
Journal of Antibiotics p. 821 - 832 (1994)
Update date:2022-08-04
Topics: Synthesis Analog Potent activity
Kondo
Ikeda
Ikeda
Takeuchi
Usui
Ishii
Kudo
Gomi
Shibahara
Based on our studies on the enzymatic modifications of arbekacin by methicillin-resistant Staphylococcus aureus (MRSA), replacement of the 2'-hydroxyl group by an amino group in arbekacin was designed to synthesize derivatives that would be active against
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