻找不仅成为药理学的实际任务,而且成为邻近相关学科(如药物化学)的实际任务。内皮无合酶活性降低是内皮功能障碍发生的重要因素。病理上enos活性降低的可能机制之一是蛋白激酶C(PKC)磷酸化。因此,蛋白激酶与No合成酶的连接位点是分子对接的一种有前景的方法,可用于寻找具有内皮层活性的物质。采用分子对接法对异喹诺酮n取代衍生物的生物活性进行了预测。所获得的结果使我们有机会假设该化合物的内皮层活性的存在。
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引用次数: 2
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Pharmacy & Pharmacology-Farmatsiya i Farmakologiya
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