Quantifying biogenic bias in screening libraries.

Quantifying biogenic bias in screening libraries.
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DOI:
10.1038/nchembio.180
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发表时间:
2009-07
影响因子:
14.8
通讯作者:
Shoichet, Brian K.
Shoichet, Brian K.
中科院分区:
生物学1区
文献类型:
--
作者:
Hert, Jerome;Irwin, John J.;Laggner, Christian;Keiser, Michael J.;Shoichet, Brian K.

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在先导发现中,筛选106个分子的文库的生物活性。考虑到超过1060种药物样分子被认为是可能的,这样的筛选可能永远不会成功。即使是偶尔,它们也会这样做,这意味着对文库分子的选择是有偏见的。在这里,开发了一种方法来量化筛选文库对生物源分子的偏倚。通过这种方法,我们考虑筛选文库中缺少什么以及如何优化它们。
In lead discovery, libraries of 106 molecules are screened for biological activity. Given the over 1060 drug-like molecules thought possible, such screens might never succeed. That they do, even occasionally, implies a biased selection of library molecules. Here a method is developed to quantify the bias in screening libraries towards biogenic molecules. With this approach, we consider what is missing from screening libraries and how they can be optimized.
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