Advinus Therapeutics Cempra Taxis
Scientific Advisory Board Member
Bristol-Myers Squibb 1969 - 2006
Senior Vice President, Pharmaceutical Development
Cmc Development 1969 - 2006
Principal
Education:
Columbia University In the City of New York 1968 - 1969
Purdue University 1964 - 1968
Doctorates, Doctor of Philosophy, Organic Chemistry
Skills:
Biotechnology Gmp Pharmaceutical Industry Lifesciences Drug Discovery Project Management R&D Oncology Product Development Hplc Technology Transfer Medicinal Chemistry Competitive Intelligence Drug Design Drug Development Clinical Development Chemistry Analytical Chemistry Cro Regulatory Affairs Organic Chemistry
George Paffendorf - Hackettstown NJ, US Christopher M. Cimarusti - Manalapan NJ, US
International Classification:
A61K 36/37
US Classification:
424759
Abstract:
Products derived from the Hook F (TwHF) plant in the form of extracts are provided that are useful in preventing, treating, or ameliorating a symptom of an inflammatory disorder or an immune disorder, such as an auto-immune disease. Also provided are methods of freeze-drying a TwHF root and/or root portion, methods of debarking a freeze-dried TwHF root and/or root portion, methods of preparing and/or refining extracts in freely flowable solid form from freeze-dried debarked TwHF roots and/or root portions, and methods of using freely flowable solid extracts of TwHF in preventing, treating or ameliorating a symptom of an inflammatory disorder and/or an immune disorder.
Perhydrofluorenetetrol And Perhydrophenanthrenetetrol Derivatives
Frederic Peter Hauck - Somerville NJ Christopher Michael Cimarusti - Somerset NJ
Assignee:
E. R. Squibb & Sons, Inc. - Princeton NJ
International Classification:
C07D29502 C07D29508 C07D29514
US Classification:
544380
Abstract:
Compounds are provided having the structure ##STR1## wherein n is 1 or 2, n. sup. 1 is 0, 1 or 2 and n. sup. 2 is 0, 1, 2 or 3, R. sub. 1, R. sub. 2, R. sub. 3 and R. sub. 4 may be the same or different and can be hydrogen, lower alkyl, halolower alkyl, acyl, lower alkoxy-carbonyl ##STR2## amido ##STR3## or lower alkoxyalkylene, R can be lower alkoxy, lower alkyl or cycloalkyl, R. sub. 8 can be hydrogen, lower alkyl, cycloalkyl, hydroxy, dialkylaminoalkyl or R. sub. 9 O(CH. sub. 2)q-. X is a single bond or a straight or branched bivalent aliphatic radical and Y is ##STR4## These compounds are useful in the treatment of hypertension.
Steroidal[16.Alpha.,17-B]1,4-Dioxanes And Steroidal[16.Alpha.,17-B]1,4-Dioxins
Christopher M. Cimarusti - Hamilton NJ Seymour D. Levine - North Brunswick NJ Frank L. Weisenborn - Titusville NJ
Assignee:
E. R. Squibb & Sons, Inc. - Princeton NJ
International Classification:
C07J 500
US Classification:
26023955R
Abstract:
A series of novel steroidal [[16. alpha. ,17-b]1,4-dioxanes and steroidal [ 16. alpha. ,17-b]1,4-dioxins having useful anti-inflammatory properties is disclosed herein.
Process And Intermediates For Beta-Lactams Having Aminothiazole(Iminooxyacetic Acid)Acetic Acid Sidechains
Theodor Denzel - Regensburg, DE Christopher M. Cimarusti - Millstone NJ Janak Singh - Lawrenceville NJ Richard H. Mueller - Ringoes NJ
Assignee:
E. R. Squibb & Sons, Inc. - Princeton NJ
International Classification:
C07D41714 C07D50138
US Classification:
540222
Abstract:
Disclosed herein are processes for preparing a compound of the formula ##STR1## in which a novel compound of the formula ##STR2## is reacted with a beta lactam of the formula ##STR3## by treatment with a base, wherein the symbols are as defined in the specification.
Christopher M. Cimarusti - Hamilton NJ Paul Wojtkowski - Wilmington DE Joseph E. Dolfini - Cincinnati OH
Assignee:
E. R. Squibb & Sons, Inc. - Princeton NJ
International Classification:
C07D50120
US Classification:
260243C
Abstract:
Thio-. beta. -lactam cephalosporins of the general formula ##STR1## wherein R is hydrogen, lower alkyl, phenyl-lower alkyl, trihaloethyl, alkali metal or alkaline earth metal; R. sub. 1 is hydrogen, lower alkyl, cycloalkyl, phenyl, phenoxy, phenyl-lower alkyl or certain heterocyclic groups; R. sub. 2 is hydrogen, amino, carboxy, hydroxy or ureido; and X is hydrogen, hydroxy, lower alkylthio, lower alkylthiadiazolyl, lower alkyltetrazolyl or lower alkanoyloxy, are useful as antimicrobial agents.
Frederic Peter Hauck - Somerville NJ Joyce Reid - Highland Park NJ Venkatachala L. Narayanan - Hightstown NJ Christopher M. Cimarusti - Hamilton NJ Rudiger D. Haugwitz - Titusville NJ Joseph E. Sundeen - Yardley PA
Assignee:
E. R. Squibb & Sons, Inc. - Princeton NJ
International Classification:
C07D21122
US Classification:
26029356
Abstract:
Compounds are provided having the structure ##STR1## WHEREIN N IS 1, 2 OR 3, M AND M' ARE 0, 1 OR 2, R. sub. 1, R. sub. 2, R. sub. 3 and R. sub. 4 may be the same or different and can be hydrogen, lower alkyl, halolower alkyl, acyl, lower alkoxy-carbonyl ##STR2## or lower alkoxyalkylene, X is a straight or branched bivalent aliphatic radical and Y is ##STR3## These compounds are useful in the treatment of hypertension.
4,7-Dihydroindanyl Alkanols, Analogues Thereof And Their Corresponding Tosylates
Frederic Peter Hauck - Somerville NJ Joyce Reid - Highland Park NJ Venkatachala L. Narayanan - Hightstown NJ Christopher M. Cimarusti - Hamilton NJ Rudiger D. Haugwitz - Titusville NJ Joseph E. Sundeen - Yardley PA
Assignee:
E. R. Squibb & Sons, Inc. - Princeton NJ
International Classification:
C07C14368 C07C 3302 C07C 3532 C07C 3536
US Classification:
260456P
Abstract:
Compounds are provided having the structure ##STR1## WHEREIN N IS 1, 2 OR 3, M AND M' ARE 0, 1, OR 2, R. sub. 1, R. sub. 2, R. sub. 3 and R. sub. 4 may be the same or different and can be hydrogen, lower alkyl, halolower alkyl, acyl, lower alkoxy-carbonyl ##STR2## or lower alkoxyalkylene, X is a straight or branched bivalent aliphatic radical and Y is ##STR3## These compounds are useful in the treatment of hypertension.
William A. Slusarchyk - Belle Mead NJ Christopher M. Cimarusti - Hamilton NJ
Assignee:
E. R. Squibb & Sons, Inc. - Princeton NJ
International Classification:
C07D50120
US Classification:
544 30
Abstract:
Cephalosporin intermediates of the formulas ##STR1## wherein R is lower alkyl, 2,2,2-trichloroethyl, diphenylmethyl, p-methoxybenzyl, or p-nitrobenzyl; R. sub. 1 is lower alkyl or phenyl; R. sub. 2 is hydrogen or acetoxy; R. sub. 4 is methyl or ethyl; and R. sub. 5 is hydrogen, methyl, or methoxy; are disclosed. Methods of reacting these intermediates to prepare antibacterially active cephalosporins are disclosed.
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