University of Strasbourg, Laboratoire de Chemoinformatique, 4, rue B. Pascal, Strasbourg 67081, France.
Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Murmanska Street 5, Kyiv 02660, Ukraine.
J Chem Inf Model. 2022 May 9;62(9):2151-2163. doi: 10.1021/acs.jcim.1c00754. Epub 2021 Nov 1.
Most of the existing computational tools for de novo library design are focused on the generation, rational selection, and combination of promising structural motifs to form members of the new library. However, the absence of a direct link between the chemical space of the retrosynthetically generated fragments and the pool of available reagents makes such approaches appear as rather theoretical and reality-disconnected. In this context, here we present Synthons Interpreter (), a new open-source toolkit for de novo library design that allows merging those two chemical spaces into a single synthons space. Here synthons are defined as actual fragments with valid valences and special labels, specifying the position and the nature of reactive centers. They can be issued from either the "breakup" of reference compounds according to 38 retrosynthetic rules or real reagents, after leaving group withdrawal or transformation. Such an approach not only enables the design of synthetically accessible libraries and analog generation but also facilitates reagents (building blocks) analysis in the medicinal chemistry context. SynthI code is publicly available at https://github.com/Laboratoire-de-Chemoinformatique/SynthI.
大多数从头设计库的现有计算工具都集中在生成、合理选择和组合有前途的结构基序,以形成新库的成员。然而,反合成生成的片段的化学空间与可用试剂库之间没有直接联系,使得这些方法显得相当理论化,与现实脱节。在这种情况下,我们在这里提出了 Synthons Interpreter (),这是一个新的开源从头设计库的工具包,它允许将这两个化学空间合并到一个单个的 synthons 空间中。在这里,synthons 被定义为具有有效价态和特殊标签的实际片段,指定反应中心的位置和性质。它们可以从根据 38 个反合成规则对参考化合物的“断裂”中产生,或者在离去基团消除或转化后从真实试剂中产生。这种方法不仅能够设计可合成的文库和类似物的生成,还能够促进药物化学背景下的试剂(构建块)分析。SynthI 代码可在 https://github.com/Laboratoire-de-Chemoinformatique/SynthI 上公开获得。