Anthony Paul Ricketts
Pfizer
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Publication
Featured researches published by Anthony Paul Ricketts.
The Journal of Antibiotics | 1990
John P. Dirlam; Annette M. Belton; Jon Bordner; Walter P. Cullen; Liang H. Huang; Yasuhiro Kojima; Hiroshi Maeda; Hiroyuki Nishida; Satoshi Nishiyama; John R. Oscarson; Anthony Paul Ricketts; Tatsuo Sakakibara; Junsuke Tone; Katsuhitsu Tsukuda
A new polyether antibiotic CP-82,009 (C49H84O17) was isolated by solvent extraction from the fermentation broth of Actinomadura sp. (ATCC 53676). Following purification by column chromatography and crystallization, the structure of CP-82,009 was elucidated by spectroscopic (NMR and MS) methods. The absolute stereochemistry was determined by a single crystal X-ray analysis of the corresponding rubidium salt. CP-82,009 is among the most potent anticoccidial agents known, effectively controlling the Eimeria species that are the major causative agents of chicken coccidiosis at doses of 5 mg/kg or less in feed. It is also active in vitro against certain Gram-positive bacteria, as well as the spirochete, Serpulina (Treponema) hyodysenteriae.
Bioorganic & Medicinal Chemistry Letters | 2001
Bruce A. Hay; Bridget Mccarthy Cole; Frank M. DiCapua; Glen W. Kirk; Marianne C. Murray; Rona A. Nardone; Dennis J. Pelletier; Anthony Paul Ricketts; Alan Robertson; Todd W. Siegel
The first potent small molecule sst2 antagonists are reported. Altering known sst2 agonist molecules yielded compounds with high sst2 binding affinity and full antagonist activity. Compound 7a, for example, displaced somatostatin binding to the sst2 receptor with an IC(50)=2.9 nM and antagonized somatostatin action with an IC(50)=29nM.
Journal of Industrial Microbiology & Biotechnology | 1990
John P. Dirlam; Annette M. Belton; Jon Bordner; Walter P. Cullen; Liang H. Huang; Yasuhiro Kojima; Hiroshi Maeda; Satoshi Nishiyama; John R. Oscarson; Anthony Paul Ricketts; Tatsuo Sakakibara; Junsuke Tone; Mamoru Yamada
SummaryA new polyether antibiotic CP-82,996 (C50H86O16) was isolated by solvent extraction from the fermentation broth ofActinomadura sp. (ATCC 63764). Following purification by silica gel column chromatography and crystallization, the structure of CP-82,996 was determined by a single crystal X-ray analysis. The structure is closely related to monensin, but is unique in that it contains two sugar groups, whereas monensin has none. The1H and13C NMR chemical shifts and assignments for CP-82, 996 were elucidated, and they were compared with those determined previously for monensin. CP-82,996 is active against certain Gram-positive bacteria, and is a very potent anticoccidial agent. It effectively controlled chicken coccidiosis caused by severalEimeria species at 5–10 ppm in feed, and is 10–20 times more potent than monensin.
Archive | 2001
Bruce A. Hay; Bridget Mccarthy Cole; Anthony Paul Ricketts
Archive | 2003
Kristin Lundy DeMello; Anthony Paul Ricketts
Archive | 1999
Nigel A. Evans; Carolyn Rose Kilroy; Kristin Marie Lundy; Jean-Pierre St. Lambert Pelletier; Anthony Paul Ricketts
Archive | 2001
Bridget Mccarthy Cole; Anthony Paul Ricketts; Bruce A. Hay
Archive | 2014
James Thomas Anderson; Eugene Lvovich Piatnitski Chekler; Edmund L. Ellsworth; Bruce Kipp Erickson; Adam M. Gilbert; Anthony Paul Ricketts; David P. Thompson; Rayomand Jal Unwalla; Patrick Robert Verhoest
Archive | 1999
Nigel A. Evans; Carolyn Rose Kilroy; Kristin Marie Lundy; Jean-Pierre St. Lambert Pelletier; Anthony Paul Ricketts
Archive | 2007
Leopold Goetze; Anthony Paul Ricketts