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Identification of Orthologous Target Pairs with Shared Active Compounds and Comparison of Organism-specific Activity Patterns

机译:具有共享活性化合物的直系同源靶标的鉴定和生物特异性活性模式的比较

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摘要

A systematic search for active small molecules shared by orthologous targets was carried out, leading to the identification of 803 compound-based orthologous target pairs covering a total of 938 orthologues, 358 unique targets and 98 organisms. Many orthologous target pairs were found to have substantial compound coverage, enabling the introduction of an orthologous target pairs classification including 'organism cliffs' and 'potency-retaining' pairs. A total of 158 orthologous target pairs involving human orthologues were identified, which were typically associated with drug discovery-relevant targets, organism combinations and compound data. Orthologous target pairs with human orthologues included 83 potency-retaining orthologous target pairs covering a variety of targets and organisms. On the basis of these orthologous target pairs, the compound search was further extended and 1149 potent compounds were identified that only had reported activities for non-human orthologues of 48 therapeutic targets, but not their human counterparts, hence providing a large pool of candidate compounds for further evaluation. The complete set of orthologous target pairs identified in our analysis, the orthologous target pairs classification including associated data and all candidate compounds are made freely available.
机译:系统地搜索了直系同源靶标共有的活性小分子,从而鉴定了803个基于化合物的直系同源靶标对,涵盖了总共938个直系同源物,358个独特靶标和98个生物。发现许多直系同源靶对具有相当大的化合物覆盖范围,从而可以引入直系同源靶对分类,包括“生物悬崖”和“保持力”对。总共确定了158个涉及人类直系同源物的直系同源靶标对,这些对通常与药物发现相关的靶标,生物组合和化合物数据相关。与人类直系同源物的直系同源靶对包括涵盖各种靶标和生物的83种保持力的直系同源靶标对。在这些直系同源靶标的基础上,进一步扩展了化合物的搜索范围,并鉴定出1149种有效化合物,这些化合物仅报告了48种治疗靶标的非人类直系同源物的活性,但未报告其人类对应物的活性,因此提供了大量候选化合物进行进一步评估。我们的分析中确定了完整的直系同源靶对,包括相关数据和所有候选化合物的直系同源靶对分类可免费获得。

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