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Azole Based Acetohydrazide Derivatives of Cinnamaldehyde Target and Kill Candida albicans by Causing Cellular Apoptosis

机译:基于淀粉基丙基酰肼衍生物的肉桂醛靶标并通过引起细胞凋亡来杀死念珠菌

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Opportunistic fungal pathogens including Candida albicans are responsible for the alarming rise in hospital acquired infections and millions of deaths worldwide. The current treatment modalities are not enough to handle this situation, and therefore, new treatment modalities and strategies are desperately needed. In this direction, we synthesized a series of azole based acetohydrazide derivatives of cinnamaldehyde and subjected it to antifungal activity evaluation. Preliminary antifungal activity evaluation revealed tremendous antifungal potential of some of the derivatives against fluconazole susceptible and resistant clinical isolates of Candida albicans. Although all the compounds in the series are structurally similar except for the presence of different substituents on the phenyl ring of the acetohydrazide pendent, they sharply differed in their activity profile. Further mechanism of action studies revealed that these compounds have an apoptotic effect on C. albicans confirmed via Annexin V-FITC staining and TUNEL assay.
机译:在内的机会性真菌病原体,包括念珠菌白化人负责医院收购感染和全球数百万死亡的令人震惊的上升。目前的治疗方式不足以处理这种情况,因此,迫切需要新的治疗方式和策略。在这种方向上,我们合成了一系列基于肉桂醛的丙基酰肼衍生物,并使其进行抗真菌活性评估。初步抗真菌活性评价揭示了一些针对氟康唑敏感和抗念珠菌临床分离株的一些衍生物的巨大抗真菌潜力。虽然该系列中的所有化合物在结构上类似,但是除乙酰肼底形的苯环上存在不同的取代基,它们在其活性谱中急剧不同。行动研究的进一步机制揭示了这些化合物对通过膜蛋白V-FITC染色和TUNEL测定的敏感剂进行凋亡作用。

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