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The chemical structures of streptovirudins.

作者信息

Eckardt K, Ihn W, Tresselt D, Krebs D

出版信息

J Antibiot (Tokyo). 1981 Dec;34(12):1631-2. doi: 10.7164/antibiotics.34.1631.

DOI:10.7164/antibiotics.34.1631
PMID:7333979
Abstract
摘要

相似文献

1
The chemical structures of streptovirudins.链病毒菌素的化学结构。
J Antibiot (Tokyo). 1981 Dec;34(12):1631-2. doi: 10.7164/antibiotics.34.1631.
2
Streptovirudins of series I and II: chemical and biological properties.
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Tunicamycins, streptovirudins, and corynetoxins, a special subclass of nucleoside antibiotics.
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The carbon-13 NMR spectrum of gougerotin.谷氏菌素的碳-13核磁共振谱。
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Carbon-13 nuclear magnetic resonance investigations into the interactions of bisulfite with pyrimidine nucleosides and nucleotides.用碳-13核磁共振研究亚硫酸氢盐与嘧啶核苷及核苷酸的相互作用。
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Alkyl addition reaction of pyrimidine 2'-ketonucleosides: synthesis of 2'-branched-chain sugar pyrimidine nucleosides (nucleosides and nucleotides. LXXXI.
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Fluoro carbocyclic nucleosides: synthesis and antiviral activity of 2'- and 6'-fluoro carbocyclic pyrimidine nucleosides including carbocyclic 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-methyluracil and carbocyclic 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodouracil.氟代碳环核苷:2'-和6'-氟代碳环嘧啶核苷的合成及抗病毒活性,包括碳环1-(2-脱氧-2-氟-β-D-阿拉伯呋喃糖基)-5-甲基尿嘧啶和碳环1-(2-脱氧-2-氟-β-D-阿拉伯呋喃糖基)-5-碘尿嘧啶。
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Bagougeramines A and B, new nucleoside antibiotics produced by a strain of Bacillus circulans. II. Physico-chemical properties and structure determination.巴古胺A和B,由环状芽孢杆菌菌株产生的新型核苷类抗生素。II. 物理化学性质及结构测定
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Pyrimidine nucleosides. V. Reactions of 3-(beta-D-ribofuranosyl)-uracils and related compounds.嘧啶核苷。V. 3-(β-D-呋喃核糖基)-尿嘧啶及相关化合物的反应
J Chem Soc Perkin 1. 1970;13:1869-74. doi: 10.1039/j39700001869.

引用本文的文献

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Selective catalytic hydrogenation of the N-acyl and uridyl double bonds in the tunicamycin family of protein N-glycosylation inhibitors.衣霉素家族蛋白质N-糖基化抑制剂中N-酰基和尿苷基双键的选择性催化氢化反应
J Antibiot (Tokyo). 2017 Dec;70(12):1122-1128. doi: 10.1038/ja.2017.141. Epub 2017 Nov 1.
2
Muraymycin nucleoside-peptide antibiotics: uridine-derived natural products as lead structures for the development of novel antibacterial agents.穆拉霉素核苷肽类抗生素:以尿苷衍生的天然产物作为开发新型抗菌剂的先导结构。
Beilstein J Org Chem. 2016 Apr 22;12:769-795. doi: 10.3762/bjoc.12.77. eCollection 2016.
3
Quinovosamycins: new tunicamycin-type antibiotics in which the α, β-1″,11'-linked N-acetylglucosamine residue is replaced by N-acetylquinovosamine.
奎诺糖霉素:新型衣霉素类抗生素,其中α,β-1″,11'-连接的N-乙酰葡糖胺残基被N-乙酰奎诺糖胺取代。
J Antibiot (Tokyo). 2016 Aug;69(8):637-46. doi: 10.1038/ja.2016.49. Epub 2016 May 18.