Literature DB >> 12323024

Stereostructure of a novel cytotoxic 18-membered macrolactone antibiotic FD-891.

Tadashi Eguchi1, Kayako Kobayashi, Hidehiro Uekusa, Yuji Ohashi, Kazutoshi Mizoue, Yoshitaka Matsushima, Katsumi Kakinuma.   

Abstract

The absolute stereochemistry of FD-891, a novel cytotoxic 18-membered macrolactone antibiotic, was determined by a synthetic approach as well as X-ray diffraction of degradative derivatives. The absolute configuration of FD-891 turned out to be as shown above. The stable conformer of FD-891 was also discussed with respect to biological activity by comparison with the structurally related concanamycin A on the bases of molecular mechanics calculations. [structure: see text]

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Year:  2002        PMID: 12323024     DOI: 10.1021/ol026518k

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Enantioselective total synthesis of FD-891.

Authors:  Michael T Crimmins; Franck Caussanel
Journal:  J Am Chem Soc       Date:  2006-03-15       Impact factor: 15.419

2.  Synthesis by ring-closing metathesis and cytotoxic evaluation of novel thienylmacrolactones.

Authors:  Jürgen Krauss; Daniela Köbler; Verena Miller; Franz Bracher
Journal:  Sci Pharm       Date:  2011-11-01
  2 in total

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