Literature DB >> 12092820

Short-step syntheses of all stereoisomers of preussin and their bioactivities.

Masayuki Okue1, Hidenori Watanabe, Koji Kasahara, Minoru Yoshida, Sueharu Horinouchi, Takeshi Kitahara.   

Abstract

All the eight stereoisomers of (+)-preussin (1b), an antifungal agent inhibiting the growth of fission yeast and human cancer cells, were synthesized in two steps by non-stereoselective reactions and chromatographic separation, starting from L- and D-N-protected-phenylalaninal (2). Their bioassay revealed all of the stereoisomers to be almost equally bioactive.

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Year:  2002        PMID: 12092820     DOI: 10.1271/bbb.66.1093

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  1 in total

1.  A concise stereoselective synthesis of Preussin, 3-epi-Preussin, and analogues.

Authors:  Myra Beaudoin Bertrand; John P Wolfe
Journal:  Org Lett       Date:  2006-05-25       Impact factor: 6.005

  1 in total

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