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G. Hartmann, K. Honikel, F. Knüsel, J. Nüesch (1967)
The specific inhibition of the DNA-directed RNA synthesis by rifamycin.Biochimica et biophysica acta, 145 3
W. Wehrli, F. Knüsel, K. Schmid, M. Staehelin (1968)
Interaction of rifamycin with bacterial RNA polymerase.Proceedings of the National Academy of Sciences of the United States of America, 61 2
S. Boyden (1951)
THE ADSORPTION OF PROTEINS ON ERYTHROCYTES TREATED WITH TANNIC ACID AND SUBSEQUENT HEMAGGLUTINATION BY ANTIPROTEIN SERAThe Journal of Experimental Medicine, 93
N. Maggi, C. Pasqualucci, R. Ballotta, P. Sensi (1966)
Rifampicin: a new orally active rifamycin.Chemotherapy, 11 5
J. Subak-Sharpe, M. Timbury, J. Williams (1969)
Rifampicin inhibits the Growth of Some Mammalian VirusesNature, 222
W. Wehrli, J. Nüesch, F. Knüsel, M. Staehelin (1968)
Action of rifamycins on RNA polymerase.Biochimica et biophysica acta, 157 1
RIFAMPICIN—3 - (4 - methyl - l -piperazyl - iminomethyl) -rifamycin SV—a semi-synthetic derivative of rifamycin which was isolated from Streptomyces mediterraneus 1, is a clinically useful, orally active antibiotic. Even at low concentrations (0.5–5 µg/ml.), it is known to inhibit microbial growth by blocking cellular DNA-directed RNA polymerase (EC 2.7.7.6)2,3. Although similar inhibition of RNA synthesis does not occur in mammalian cell-free systems unless large amounts of rifampicin (200 µg/ml.) are used4, concentrations exceeding 10 µg of rifampicin/ml. medium cause detectable damage in the case of monolayer cultures of BHK21 C 13 cells5.
Nature – Springer Journals
Published: Dec 19, 1970
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