Literature DB >> 10395273

Feglymycin, a novel inhibitor of the replication of the human immunodeficiency virus. Fermentation, isolation and structure elucidation.

L Vértesy1, W Aretz, M Knauf, A Markus, M Vogel, J Wink.   

Abstract

The novel peptide feglymycin has been isolated from cultures of Streptomyces sp. DSM 11171 by solid phase extraction, size exclusion chromatography and repeated reversed-phase chromatography. The molecular weight was found to be 1900.90 g/mol and the molecular formula is C95H97Nl3O30. Feglymycin contains 13 amino acids of which four are 3-hydroxyphenylglycine and five are 3,5-dihydroxyphenylglycine residues. The structure of the linear peptide has been determined by 1H and 13C NMR spectroscopy. The sequence was confirmed by the observed mass spectroscopic fragmentation pattern. As well as having weak antibacterial activity, feglymycin inhibits the replication of the human immunodeficiency virus (HIV) in vitro.

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Year:  1999        PMID: 10395273     DOI: 10.7164/antibiotics.52.374

Source DB:  PubMed          Journal:  J Antibiot (Tokyo)        ISSN: 0021-8820            Impact factor:   2.649


  8 in total

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Authors:  Victoria T Lim; Sergey V Tsukanov; Amanda B Stephens; Jeffrey N Johnston
Journal:  Organic Synth       Date:  2016

4.  Total synthesis of feglymycin based on a linear/convergent hybrid approach using micro-flow amide bond formation.

Authors:  Shinichiro Fuse; Yuto Mifune; Hiroyuki Nakamura; Hiroshi Tanaka
Journal:  Nat Commun       Date:  2016-11-28       Impact factor: 14.919

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7.  A New Micromonospora Strain with Antibiotic Activity Isolated from the Microbiome of a Mid-Atlantic Deep-Sea Sponge.

Authors:  Catherine R Back; Henry L Stennett; Sam E Williams; Luoyi Wang; Jorge Ojeda Gomez; Omar M Abdulle; Thomas Duffy; Christopher Neal; Judith Mantell; Mark A Jepson; Katharine R Hendry; David Powell; James E M Stach; Angela E Essex-Lopresti; Christine L Willis; Paul Curnow; Paul R Race
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8.  Silyl imine electrophiles in enantioselective catalysis: a Rosetta Stone for peptide homologation, enabling diverse N-protected aryl glycines from aldehydes in three steps.

Authors:  Dawn M Makley; Jeffrey N Johnston
Journal:  Org Lett       Date:  2014-05-14       Impact factor: 6.005

  8 in total

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