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Cephalosporins, development from natural

It was almost immediately recognised that the deacylated product, 7-aminocephalosporanic add (7-ACA, Figure 6.16), would be of similar importance as was 6-APA in the development of new penidllins. However, 7-ACA, the cephalosporin equivalent of 6-APA, could not be found in fermentations of Cephalosporin acremonium. In Figure 6.15 we have shown that penicillin acylase hydrolyses the acyl residue from natural cephalosporins. Up to a point this is true. These acylases will, however, only work with a limited range of acyl residues. It now seems that nature does not provide for acylases or transacylases that have the capacity to remove or change the D-a-aminoadipyl side chain of cephalosporin C efficiently in a single step. Widespread search for such an enzyme still remains unsuccessful. [Pg.180]

Semi-synthetic penicillins are accessed from 6-aminopenicillanic acid, (6-APA), derived from fermented penicillin G. Starting materials for semi-synthetic cephalosporins are either 7-aminodesacetoxycephalosporanic acid (7-ADCA), which is also derived from penicillin G or 7-aminocephalosporanic acid (7-ACA), derived from fermented cephalosporin C (Scheme 1.10). These three key building blocks are produced in thousands of tonnes annually worldwide. The relatively labile nature of these molecules has encouraged the development of mild biocatalytic methods for selective hydrolysis and attachment of side chains. [Pg.19]

In the period up to 1970 p-lactam research was mainly concerned with the penicillin and cephalosporin groups of compounds (6). Since that time a major extension in the area has taken place with the discovery of several new natural P-lactam structures. In many cases these have features quite different from those present in the penicillins and cephalosporins. This sudden acceleration in discovering new structures has undoubtedly resulted from the design and development of new and sensitive screening procedures. Furthermore new expertise in handling somewhat unstable molecules together with the use of more sophisticated physical, analytical and spectroscopic methods has led to a more rapid determination of structural variations. [Pg.2]


See other pages where Cephalosporins, development from natural is mentioned: [Pg.36]    [Pg.286]    [Pg.303]    [Pg.5]    [Pg.180]    [Pg.7]    [Pg.180]    [Pg.47]    [Pg.288]    [Pg.148]    [Pg.212]    [Pg.288]    [Pg.288]    [Pg.288]    [Pg.407]    [Pg.257]    [Pg.13]    [Pg.223]    [Pg.229]    [Pg.122]    [Pg.1609]    [Pg.220]    [Pg.326]    [Pg.214]    [Pg.125]    [Pg.140]    [Pg.101]   


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Cephalosporins development

Cephalosporins, development from natural products

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