Jianming BAO - Shanghai, CN Ronald FERGUSON - Rahway NJ, US Xiaolei GAO - Bridgewater NJ, US Scott HARRISON - West Point PA, US Sandra L. KNOWLES - Kenilworth NJ, US Michael Man-chu LO - Kenilworth NJ, US Jeffrey W. SCHUBERT - West Point PA, US - Rahway NJ, US - Shanghai, CN
The present invention is directed to heteroarylpiperidine ether compounds which are allosteric modulators of the M4 muscarinic acetylcholine receptor. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which M4 muscarinic acetylcholine receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which M4 muscarinic acetylcholine receptors are involved.
Preparation And Use Of 7A-Amide Substituted- 6,6-Difluoro Bicyclic Himbacine Derivatives As Par-1 Receptor Antagonists
The present invention relates to bicyclic himbacine derivatives of the formulaand the remaining variables are described herein. The compounds of the invention are effective inhibitors of the PAR-1 receptor. The inventive compounds may be used for the treatment or prophylaxis of disease states such as ASC, secondary prevention of myocardial infarction or stroke, or PAD.
Caltech 2002 - 2007
Doctorates, Doctor of Philosophy, Philosophy, Chemistry
University of California, Berkeley 1996 - 2000
Bachelors, Bachelor of Science, Chemistry
Skills:
Organic Synthesis Medicinal Chemistry Organic Chemistry Drug Discovery Lc Ms Chemistry Drug Design Analytical Chemistry Drug Development Mass Spectrometry Chromatography Synthetic Organic Chemistry Nmr Hplc Purification Nuclear Magnetic Resonance
Boyd Norton, Ronald Rudolph, Marjorie Tootell, Marilyn Leinhos, Joan Harker, Frances Lambert, Bruce Kearsley, Gerald Tierney, Agnes Golden, Philip Lockwood, Walter Martley, Margaret Jenard