It is widely recognized that natural products (NPs) are the most essential source of lead compounds in drug development. Most natural products possess complex structures that can offer a variety of three-dimensional scaffolds, which are useful for scientists to explore a broader chemical space. Biology-oriented synthesis has emerged as an important approach for building natural compound libraries. As an essential biosynthesis approach, diversity-oriented synthesis (DOS) is employed to rapidly and effectively prepare scaffolds and stereochemically diverse molecules.
BOC Sciences has introduced a novel approach: FGPPR technique by using DOS for the simple and rapid construction of natural product libraries containing compounds with diverse and highly complex skeletons.
Figure 1. Classical strategies for the total syntheses of NPs. (Zhang, J.; et al. 2014)
In DOS, the B/F/P (Build/Couple/Pair) strategy is the most widely applied approach which is consist of the following three key steps:
Synthetic blocks are constructed
Then, these building blocks are assembled
Finally, various FGPs reactions are performed to obtain multiple skeletal structures
Figure 2. The process of identification of hidden FGPPs and a optimized B/C/P procedure. (Zhang, J.; et al. 2014)
BOC Sciences has designed novel FGPPR method to synthesize complex molecules with structural diversity using the optimized B/C/P algorithm:
Our scientists perform functional group pairing reactions sequentially to provide NPs and unique natural product-like scaffolds
BOC Sciences provides professional, rapid and high-quality services of Functional Group Pairing Pattern Recognition (FGPPR) at competitive prices for global customers. Personalized and customized services of Functional Group Pairing Pattern Recognition (FGPPR) can satisfy any innovative scientific study demands. Our clients have direct access to our staff and prompt feedback to their inquiries. If you are interested in our services, please contact us immediately!
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BOC Sciences has rich experience in working with global customers in custom library synthesis of compounds and generating small to medium-sized libraries of target compounds. Our knowledge in generating a large number of target molecules in a remarkably shorter time enables quick biological screenings for affinities. With the target properties in mind, we deliver target molecules, by applying our extensive knowledge in drug discovery.