J. C. Sesnie

In vivo therapeutic efficacies of PD 138312 and PD 140248, two novel fluoronaphthyridines with outstanding gram-positive potency

M. Shapiro, J. Dever, E. Joannides, 1995, Antimicrobial agents and chemotherapy.

New "ofloxacin" type antibacterial agents. Incorporation of the spiro cyclopropyl group at N-1.

M. Schroeder, J. Kiely, J. C. Sesnie, 1988, Journal of medicinal chemistry.

A novel rapid throughput phototolerance screen in mice.

M. Shapiro, C. L. Heifetz, J. Dever, 1996, Journal of pharmacological and toxicological methods.

5″-Amino-5″-Deoxybutirosin, a Semisynthetic Analogue of Butirosin A: Antibacterial Activity In Vitro and in Mice

C. L. Heifetz, I. A. Pearson, J. C. Sesnie, 1976, Antimicrobial Agents and Chemotherapy.

Comparison of microdilution and agar dilution procedures for testing antibiotic susceptibility of Neisseria gonorrhoeae

M. Shapiro, C. L. Heifetz, J. C. Sesnie, 1984, Journal of clinical microbiology.

New 8-(trifluoromethyl)-substituted quinolones. The benefits of the 8-fluoro group with reduced phototoxic risk.

S. Hagen, J. Domagala, M. Shapiro, 1992, Journal of medicinal chemistry.

In vitro evaluation of cefdinir (FK482), a new oral cephalosporin with enhanced antistaphylococcal activity and beta-lactamase stability.

M. Cohen, M. Huband, M. Shapiro, 1994, Diagnostic microbiology and infectious disease.

Quinolone antibacterials: preparation and activity of bridged bicyclic analogues of the C7-piperazine.

J. Kiely, R. Gogliotti, M. P. Hutt, 1991, Journal of Medicinal Chemistry.

Quinolone Antibacterials: Preparation and Activity of Bridged Bicyclic Analogues of the C7‐Piperazine.

J. Kiely, R. Gogliotti, M. P. Hutt, 1991 .