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首页> 外文期刊>Iranian Journal of Chemistry and Chemical Engineering >Interaction of Bioactive Pyrazolo[4,3-a]acridines with Human Serum Albumin
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Interaction of Bioactive Pyrazolo[4,3-a]acridines with Human Serum Albumin

机译:生物活性吡唑并[4,3-a] ac啶与人血清白蛋白的相互作用

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摘要

Several heterocyclic bioactive fluorescent 3-alkyl-3H-pyrazolo[4,3-a]acriding-11-carbonitriles were conveniently synthesized from the reaction of 1-alkyl-1H-indazoles with different aryl acetonitrile in basic methanol solution in good yields. The interactions of 3H-pyrazolo[4,3-a]acridin-11-carbonitriles with Human Serum Albumin (HSA) were studied by fluorescence spectroscopy. The binding of 3-alkyl-3H-pyrazolo[4,3-a]acridin-11-carbonitriles quenches the HSA fluorescence, revealing a 1:1 interaction with a binding constant of about 1.28 x 10(3) - 1.85 x 10(3) M-1. A decrease in fluorescence intensity at 339 nm, when excited at 295 nm, is attributed to changes in the environment of the protein fluorophores caused by the presence of the ligand. The results show that pyrazolo[4,3-a]acridines with R=propyl, butyl, isobutyl and R'=chlorine substituents have suitable thermodynamic and binding parameters with HSA.
机译:在碱性甲醇溶液中,由1-烷基-1H-吲唑与不同的芳基乙腈反应,可方便地合成几种杂环生物活性荧光3-烷基-3H-吡唑并[4,3-a] ac杂-11-腈。用荧光光谱法研究了3H-吡唑并[4,3-a] ac啶11腈与人血清白蛋白(HSA)的相互作用。 3-烷基-3H-吡唑并[4,3-a] ac啶酮-11腈的结合淬灭了HSA荧光,揭示了1:1相互作用,结合常数约为1.28 x 10(3)-1.85 x 10( 3)M-1。当在295 nm激发时,339 nm的荧光强度降低归因于配体的存在引起的蛋白质荧光团环境的变化。结果表明,具有R =丙基,丁基,异丁基和R′=氯取代基的吡唑并[4,3-a] ac啶具有合适的热力学和与HSA的结合参数。

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