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Studies on Novel Bacterial Translocase I Inhibitors, A-500359s. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Structure Elucidation of A-500359 A, C, D and G.
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2003
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In the course of our screening for bacterial phospho-N-acetylmuramyl-pentapeptide-translocase (translocase I: EC 2.7.8.13) inhibitors, we found inhibitory activity in the cultured broth of the strain identified as Streptomyces griseus SANK 60196. The strain produced capuramycin and four novel capuramycin derivatives designated as A-500359 A, C, D and G. Purification and structural analysis were performed, and the structures of A-500359 A, C, D and G were elucidated as 6'''-methylcapuramycin, 3'-demethyl-6'''-methylcapuramycin, 2''-deoxy-6'''-methylcapuramycin and 3'-demethylcapuramycin, respectively.
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1966 | 5.7K | |
1983 | 1.2K | |
1975 | 229 | |
Modes of action of tunicamycin, liposidomycin B, and mureidomycin A: inhibition of phospho-N-acetylmuramyl-pentapeptide translocase from Escherichia coli Philip E. Brandish, Ken‐ichi Kimura, M Inukai, Antimicrobial Agents and Chemotherapy Escherichia ColiAntibacterial Agents TumicamycinAntimicrobial ChemotherapyChemical BiologyDrug Resistance | 1996 | 200 |
1986 | 110 | |
1994 | 89 | |
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1989 | 75 | |
1988 | 40 |
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