MULTISCAFFOLD · A new strategy for the diversity-oriented synthesis of skeletally diverse alkaloid-like compounds for chemical genetic studies
7РП — „Хора“ (Действия „Мария Кюри“)
- Период
- 2008-11-17 → 2010-11-16
- Финансиране от ЕС
- 169 958 €
- Участници
- 1
- Схема
- MC-IIF
Линиите свързват координатора с партньорите.
Накратко на български
Синтезирани са около 100 нови молекули, подобни на алкалоидите, с различни химични структури. Те служат като инструменти за изследване на биологични механизми в клетки и протеини.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
A new strategy for the diversity-oriented synthesis of skeletally diverse alkaloid-like compounds for chemical genetic studies
Executive summary: The field of chemical genetics – in which small molecules are used as tools to investigate biological mechanisms – requires access to libraries of small molecules that span large tracts of biologically-relevant chemical space. This fellowship resulted in the development of synthetic approaches for preparing skeletally-diverse alkaloid-like small molecules. The fellow exploited the approaches in the synthesis of about 100 alkaloid-like compounds that were based on a wide range of distinct scaffolds. The library of compounds has been offered to a wide range of European cell biologists, funded through EU consortia, for screening in both cell- and protein-based assays.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Chemical Genetics research programmes require libraries of small molecules which span large tracts of biologically-relevant chemical space. Natural products necessarily reside in such chemical space, since they bind both biosynthetic enzymes and target macromolecules. However, natural product partners are not available for most protein targets. Chemical Genetics has spawned diversity-oriented synthesis (DOS), in which libraries of diverse molecules are assembled in up to ca. five steps. The systematic variation of ligand scaffold is particularly challenging, though, despite recent advances in DOS, the diversity of chemical libraries has not yet approached that of natural products because the ligand scaffolds are insufficiently varied. This proposal will focus on the development of new methodology for the synthesis of skeletally diverse alkaloid-like compounds. A multicomponent reaction will be used to define an initial scaffold. A suite of 'scaffold switching' transformations will be developed to allow the initial scaffolds to be transformed into final scaffolds. The methods will be applied to the synthesis of at least 100 alkaloid-like compounds based on at least 10 distinct scaffolds. The library of compounds will be made available, using robotics at Leeds, to European cell biologists for screening in cell- and protein-based assays. The diversity and natural product-like nature means that it is likely to span large tracts of biologically relevant chemical space.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITY OF LEEDS · LeedsКоординаторОбединеното кралство
Връзки
Данни: CORDIS, © Европейски съюз