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Celine M. Bonnefous
Patent Counselor
Patents and Innovations
San Diego
cbonnefous@wsgr.com

D858-350-2213

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Celine Bonnefous is a patent counselor in the San Diego office of Wilson Sonsini Goodrich & Rosati. She assists with the preparation and prosecution of patent applications in the fields of chemistry, pharmaceuticals, and biotechnology.

Prior to joining the firm, Celine was a medicinal chemist at Merck Research Laboratories, Kalypsys, Inc., and Aragon Pharmaceuticals for 14 years. In this role, she performed research in the discovery and development of novel compounds for the treatment of Alzheimer's disease, cancer, pain, anxiety, and metabolic disorders.

Celine received her master's degree in organic chemistry from the University of Houston, where she designed and prepared novel Ru(II) and Cu(I) complexes of 1,10-phenanthroline and di-(2'-pyridyl) ketone based ligands. She is the co-author of more than 20 publications and is listed as a co-inventor on numerous issued and pending U.S. and international patents.

Experience

Celine Bonnefous is a patent counselor in the San Diego office of Wilson Sonsini Goodrich & Rosati. She assists with the preparation and prosecution of patent applications in the fields of chemistry, pharmaceuticals, and biotechnology.

Prior to joining the firm, Celine was a medicinal chemist at Merck Research Laboratories, Kalypsys, Inc., and Aragon Pharmaceuticals for 14 years. In this role, she performed research in the discovery and development of novel compounds for the treatment of Alzheimer's disease, cancer, pain, anxiety, and metabolic disorders.

Celine received her master's degree in organic chemistry from the University of Houston, where she designed and prepared novel Ru(II) and Cu(I) complexes of 1,10-phenanthroline and di-(2'-pyridyl) ketone based ligands. She is the co-author of more than 20 publications and is listed as a co-inventor on numerous issued and pending U.S. and international patents.

Education
  • M.S., Organic Chemistry, University of Houston, 1998
  • B.S., Chemistry, ESCOM (Ecole Supérieure de Chimie Organique et Minérale), 1996
Credentials
Education
  • M.S., Organic Chemistry, University of Houston, 1998
  • B.S., Chemistry, ESCOM (Ecole Supérieure de Chimie Organique et Minérale), 1996

Select Publications

  • Co-author with S. G. Durón, A. Lindstrom, H. Zhang, X. Chen, K. T. Symons, M. Sablad, N. Rozenkrants, Y. Zhang, L. Wang, N. Yazdani, A. K. Shiau, S. A. Noble, P. Rix, T. S. Rao, C. A. Hassig, and N. D. Smith, "Heteroaromatic-aminomethyl Quinolones: Potent and Selective iNOS Inhibitors," 22(2) Bioorganic & Medicinal Chemistry Letters 1237-1241, 2012
  • Co-author with J. E. Payne, J. Roppe, H. Zhuang, X. Chen, K. T. Symons, P. M. Nguyen, M. Sablad, N. Rozenkrants, Y. Zhang, L. Wang, D. Severance, J. P. Walsh, N. Yazdani, A. K. Shiau, S. A. Noble, P. Rix, T. S. Rao, C. A. Hassig, and N. D. Smith, "Discovery of Inducible Nitric Oxide Synthase (iNOS) Inhibitor Development Candidate KD7332, Part 1: Identification of a Novel, Potent, and Selective Series of Quinolinone iNOS Dimerization Inhibitors That are Orally Active in Rodent Pain Models," 52(9) Journal of Medicinal Chemistry 3047-3062, 2009
  • Co-author with J. E. Payne, K. T. Symons, P. M. Nguyen, M. Sablad, N. Rozenkrants, Y. Zhang, L. Wang, N. Yazdani, A. K. Shiau, S. A. Noble, P. Rix, T. S. Rao, C. A. Hassig, and N. D. Smith, "Discovery of Dual Inducible/Neuronal Nitric Oxide Synthase (iNOS/nNOS) Inhibitor Development Candidate 4-((2-Cyclobutyl-1H-imidazo[4,5-b]pyrazin-1-yl)methyl)-7,8-difluoroquinolin-2(1H)-one (KD7332) Part 2: Identification of a Novel, Potent, and Selective Series of Benzimidazole-Quinolinone iNOS/nNOS Dimerization Inhibitors That Are Orally Active in Pain Models," 53(21) Journal of Medicinal Chemistry 7739-7755, 2010
  • Co-author with J. E. Payne, C. A. Hassig, K. T. Symons, X. Guo, P.-M. Nguyen, T. Annable, P. L. Wash, T. Z. Hoffman, T. S. Rao, A. K. Shiau, J. W. Malecha, S. A. Noble, J. H. Hager, and N. D. Smith, "Identification of KD5170: A Novel Mercaptoketone-Based Histone Deacetylase Inhibitor," 18(23) Bioorganic & Medicinal Chemistry Letters 6093-6096, 2008
  • Co-author with J.-M. Vernier, J. H. Hutchinson, M. F. Gardner, M. Cramer, J. K. James, B. A. Rowe, L. P. Daggett, H. Schaffhauser, and T. M. Kamenecka, "Biphenyl-Indanones: Allosteric Potentiators of the Metabotropic Glutamate Subtype 2 Receptor," 15(19) Bioorganic & Medicinal Chemistry Letters 4354-4358, 2005
  • Co-author with J.-M. Vernier, J. H. Hutchinson, J. Chung, G. Reyes-Manalo, and T. M. Kamenecka, "Dipyridyl Amides: Potent Metabotropic Glutamate Subtype 5 (mGlu5) Receptor Antagonists," 15(4) Bioorganic & Medicinal Chemistry Letters 1197-1200, 2005
Insights

Select Publications

  • Co-author with S. G. Durón, A. Lindstrom, H. Zhang, X. Chen, K. T. Symons, M. Sablad, N. Rozenkrants, Y. Zhang, L. Wang, N. Yazdani, A. K. Shiau, S. A. Noble, P. Rix, T. S. Rao, C. A. Hassig, and N. D. Smith, "Heteroaromatic-aminomethyl Quinolones: Potent and Selective iNOS Inhibitors," 22(2) Bioorganic & Medicinal Chemistry Letters 1237-1241, 2012
  • Co-author with J. E. Payne, J. Roppe, H. Zhuang, X. Chen, K. T. Symons, P. M. Nguyen, M. Sablad, N. Rozenkrants, Y. Zhang, L. Wang, D. Severance, J. P. Walsh, N. Yazdani, A. K. Shiau, S. A. Noble, P. Rix, T. S. Rao, C. A. Hassig, and N. D. Smith, "Discovery of Inducible Nitric Oxide Synthase (iNOS) Inhibitor Development Candidate KD7332, Part 1: Identification of a Novel, Potent, and Selective Series of Quinolinone iNOS Dimerization Inhibitors That are Orally Active in Rodent Pain Models," 52(9) Journal of Medicinal Chemistry 3047-3062, 2009
  • Co-author with J. E. Payne, K. T. Symons, P. M. Nguyen, M. Sablad, N. Rozenkrants, Y. Zhang, L. Wang, N. Yazdani, A. K. Shiau, S. A. Noble, P. Rix, T. S. Rao, C. A. Hassig, and N. D. Smith, "Discovery of Dual Inducible/Neuronal Nitric Oxide Synthase (iNOS/nNOS) Inhibitor Development Candidate 4-((2-Cyclobutyl-1H-imidazo[4,5-b]pyrazin-1-yl)methyl)-7,8-difluoroquinolin-2(1H)-one (KD7332) Part 2: Identification of a Novel, Potent, and Selective Series of Benzimidazole-Quinolinone iNOS/nNOS Dimerization Inhibitors That Are Orally Active in Pain Models," 53(21) Journal of Medicinal Chemistry 7739-7755, 2010
  • Co-author with J. E. Payne, C. A. Hassig, K. T. Symons, X. Guo, P.-M. Nguyen, T. Annable, P. L. Wash, T. Z. Hoffman, T. S. Rao, A. K. Shiau, J. W. Malecha, S. A. Noble, J. H. Hager, and N. D. Smith, "Identification of KD5170: A Novel Mercaptoketone-Based Histone Deacetylase Inhibitor," 18(23) Bioorganic & Medicinal Chemistry Letters 6093-6096, 2008
  • Co-author with J.-M. Vernier, J. H. Hutchinson, M. F. Gardner, M. Cramer, J. K. James, B. A. Rowe, L. P. Daggett, H. Schaffhauser, and T. M. Kamenecka, "Biphenyl-Indanones: Allosteric Potentiators of the Metabotropic Glutamate Subtype 2 Receptor," 15(19) Bioorganic & Medicinal Chemistry Letters 4354-4358, 2005
  • Co-author with J.-M. Vernier, J. H. Hutchinson, J. Chung, G. Reyes-Manalo, and T. M. Kamenecka, "Dipyridyl Amides: Potent Metabotropic Glutamate Subtype 5 (mGlu5) Receptor Antagonists," 15(4) Bioorganic & Medicinal Chemistry Letters 1197-1200, 2005

Therapeutics and Drug Discovery

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  • Small molecules

Chemistry and Material Science

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  • Chemistry
  • Organic chemistry
Technical Fluency

Therapeutics and Drug Discovery

  • Pharmacodynamics
  • Pharmacokinetics
  • Small molecule synthesis
  • Small molecules

Chemistry and Material Science

  • Chemical synthesis
  • Chemistry
  • Organic chemistry
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  • Intellectual Property
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