首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Applying pattern recognition methods and structure property correlations to determine drug carrier potential of nicotinic acid and analogize to dihydropyridine.
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Applying pattern recognition methods and structure property correlations to determine drug carrier potential of nicotinic acid and analogize to dihydropyridine.

机译:应用模式识别方法和结构性质相关性确定烟酸的载药潜力,并与二氢吡啶类似。

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Multivariate methods are utilized to compare nicotinic acid and dihydropyridine as a drug carrier. Nicotinic acid and dihydropyridine form ester groups on 10 beta-lactam antibiotics with an oxymethyl group forming a linkage between the antibiotic and the drug carrier (nicotinic acid or dihydropyridine). Calculated molecular properties are analyzed by self-organizing tree algorithm (SOTA), bivariate regression, cluster analysis, factor analysis, discriminant analysis, hierarchical classification, and principal coordinates analysis. Ten important pharmacological properties for each of the nicotinic acid and dihydropyridine antibiotic derivatives are numerically similar and highly correlated. Calculated molecular properties include molar refractivity, molar volume, parachor, index of refraction, partition coefficient (log P), polarizability, and polar surface area. Dermal permeability coefficients (Kp) for nicotinic acid derivatives are similar to values for dihydropyridine derivatives. Dermal permeabliity coefficients analyzed by hierarchical classification and SOTA analysis were shown to be closely interrelated and highly correlated. Ten properties of the nicotinic acid and dihydropyridine were compared by Passing-Bablok regression analysis and shown to be highly correlated (r=0.9879). Box plot analysis of 10 properties, inclusive of both groups of derivatives, showed narrow ranges in values. Cluster analysis of derivative properties showed the nicotinic acid derivatives to be highly similar to the dihydropyridine derivatives of the same antibiotics. Cluster analysis was performed by single linkage, complete linkage, and centroid linkage. Factor analysis showed the nicotinic acid derivatives to be interrelated and similar to the dihydropyridine derivatives. Discriminant analysis performed on all derivatives formed a single highly cohesive and non-differentiated cluster, demonstrating strong similarity among nicotinic acid and dihydropyridine derivatives. Principal coordinates analysis (determinessimilarity) of Kp values showed high similarity between the nicotinic acid and dihydropyridine antibiotic derivatives.
机译:利用多变量方法比较烟酸和二氢吡啶作为药物载体。烟酸和二氢吡啶在10种β-内酰胺类抗生素上形成酯基,而氧甲基在抗生素和药物载体(烟酸或二氢吡啶)之间形成连接。通过自组织树算法(SOTA),双变量回归,聚类分析,因子分析,判别分析,层次分类和主坐标分析来分析计算的分子特性。烟酸和二氢吡啶类抗生素衍生物各自的十个重要药理特性在数值上相似且高度相关。计算的分子性质包括摩尔折射率,摩尔体积,降落伞,折射率,分配系数(log P),极化率和极性表面积。烟酸衍生物的皮肤渗透系数(Kp)与二氢吡啶衍生物的值相似。通过分层分类和SOTA分析分析的皮肤通透性系数显示密切相关且高度相关。通过Passing-Bablok回归分析比较了烟酸和二氢吡啶的十种性质,并显示出高度相关性(r = 0.9879)。包括两组衍生物在内的10种特性的箱形图分析显示,值的范围很窄。衍生物特性的聚类分析表明,烟酸衍生物与相同抗生素的二氢吡啶衍生物高度相似。聚类分析通过单连锁,完全连锁和质心连锁进行。因子分析表明,烟酸衍生物相互关联且与二氢吡啶衍生物相似。对所有衍生物进行的判别分析形成了一个高内聚力且未分化的簇,这表明烟酸和二氢吡啶衍生物之间具有很强的相似性。 Kp值的主坐标分析(确定相似性)显示,烟酸和二氢吡啶类抗生素衍生物之间具有高度相似性。

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