Literature DB >> 7048060

Structure-activity relationships in the ansamycins. Molecular structure and activity of 3-carbomethoxy rifamycin S.

M Brufani, L Cellai, S Cerrini, W Fedeli, A Segre, A Vaciago.   

Abstract

The X-ray and NMR structural study of 3-carbomethoxy rifamycin S5 was undertaken in order to determine whether its low antimicrobial activity was related to a conformation of the molecule which was unfavorable for interaction with bacterial DNA-dependent RNA polymerase. However, the molecule assumes a conformation similar to that of the active rifamycins. Indeed the compound was found to be active on the isolated enzyme, so that its low activity on whole bacteria has to be attributed to factors affecting its penetration through the bacterial cell wall.

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Year:  1982        PMID: 7048060

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  1 in total

1.  Conformational variety for the ansa chain of rifamycins: comparison of observed crystal structures and molecular dynamics simulations.

Authors:  A Bacchi; G Pelizzi
Journal:  J Comput Aided Mol Des       Date:  1999-07       Impact factor: 3.686

  1 in total

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