Synthesizing Chiral Drug Intermediates by Biocatalysis
Applied Biochemistry and Biotechnology, ISSN: 1559-0291, Vol: 192, Issue: 1, Page: 146-179
2020
- 51Citations
- 78Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations51
- Citation Indexes51
- 51
- CrossRef41
- Captures78
- Readers78
- 78
Article Description
The chiral feature is a critical factor for the efficacy and safety of many therapeutic agents. At present, about 57% of marketed drugs are chiral drugs and about 99% of purified natural products are chiral compounds. There has been a tremendous potential of functional microorganisms and biocatalysts derived from them for the bioconversion of synthetic chemicals into drugs with high enantio-, chemo-, and regio-selectivities. Biocatalysis is becoming a key subassembly in the medicinal chemist’s toolbox. In fact, the intermediates of many important therapeutic agents such as sitagliptin, pregabalin, ragaglitazar, paclitaxel, epothilone, abacavir, atorvastatin, rosuvastatin, and omapatrilat have been successfully synthesized via biocatalysis. In this review, various biocatalytic systems that enable to synthesize these chiral drug intermediates are updated and discussed regarding their potential application in the pharmaceutical industry. Further development and increased utilization of biocatalysis for production of drugs with emphasis on green chemistry can be expected.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85084073042&origin=inward; http://dx.doi.org/10.1007/s12010-020-03272-3; http://www.ncbi.nlm.nih.gov/pubmed/32323141; https://link.springer.com/10.1007/s12010-020-03272-3; https://dx.doi.org/10.1007/s12010-020-03272-3; https://link.springer.com/article/10.1007/s12010-020-03272-3
Springer Science and Business Media LLC
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