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首页> 外文期刊>Molecules >Substituted Benzamides Containing Azaspiro Rings as Upregulators of Apolipoprotein A-I Transcription
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Substituted Benzamides Containing Azaspiro Rings as Upregulators of Apolipoprotein A-I Transcription

机译:含氮杂螺环的取代苯甲酰胺作为载脂蛋白A-I转录的上调剂。

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摘要

Apolipoprotein A-I (Apo A-I) is the principal protein component of high density lipoprotein (HDL), which is generally considered as a potential therapeutic target against atherosclerosis. The understanding of the Apo A-I regulation mechanism has fuelled the development of novel HDL targeted therapeutic approaches. To identify novel agents that can upregulate Apo A-I expression, we performed a cell-based reporter assay to screen 25,600 small molecules. Based on the dataset obtained from screening, a series of novel analogs of substituted benzamides containing azaspiro rings were assessed for their ability to induce the transcription of the Apo A-I gene, and the structure-activity relationship (SAR) around these analogs was also proposed. The results indicated that the trifluoromethyl substituted benzamide containing an azaspiro ring is a promising backbone for designing Apo A-I transcriptional upregulator and could be viable leads for development of new drugs to prevent and treat atherosclerosis in the future.
机译:载脂蛋白A-I(Apo A-I)是高密度脂蛋白(HDL)的主要蛋白成分,通常被认为是抗动脉粥样硬化的潜在治疗靶标。对Apo A-I调节机制的了解推动了新型HDL靶向治疗方法的发展。为了鉴定可以上调Apo A-I表达的新型药物,我们进行了基于细胞的报告基因检测,筛选出25,600个小分子。基于筛选获得的数据集,评估了一系列含有氮杂螺环的取代苯甲酰胺的新型类似物诱导Apo A-I基因转录的能力,并提出了围绕这些类似物的构效关系(SAR)。结果表明,含有氮杂螺环的三氟甲基取代的苯甲酰胺是设计Apo A-I转录上调剂的有前途的骨架,并且可能是将来开发预防和治疗动脉粥样硬化的新药的可行线索。

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