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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)亚乙基)-2-(5,5-二氧化物-3-苯基苯并[e]吡唑并[4,3-c] [1,2]的合成及抗HIV-1筛选噻嗪-4(1H)-基)乙酰肼。

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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)亚乙基)-2-(5,5-二氧-3-苯基苯并[e]吡唑并[4,3-c] [1,2]噻嗪-4(1H)合成了β-基)乙酰肼。通过热方法以及超声浴进行合成以减少反应时间并提高产物产率。通过诸如NMR,红外和EIMS的光谱技术来表征合成的化合物。通过X射线晶体学阐明了化合物5w的结构。评价标题化合物的抗人免疫缺陷病毒1型(抗HIV-1)和细胞毒活性。生物学研究表明,在这些化合物中,5a,b,j,h和i显示的活性为中值有效浓度(EC50)值小于20μM。化合物5i表现出最有效的抗HIV-1活性(EC50 = 3.2μM),而化合物5i显示出抗HIV-1活性(EC50 = 3.8μM),在原代人淋巴细胞,CEM和VERO细胞中完全没有毒性。

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