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- W4230637863 abstract "The chapter discusses the mode of action of β-lactam antibiotics. Most widely used at present is the “structural analogue” hypothesis based on the structural similarity between penicillins and a possible conformation of the acyl-Dalanyl-D-alanine end of the N-acetylmurarnyl-pentapeptide strand of the bacterial cell wall. A number of experimental data support this hypothesis and the model attractively explains the mechanism of action of β-lactam antibiotics, especially penicillins. The naturally-occurring penicillins and cephalosporins, and thousands of their semisynthetic derivatives, are based on two fundamental structural units, the penam and cepham systems. The numbering of these bicyclic systems is different from that usual for heterocycles. The numbering system for penicillin is also used in the case of cephalosporins and other derivatives, including new members of the group of β-lactam antibiotics." @default.
- W4230637863 created "2022-05-11" @default.
- W4230637863 creator A5004192608 @default.
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- W4230637863 date "1975-01-01" @default.
- W4230637863 modified "2023-09-26" @default.
- W4230637863 title "8 Functional Modifications and Nuclear Analogues of β-Lactam Antibiotics-Part I" @default.
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