Abstract
Many tetracyclines with a similar chemical structure and virtually the same spectrum of antimicrobial activity have become available since their introduction in 1948. A vast literature on them has sprung up and a number of detailed accounts of the tetracyclines and their development have been published (Kucers, 1972; Garrod et al., 1973; Murdoch, 1974). The most commonly used members of the tetracycline group are: tetracycline itself (the parent compound), Oxytetracycline, Chlortetracycline, demeclocycline (demethylchlortetracycline), and in more recent years, lymecycline, rolitetracycline, methacycline, clomocycline (chlormethylencycline), doxycycline and minocycline. While there are some individual differences between the various agents, they can be considered as a group.
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References
Finland, M.: Twenty-fifth anniversary of the discovery of Aureomycin: The place of the tetracyclines in antimicrobial therapy. Clinical Pharmacology and Therapeutics 15: 3–8 (1974).
Garrod, L.P.; Lambert, H.P. and O’Grady, R.: Tetracyclines; in Antibiotic and Chemotherapy, 4th ed, p. 149–166 (Churchill Livingstone, Edinburgh and London 1973).
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© 1978 ADIS Press
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Ball, A.P., Gray, J.A., Murdoch, J.M. (1978). The Tetracyclines. In: Antibacterial Drugs Today. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-8004-7_8
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DOI: https://doi.org/10.1007/978-94-011-8004-7_8
Publisher Name: Springer, Dordrecht
Print ISBN: 978-0-85200-505-7
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