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Enantioselective synthesis of methyl (R)-2-chloromandelate by Saccharomyces cerevisiae

원문정보

Ji-seun KO, Min JEONG, Soon Ho HONG, Ik-keun YOO

피인용수 : 0(자료제공 : 네이버학술정보)

초록

영어

Clopidogrel is a platelet aggregation inhibitor widely administered to atherosclerotic patients with the risk of a heart attack or stroke that are caused by the formation of a clot in the blood. Plavix (clopidogrel bisulfate) is marketed worldwide in nearly 110 countries, with sales of $6.4 billion per year. It had been the second top selling drug in the world for a few years and was still growing by over 20%. Methyl (R)-2-chloromandelate is key intermediate of clopidogrel and should be
enantiopure. Considering the enantioselective nature of enzyme, biological transformation of ketones into optically active alcohols could be an efficient strategy. In the present study, we investigate the factors that influence the reduction of methyl-2-chlorobenzoylformate to find
optimum conditions enabling the efficient production of methyl (R)-2-chloromandelate.[This work was supported by the Small & Medium Business Administration]

키워드

  • Enantioselective synthesis
  • Saccharomyces cerevisiae
  • Methyl (R)-2-chloromandelate
  • clopidogrel bisulfate

저자정보

  • Ji-seun KO School of Chemical Engineering & Bioengineering, University of Ulsan
  • Min JEONG School of Chemical Engineering & Bioengineering, University of Ulsan
  • Soon Ho HONG School of Chemical Engineering & Bioengineering, University of Ulsan
  • Ik-keun YOO School of Chemical Engineering & Bioengineering, University of Ulsan

참고문헌

자료제공 : 네이버학술정보

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