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细胞因子的定量构效关系研究。综述、评价与比较研究。

Cytokines in terms of QSAR. Review, evaluation and comparative studies.

机构信息

a Department of Pharmaceutical Chemistry , School of Pharmacy, Aristotle University of Thessaloniki , Thessaloniki , Greece .

出版信息

SAR QSAR Environ Res. 2013 Nov;24(11):883-962. doi: 10.1080/1062936X.2013.815656. Epub 2013 Oct 7.

Abstract

Cytokines represent a class of chemical factors that act as mediators in the complex biological response of inflammation, potentially implicated in various diseases. Therefore, selective inhibition or antagonism of cytokines is a target of anti-inflammatory drug design. The QSAR (Quantitative Structure-Activity Relationships) analysis presented here attempts to identify the structural features and physicochemical properties that are significant for cytokine antagonists or inhibitors and in particular of i) interleukin-5 (IL-5), ii) interleukin-6 (IL-6) and iii) of the chemotactic cytokine (chemokine) interleukin-8 (IL-8). Firstly, a historical aspect of the limited published QSARs is discussed and then a 2D-QSAR analysis was carried out for 26 data sets of compounds using the C-QSAR program of Biobyte. In six cases hydrophobicity appeared to be important. Steric factors in the form of overall molar refractivity (CMR), molar refractivity of the substituent (MR), molar volume (MgVol), Taft's Es constant and the sterimol parameters B1 and B5 have a significant impact on biological activity in most of the derived equations whereas electronic parameters as σp, σm or Σσ appeared in five cases.

摘要

细胞因子是一类化学因子,作为炎症复杂生物反应的介质,可能与各种疾病有关。因此,细胞因子的选择性抑制或拮抗作用是抗炎药物设计的目标。这里提出的 QSAR(定量构效关系)分析试图确定对细胞因子拮抗剂或抑制剂具有重要意义的结构特征和物理化学性质,特别是:i)白细胞介素-5(IL-5),ii)白细胞介素-6(IL-6)和 iii)趋化细胞因子(趋化因子)白细胞介素-8(IL-8)。首先,讨论了有限发表的 QSAR 的历史方面,然后使用 Biobyte 的 C-QSAR 程序对 26 个化合物数据集进行了 2D-QSAR 分析。在六种情况下,疏水性似乎很重要。以总摩尔折射度(CMR)、取代基摩尔折射度(MR)、摩尔体积(MgVol)、Taft 的 Es 常数和 sterimol 参数 B1 和 B5 的形式出现的立体因素在大多数衍生方程中对生物活性有重大影响,而电子参数如 σp、σm 或 Σσ 在五种情况下出现。

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