Literature DB >> 885805

Macrolide antibiotics M-4365 produced by Micromonospora. II. Chemical structures.

A Kinumaki, K I Harada, T Suzuki, M Suzuki, T Okuda.   

Abstract

By physiochemical analyses and chemical procedures, the structures of a series of basic 16-membered macrolide antibiotics, M-4365, A1, A2, A3, G1, G2 and G3 were elucidated, and it was found that M-4365 A1, G1 and G2 were novel, while M-4365 A2, A3 and G3 were identical with rosamicin, juvenimicins A4 and B1, respectively.

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Year:  1977        PMID： 885805     DOI： 10.7164/antibiotics.30.450

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


  3 in total

Review 1.  Astonishing diversity of natural surfactants: 2. Polyether glycosidic ionophores and macrocyclic glycosides.

Authors:  Valery M Dembitsky
Journal:  Lipids       Date:  2005-03       Impact factor: 1.880

2.  Function of cytochrome P450 enzymes RosC and RosD in the biosynthesis of rosamicin macrolide antibiotic produced by Micromonospora rosaria.

Authors:  Yohei Iizaka; Noriko Higashi; Masanari Ishida; Reina Oiwa; Yumi Ichikawa; Moeka Takeda; Yojiro Anzai; Fumio Kato
Journal:  Antimicrob Agents Chemother       Date:  2012-12-28       Impact factor: 5.191

3.  Chemoenzymatic Total Synthesis and Structural Diversification of Tylactone-Based Macrolide Antibiotics through Late-Stage Polyketide Assembly, Tailoring, and C-H Functionalization.

Authors:  Andrew N Lowell; Matthew D DeMars; Samuel T Slocum; Fengan Yu; Krithika Anand; Joseph A Chemler; Nisha Korakavi; Jennifer K Priessnitz; Sung Ryeol Park; Aaron A Koch; Pamela J Schultz; David H Sherman
Journal:  J Am Chem Soc       Date:  2017-06-05       Impact factor: 15.419
  3 in total

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