Repromicin Derivatives with Potent Antibacterial Activity against <i>Pasteurella multocida</i>

James W. McFarland, Scott J. Hecker, Burton H. Jaynes, Martin R. Jefson, Kristin M. Lundy, Chi B. Vu, Edward A. Glazer, S Froshauer, Shigeru Hayashi, Barbara J. Kamicker,

Journal of Medicinal Chemistry · 1997 · 11 citations · 6 references

Concepts

Abstract

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.

References

6