Michael J. Castaldi
Pfizer
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Featured researches published by Michael J. Castaldi.
Diagnostic Microbiology and Infectious Disease | 1994
Thomas D. Gootz; Katherine E. Brighty; Marge R. Anderson; Brenda J. Schmieder; Suzanne L. Haskell; Joyce A. Sutcliffe; Michael J. Castaldi; Paul Robert Mcguirk
The in vitro activity of CP-99,219 was compared with that of ciprofloxacin and sparfloxacin against 814 clinical bacterial isolates using a microdilution method with brain-heart infusion broth. CP-99,219 was the most potent agent tested against methicillin-resistant, ciprofloxacin-susceptible staphylocci (minimum inhibitory concentration [MIC]90 < or = 0.25 microgram/ml). CP-99,219 was 32-fold and fourfold more potent than ciprofloxacin and sparfloxacin, respectively, against Streptococcus pneumoniae, including strains resistant to penicillin G and erythromycin (MIC90 < or = 0.25 microgram/ml). CP-99,219 was also the most potent agent tested against S. pyogenes and Enterococcus faecalis (MIC90 < or = 0.5 microgram/ml). The activity of CP-99,219 against Enterobacteriaceae was comparable to that of sparfloxacin, with 90% of Escherichia coli, Enterobacter cloacae, Enterobacter aerogenes, Klebsiella pneumoniae, Citrobacter freundii, C. diversus, Helicobacter pylori, and K. oxytoca being inhibited by < or = 0.5 microgram/ml. Serratia marcescens, Morganella morganii, and Pseudomonas aeruginosa were less susceptible, with MIC90 values to CP-99,219 of 4, 2, and 2 micrograms/ml, respectively. The MIC90 for Bacteroides fragilis was 0.39 microgram/ml for CP-99,219 compared with 12.5 micrograms/ml for ciprofloxacin. CP-99,219 was highly bactericidal at 1 x to 4 x MIC against both Gram-positive and Gram-negative organisms; its activity was similar in nutrient, trypticase soy, and cation-supplemented Mueller-Hinton broths. The spectrum and potency observed with CP-99,219 warrant further testing with this novel quinolone.
Synthetic Communications | 2006
John L. Tucker; Michel Couturier; Michael J. Castaldi; Charles K.-F. Chiu; Detlef Gestmann
Abstract The preparation of the title compound has been revisited and improved. Starting from inexpensive cuminonitrile, 4‐(2‐hydroxy‐2‐methyl)‐ethyl‐benzylamine is obtained in a scalable two‐step process with an overall yield of 55%.
Organic Process Research & Development | 2005
David H. Brown Ripin; Dennis E. Bourassa; Thomas A. Brandt; Michael J. Castaldi; Heather N. Frost; Joel M. Hawkins; Phillip J. Johnson; Stephen S. Massett; Karin Neumann; James Phillips; Jeffery W. Raggon; Peter Robert Rose; Jennifer L. Rutherford; Barbara J. Sitter; A. Morgan Stewart; Michael G. Vetelino; Lulin Wei
Synlett | 2000
Katherine E. Brighty; Michael J. Castaldi
Archive | 2003
Richard A. Buzon; Michael J. Castaldi; Zhengong Bryan Li; David H. Brown Ripin; Yong Tao
Organic Process Research & Development | 2001
John A. Ragan; Jerry Anthony Murry; Michael J. Castaldi; Alyson Kay Conrad; Brian P. Jones; Bryan Li; Teresa W. Makowski; Ruth E. McDermott; Barb J. Sitter; and Timothy D. White; Gregory R. Young
Organic Process Research & Development | 2003
Justin Beaudin; Dennis E. Bourassa; Paul Bowles; Michael J. Castaldi; Ronald J. Clay; Michel Couturier; Gregory L. Karrick; Teresa W. Makowski; Ruth E. McDermott; Clifford N. Meltz; Morgan Meltz; James Phillips; John A. Ragan; David H. Brown Ripin; Robert A. Singer; John L. Tucker; Lulin Wei
Synthesis | 1998
John A. Ragan; Teresa W. Makowski; Michael J. Castaldi; Paul D. Hill
Archive | 2004
Zheng J. Li; Robert J. Rafka; David H. Brown Ripin; Michael J. Castaldi
Archive | 2000
George J. Quallich; Lewin Theophilus Wint; Michael J. Castaldi