首页> 外文期刊>Archives of pharmacal research >Synthesis and anti-HIV-1 screening of novel N'-(1-(aryl)ethylidene)-2-(5,5-dioxido-3-phenylbenzo[e]pyrazolo[4,3-c][1,2]thiazin-4(1H)-yl)acetohydrazides.
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Synthesis and anti-HIV-1 screening of novel N'-(1-(aryl)ethylidene)-2-(5,5-dioxido-3-phenylbenzo[e]pyrazolo[4,3-c][1,2]thiazin-4(1H)-yl)acetohydrazides.

机译:新型N' - (1-(芳基)乙烯)-2-(5,5-二氧基-3-苯基苯基苯基苯基苯并[e]吡唑[4,3-C] [1,2]的合成和抗HIV-1筛选 噻嗪-4(1H) - 乙基)丙烯酰肼。

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摘要

A novel series of N'-(1-(aryl)ethylidene)-2-(5,5-dioxido-3-phenylbenzo[e]pyrazolo[4,3-c][1,2]thiazin-4(1H)-yl)acetohydrazides was synthesized. The synthesis was carried out by thermal method as well as ultrasonic bath to reduce reaction time and to enhance product yields. The synthesized compounds were characterized by spectroscopic techniques like NMR, infrared and EIMS. The structure of compound 5w was elucidated by X-ray crystallography. The titled compounds were evaluated for anti-human immunodeficiency virus type 1 (anti-HIV-1) and cytotoxic activities. Biological studies indicated that amongst these compounds, 5a, b, j, h and i showed the activity with median effective concentration (EC50) values less than 20 μM. Compound 5i exhibited the most potent anti-HIV-1 activity (EC50 = 3.2 μM) while 5h showed anti-HIV-1 activity (EC50 = 3.8 μM) with no toxicity at all in primary human lymphocytes, CEM and VERO cells.
机译:N' - (1-(芳基)乙基乙烯)-2-(5,5-二氧基-3-苯基苯并[e]吡唑[4,3-C] [1,2]噻嗪-4(1H)的新型系列 - (5,5-二氧化物-3-苯基苯并[1小时) - 丙基酰肼被合成。 通过热法以及超声浴进行合成以减少反应时间并增强产物产率。 合成化合物的特征在于光谱技术,如NMR,红外线和EIMS等光谱技术。 通过X射线晶体学阐明化合物5w的结构。 评价标题化合物,用于抗人免疫缺陷病毒型1(抗HIV-1)和细胞毒性活性。 生物学研究表明,在这些化合物中,5A,B,J,H和I显示了中值的有效浓度(EC50)值小于20μm的活性。 化合物5i表现出最有效的抗HIV-1活性(EC50 =3.2μm),而5h显示抗HIV-1活性(EC50 =3.8μm),主要人淋巴细胞,CEM和VERO细胞中没有毒性。

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