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新型1,2,4-三唑-3(5)-酮类三唑-硫醇和噻二唑衍生物的合成及生物学性质

Synthesis and biological properties of novel triazole-thiol and thiadiazole derivatives of the 1,2,4-Triazole-3(5)-one class.

作者信息

Düğdü Esra, Unver Yasemin, Unlüer Dilek, Sancak Kemal

机构信息

Department of Chemistry, Karadeniz Technical University, Trabzon 61080, Turkey.

出版信息

Molecules. 2014 Feb 19;19(2):2199-212. doi: 10.3390/molecules19022199.

Abstract

2,2'-(4,4'(Butane-1,4-diyl/hexane-1,6-diyl)bis(3-methyl-5-oxo-4,5-dihydro-1,2,4- triazole-4,1-diyl)) diacetohydrazides 3a,b were obtained via the formation of diethyl 2,2'-(4,4'(butane-1,4-diyl/hexane-1,6-diyl)bis(3-methyl-5-oxo-4,5-dihydro-1,2,4-triazole-4,1- diyl))diacetates 2a,b, obtained starting from di-[3(methyl-2-yl-methyl)-4,5-dihydro-1H-[1,2,4]-triazole-5-one-4yl]-n-alkanes 1a,b in two steps. The synthesis of the compounds 7a,b-9a,b incorporating the 1,3,4-thiadiazole, and 10a,b-11a,b with a 1,2,4-triazole-thiol nucleus as the second heterocycle, was performed by the acidic or basic treatment of compounds 4a,b-6a,b which were obtained from the reaction of 3a,b with several isothiocyanates. Newly synthesized compounds were screened for antimicrobial activities and their antioxidant properties by the 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical scavenging method. Compounds 4a,b, 5a,b, and 6a,b were found to possess good antioxidant properties. Almost all compounds have significant antimicrobial activities.

摘要

2,2'-(4,4'(丁烷-1,4-二基/己烷-1,6-二基)双(3-甲基-5-氧代-4,5-二氢-1,2,4-三唑-4,1-二基))二乙酰肼3a,b是通过两步反应,由二-[3(甲基-2-基-甲基)-4,5-二氢-1H-[1,2,4]-三唑-5-酮-4-基]-正烷烃1a,b起始得到的2,2'-(4,4'(丁烷-1,4-二基/己烷-1,6-二基)双(3-甲基-5-氧代-4,5-二氢-1,2,4-三唑-4,1-二基))二乙酸酯2a,b而制得。通过对3a,b与几种异硫氰酸酯反应得到的化合物4a,b - 6a,b进行酸性或碱性处理,合成了含有1,3,4-噻二唑的化合物7a,b - 9a,b以及含有1,2,4-三唑-硫醇核作为第二个杂环的化合物10a,b - 11a,b。通过1,1-二苯基-2-苦基肼基(DPPH)自由基清除法对新合成的化合物进行了抗菌活性及其抗氧化性能的筛选。发现化合物4a,b、5a,b和6a,b具有良好的抗氧化性能。几乎所有化合物都具有显著的抗菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858c/6271615/bb388eca0fcd/molecules-19-02199-g002.jpg

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