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Polyene macrolide antibiotic amphotericin B. Crystal structure of the N-iodoacetyl derivative

✍ Scribed by Ganis, Paolo; Avitabile, Gustavo; Mechlinski, Witold; Schaffner, Carl P.


Book ID
118200494
Publisher
American Chemical Society
Year
1971
Tongue
English
Weight
587 KB
Volume
93
Category
Article
ISSN
0002-7863

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Structure and absolute configuration of
✍ W. Mechlinski; C.P. Schaffner; P. Ganis; G. Avitabile πŸ“‚ Article πŸ“… 1970 πŸ› Elsevier Science 🌐 French βš– 197 KB

As a result of the x-ray single crystal analysis of N-iodoacetylamphotericin B the chemical and stereochemical absolute structure ia presented (I). A similar etructure and stereochemistry wae extended to the parent compound itself, amphotericin B, a heptaene macrolide antifungal antibiotic possessin

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Tetrahedron Letters No. 41. pp. 3601-3604 (1970) p. 3529 W. Sprenger was omitted from the "Contributors to this issue" W. MECHLINSKI, C. P. SCHAFFNER, P. GANIS and G. AVITABILE: Structure and absolute configuration of the polyene macrolide antibiotic amphotericin B.

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Complete mass spectra of the pertrimethylsilylated derivatives of three high molecular weight polyene macrolide antibiotics are reported for the first time. The fragmentation pathways which are proposed have been corroborated by the stable isotope derivatives d,-TMS and d,-acetyl. Accurate mass meas

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Amphotericin B (AmB) exhibits immunomodulating properties in mice. In vitro studies on lymphocytes, in relation with these properties, are reported here with AmB and two of its derivatives: the N-Fructosyl (N-Fru AmB) and the N-thiopropionyl (AmBSH) derivatives. Interactions of these molecules with