Mutamicins; biosynthetically created new sisomicin analogues.
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Aminoglycosides↗
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Results for “MICROMONOSPORA”
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Incorporation of L-methionine-methyl-14-C into gentamicins. III. Chromatographic separation and degradation of components of methyl-34-C-gentamicin complex.
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Chromatography↗
Letter: Structure of everninomicin C.
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Anti-Bacterial Agents↗
Biosynthesis of rosamicin.
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Aminoglycosides↗
Hybrid biosynthesis and absolute configuration of macrolide antibiotic M-4365 G1.
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Leucomycins↗
A new antibiotic, antlermicin A.
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Aminoglycosides↗
Isolation and identification of N-formylfortimicin A.
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Aminoglycosides↗
Novel antitumor antibiotics, tetrocarcins.
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Aminoglycosides↗
Biosynthetic incorporation of methyl groups into fortimicins.
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Aminoglycosides↗
Dotriacolide, a new beta-lactamase inhibitor.
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Chemical Phenomena↗
The biosynthesis of AR-5 (mycinamicins) antibiotics.
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Anti-Bacterial Agents↗
Biosynthesis of tetrocarcin. Incorporation of 14C- and 13C-labeled compounds into tetrocarcin.
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Aminoglycosides↗
Use of perfluorinated counter ions for the combination of ion pair HPLC and field desorption mass spectrometry. Application to the early characterization of aminoglycoside antibiotics.
The use of perfluorinated carboxylic acids counter ions is described for easy combination of ion pair HPLC and FD-MS. This technique is applied to the analysis of aminoglycoside antibiotics and to the problem of their early characterization from culture broths. Reliable molecular weight informations can be obtained with this method from minute amounts of purified products (10 micrograms) allowing formal identification in most cases.
Aminoglycosides↗
Rustmicin, a new macrolide antibiotic active against wheat stem rust fungus.
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Antifungal Agents↗
Neorustmicin A, a new macrolide antibiotic active against wheat stem rust fungus.
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Antifungal Agents↗
Structures of neorustmicins B, C and D new congeners of rustmicin and neorustmicin A.
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Antifungal Agents↗
Structure of a novel Ca2+ and calmodulin-dependent cyclic nucleotide phosphodiesterase inhibitor K-259-2.
The structure of K-259-2, a potent inhibitor of Ca2+ and calmodulin-dependent cyclic nucleotide phosphodiesterase, was determined to be 3-(2Z-2-ethyl-2-butenyl)-1,6,8-trihydroxy-anthraquinone-2-carboxyl ic acid by chemical conversion and spectral studies.
Magnetic Resonance Spectroscopy↗
Izenamicins: macrolide antibiotics.
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Aminoglycosides↗