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SynthI: A New Open-Source Tool for Synthon-Based Library Design.
Zabolotna, Yuliana; Volochnyuk, Dmitriy M; Ryabukhin, Sergey V; Gavrylenko, Kostiantyn; Horvath, Dragos; Klimchuk, Olga; Oksiuta, Oleksandr; Marcou, Gilles; Varnek, Alexandre.
Afiliação
  • Zabolotna Y; University of Strasbourg, Laboratoire de Chemoinformatique, 4, rue B. Pascal, Strasbourg 67081, France.
  • Volochnyuk DM; Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Murmanska Street 5, Kyiv 02660, Ukraine.
  • Ryabukhin SV; Enamine Ltd.78 Chervonotkatska str., 02660 Kyiv, Ukraine.
  • Gavrylenko K; The Institute of High Technologies, Kyiv National Taras Shevchenko University, 64 Volodymyrska Street, Kyiv 01601, Ukraine.
  • Horvath D; Enamine Ltd.78 Chervonotkatska str., 02660 Kyiv, Ukraine.
  • Klimchuk O; Research-And-Education ChemBioCenter, National Taras Shevchenko University of Kyiv, Chervonotkatska str., 61, 03022 Kyiv, Ukraine.
  • Oksiuta O; Enamine Ltd.78 Chervonotkatska str., 02660 Kyiv, Ukraine.
  • Marcou G; University of Strasbourg, Laboratoire de Chemoinformatique, 4, rue B. Pascal, Strasbourg 67081, France.
  • Varnek A; University of Strasbourg, Laboratoire de Chemoinformatique, 4, rue B. Pascal, Strasbourg 67081, France.
J Chem Inf Model ; 62(9): 2151-2163, 2022 05 09.
Article em En | MEDLINE | ID: mdl-34723532
ABSTRACT
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 (SynthI), 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Indicadores e Reagentes Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Indicadores e Reagentes Idioma: En Ano de publicação: 2022 Tipo de documento: Article