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微生物的代谢产物。254. 新型多氧霉素假Z和假J的结构

Metabolic products of microorganisms. 254. Structure of the new nikkomycins pseudo-Z and pseudo-J.

作者信息

Heitsch H, König W A, Decker H, Bormann C, Fiedler H P, Zähner H

机构信息

Institute of Organic Chemistry, University of Hamburg, FRG.

出版信息

J Antibiot (Tokyo). 1989 May;42(5):711-7. doi: 10.7164/antibiotics.42.711.

DOI:10.7164/antibiotics.42.711
PMID:2722685
Abstract

Two new nikkomycins were isolated from the fermentation broth of Streptomyces tendae Tü 901/PF 53+-3. These new metabolites, nikkomycins pseudo-Z (psi-Z,1) and pseudo-J (psi-J, 2) differ from the corresponding nikkomycins Z and J by a C-glycosidic bond between C-5 of uracil and C-1' of 5-amino-5-deoxy-D-allo-furanuronic acid instead of an N-glycosidic bond. The structure elucidation was achieved by two-dimensional NMR techniques and mass spectrometry.

摘要

从天蓝色链霉菌Tü 901/PF 53+-3的发酵液中分离出两种新的多氧霉素。这些新的代谢产物,多氧霉素假Z(psi-Z,1)和假J(psi-J,2),与相应的多氧霉素Z和J的区别在于,尿嘧啶的C-5与5-氨基-5-脱氧-D-阿洛呋喃糖醛酸的C-1'之间是C-糖苷键,而不是N-糖苷键。通过二维核磁共振技术和质谱对其结构进行了鉴定。

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