Receptor-based design of dihydrofolate reductase inhibitors: comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprim analogues.

By the use of molecular models of Escherichia coli dihydrofolate reductase (DHFR), analogues of trimethoprim (TMP) were designed which incorporated various 3'-carboxyalkoxy moieties in order to acquire ionic interactions with positively charged active-site residues. Certain of these compounds h...

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Bibliografiska uppgifter
Huvudupphovsmän: Kuyper, L, Roth, B, Baccanari, D, Ferone, R, Beddell, C, Champness, J, Stammers, D, Dann, J, Norrington, F, Baker, D
Materialtyp: Journal article
Språk:English
Publicerad: 1985