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Selective inhibition of the bacterial translocase reaction in peptidoglycan synthesis by mureidomycins.

Mureidomycins (MRDs) A and C inhibited strongly the formation of undecaprenyl pyrophosphoryl N-acetylmuramyl-pentapeptide (lipid intermediate I), which is an intermediate in bacterial peptidoglycan synthesis (50% inhibitory concentration [IC50] of MRD A, 0.05 microgram/ml). However, they did not inh...

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Hlavní autoři: Inukai, M, Isono, F, Takatsuki, A
Médium: Artigo
Jazyk:Inglês
Vydáno: 1993
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC187869/
https://ncbi.nlm.nih.gov/pubmed/8517724
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