Concepedia

L-155,175: A new antiparasitic macrolide fermentation, isolation and structure.

Michael Goetz, PAMELA A. MCCORMICK, Richard L. Monaghan, D.A. Ostlind, Otto D. Hensens, Jerrold M. Liesch, GEORG ALBERS-SCHÖNBERG

The Journal of Antibiotics · 1985 · 48 citations · 11 references

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Abstract

A new antiparasitic macrolide, L-155,175, produced by a strain of Streptomyces hygroscopicus, has been isolated; its structure was determined by physico-chemical means. It is active against the tapeworm Hymenolepis diminuta in rats.

References

11

Metabolic products of microorganisms. 224. Bafilomycins, a new group of macrolide antibiotics. Production, isolation, chemical structure and biological activity.

Gerhard Werner, Hanspaul Hagenmaier, Hannelore Drautz et al. · The Journal of Antibiotics · 1984 · 330 citations · Full text

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The structure of asukamycin, a possible shunt metabolite from 3-dehydroquinic acid in the shikimate pathway

Nobuo Ikekawa, Akira Nakagawa, Satoshi Ōmura · Journal of the American Chemical Society · 1979 · 75 citations

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<sup>13</sup>C Nuclear Magnetic Resonance Studies. XVI. <sup>13</sup>C Spectra of some Substituted Acrylic Acids and their Methyl Esters. A Correlation of Olefinic Shieldings in α,β-unsaturated Carbonyl Systems

H. Brouwer, J. B. Stothers · Canadian Journal of Chemistry · 1972 · 63 citations

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Structure of the sodium and potassium ion activated adenosine triphosphatase inhibitor L-681,110

Otto D. Hensens, Richard L. Monaghan, Leeyuan Huang et al. · Journal of the American Chemical Society · 1983 · 42 citations

, , +8

The structure of virustomycin A.

Satoshi Ōmura, Nobutaka Imamura, Kiyoizumi Hinotozawa et al. · The Journal of Antibiotics · 1983 · 34 citations · Full text

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