J W McFarland, S J Hecker, B H Jaynes, M R Jefson, K M Lundy, C B Vu, E A Glazer, S A Froshauer, S F Hayashi, B J Kamicker, C P Reese, J A Olson
Index: J. Med. Chem. 40(6) , 1041-5, (1997)
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Reductive amination of repromicin with polyfunctional amines has led to new macrolide antibacterial agents, some of which are highly potent against the Gram-negative pathogen Pasteurella multocida both in vitro and in a mouse infection model. A key element in this discovery was the recognition that among certain known macrolides increasing lipophilicity results in diminished in vivo activity. One repromicin derivative, 20-[N-[3-(dimethylamino)-propyl]-N-L-alanylamino]-20-deoxorepro micin (35), was selected for advanced evaluation. At 5 mg/kg, a single subcutaneous dose was found to control induced pasteurellosis in swine and induced respiratory disease in cattle.
Structure | Name/CAS No. | Molecular Formula | Articles |
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rosamicin
CAS:35834-26-5 |
C31H51NO9 |
A new Micromonospora-produced macrolide antibiotic, rosamici...
1972-11-01 [J. Antibiot. 25 , 641, (1972)] |
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2007-04-11 [J. Pharm. Biomed. Anal. 43(5) , 1628-37, (2007)] |
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2003-04-01 [Anal. Bioanal. Chem 375(8) , 1031-7, (2003)] |
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