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免疫刺激型CpG寡脱氧核苷酸喹啉拮抗剂的藤田-班QSAR分析及比较分子力场分析研究

Fujita-Ban QSAR analysis and CoMFA study of quinoline antagonists of immunostimulatory CpG-oligodeoxynucleotides.

作者信息

Paliakov Ekaterina, Henary Maged, Say Martial, Patterson Steven E, Parker Alesia, Manzel Lori, Macfarlane Donald E, Bojarski Andrzej J, Strekowski Lucjan

机构信息

Department of Chemistry, Georgia State University, Atlanta, GA 30302, USA.

出版信息

Bioorg Med Chem. 2007 Jan 1;15(1):324-32. doi: 10.1016/j.bmc.2006.09.059. Epub 2006 Sep 29.

Abstract

One hundred seven 2-arylquinolin-4-amines were assayed in vitro for inhibition of the immunostimulatory effect of oligodeoxynucleotides containing a CpG-motif. The compounds are functionalized with various basic and non-basic groups at the aryl moiety and at the amino substituent of the quinolin-4-amine, and some of them contain an additional substituent at position 6 or 7 of the quinoline. Activities of these antagonists, expressed as EC(50) values, range from 0.2 to 200nM. A statistically significant structure-activity correlation was obtained for the Fujita-Ban variant of the classical Free-Wilson analysis. The CoMFA results derived from several models consistently indicate that electrostatic interactions of the molecules with a biological receptor contribute to biological activities to a greater extent than steric effects.

摘要

对107种2-芳基喹啉-4-胺进行了体外试验,以检测其对含CpG基序的寡脱氧核苷酸免疫刺激作用的抑制效果。这些化合物在芳基部分和喹啉-4-胺的氨基取代基上带有各种碱性和非碱性基团进行功能化修饰,其中一些在喹啉的6位或7位含有额外的取代基。这些拮抗剂的活性以EC(50)值表示,范围为0.2至200 nM。通过经典Free-Wilson分析的Fujita-Ban变体获得了具有统计学意义的构效关系。从多个模型得出的CoMFA结果一致表明,分子与生物受体的静电相互作用对生物活性的贡献在程度上大于空间效应。

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