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Synthesis, antimicrobial, and mitotic toxicity evaluation of new 6‐substituted 2‐(benzo[4,5]imidazo[1,2‐c]quinazolin‐5(6H)‐yl)acetic acids
Journal of Heterocyclic Chemistry ( IF 2.0 ) Pub Date : 2020-09-29 , DOI: 10.1002/jhet.4161
Dmytro V. Kravtsov 1 , Oleksii Yu Voskoboinik 1 , Serhii I. Kovalenko 1
Affiliation  

A series of novel 6‐substituted 2‐(benzo[4,5]imidazo[1,2‐c]quinazolin‐5(6H)‐yl)acetic acids were synthesized and characterized by 1H, 13C, 19F NMR, 1H‐1H‐COSY, 1H‐13C‐HSQC, NOESY, LC‐MS, IR, and elemental analysis. The mitotic toxicity of the synthesized compounds was determined according to the Allium test procedure. The 2‐(6‐(pentafluorophenyl)benzo[4,5]imidazo[1,2‐c]quinazolin‐5(6H)‐yl)acetic acid inhibited mitotic spindle formation, which resulted in significant cytotoxic effect for meristematic cells of Allium cepa l. roots. In a preliminary antimicrobial evaluation, only Streptococcus pyogenes and Candida albicans were slightly susceptible to some of the synthesized compounds.

中文翻译:

新型6-取代的2-(苯并[4,5]咪唑并[1,2-c]喹唑啉-5(6H)-基)乙酸的合成,抗菌和有丝分裂毒性评估

合成了一系列新颖的6-取代的2-(苯并[4,5]咪唑并[1,2 - c ]喹唑啉-5(6 H)-基)乙酸,并通过1 H,13 C,19 F NMR表征,1 H- 1 H-COSY,1 H- 13 C-HSQC,NOESY,LC-MS,IR和元素分析。根据葱属测试方法确定合成化合物的有丝分裂毒性。2-(6-(五氟苯基)苯并[4,5]咪唑并[1,2 - c ]喹唑啉-5(6 H)-基)乙酸抑制有丝分裂纺锤体的形成,对分生组织细胞产生明显的细胞毒性作用洋葱 。根。在初步的抗菌评估中,只有化脓性链球菌白色念珠菌对某些合成化合物略有敏感性。
更新日期:2020-09-29
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