W
Wanda Cromlish
Researcher at Merck & Co.
Publications - 49
Citations - 5766
Wanda Cromlish is an academic researcher from Merck & Co.. The author has contributed to research in topics: Protein tyrosine phosphatase & Sf9. The author has an hindex of 29, co-authored 49 publications receiving 5558 citations.
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Journal ArticleDOI
Increased insulin sensitivity and obesity resistance in mice lacking the protein tyrosine phosphatase-1B gene.
Mounib Elchebly,Paul Payette,Eva Michaliszyn,Wanda Cromlish,Susan Collins,Ailsa Lee Loy,Denis Normandin,Alan Cheng,Jean Himms-Hagen,Chi-Chung Chan,Chidambaram Ramachandran,Michael J. Gresser,Michel L. Tremblay,Brian P. Kennedy +13 more
TL;DR: In this article, the mouse homolog of the gene encoding PTP-1B yielded healthy mice that, in the fed state, had blood glucose concentrations that were slightly lower and concentrations of circulating insulin that were one-half those of their PTP−1B+/+ littermates.
Journal ArticleDOI
The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K.
Jacques Yves Gauthier,Nathalie Chauret,Wanda Cromlish,Sylvie Desmarais,Le T. Duong,Jean-Pierre Falgueyret,Donald B. Kimmel,Sonia Lamontagne,Serge Leger,Tammy LeRiche,Chun Sing Li,Frédéric Massé,Daniel J. McKay,Deborah A. Nicoll-Griffith,Renata Oballa,James T. Palmer,M. David Percival,Denis Riendeau,Joel Robichaud,Gideon A. Rodan,Sevgi B. Rodan,Carmai Seto,Michel Therien,Vouy-Linh Truong,Michael C. Venuti,Gregg Wesolowski,Robert N. Young,Robert Zamboni,W. Cameron Black +28 more
TL;DR: Odanacatib is a potent, selective, and neutral cathepsin K inhibitor which was developed to address the metabolic liabilities of the Cat K inhibitor L-873724 and was more selective in whole cell assays than the published Cat K inhibitors balicatib and relac atib.
Journal ArticleDOI
The discovery of rofecoxib, [MK 966, VIOXX®, 4-(4′-methylsulfonylphenyl)-3-phenyl-2(5H)-furanone], an orally active cyclooxygenase-2 inhibitor
Petpiboon Prasit,Zhaoyin Wang,Christine Brideau,Chi-Chung Chan,Stella Charleson,Wanda Cromlish,Diane Ethier,Jillian F. Evans,Anthony W. Ford-Hutchinson,Jacques-Yves Gauthier,R. Gordon,Jocelyne Guay,Michael J. Gresser,Stacia Kargman,Brian P. Kennedy,Yves Leblanc,Serge Leger,Joseph A. Mancini,Gary P. O'Neill,Marc Ouellet,M.D. Percival,Helene Perrier,Denis Riendeau,Ian W. Rodger,Philip Tagari,Michael J. Therien,Philip J. Vickers,E. Wong,Lijing Xu,Robert N. Young,Robert Zamboni,Susan Boyce,Nadia M.J. Rupniak,Michael J. Forrest,Denise M. Visco,D Patrick +35 more
TL;DR: The development of a COX-2 inhibitor rofecoxib (MK 966, Vioxx) is described, essentially equipotent to indomethacin both in vitro and in vivo but without the ulcerogenic side effect due toCOX-1 inhibition.
Journal Article
Rofecoxib [Vioxx, MK-0966; 4-(4′-Methylsulfonylphenyl)-3-phenyl-2-(5H)-furanone]: A Potent and Orally Active Cyclooxygenase-2 Inhibitor. Pharmacological and Biochemical Profiles
Chi-Chung Chan,Susan Boyce,Christine Brideau,Stella Charleson,Wanda Cromlish,Diane Ethier,Jillian F. Evans,Anthony W. Ford-Hutchinson,Michael J. Forrest,Jacques-Yves Gauthier,R. Gordon,Michael J. Gresser,Jocelyne Guay,Stacia Kargman,Brian P. Kennedy,Yves Leblanc,Serge Leger,Joseph A. Mancini,Gary P. O'Neill,Marc Ouellet,D Patrick,Percival,Helene Perrier,Petpiboon Prasit,Ian W. Rodger +24 more
TL;DR: Rofecoxib is a novel COX-2 inhibitor with a biochemical and pharmacological profile clearly distinct from that of current nonsteroidal anti-inflammatory drugs and represents a new therapeutic class of anti- inflammatory agents for the treatment of the symptoms of osteoarthritis and rheumatoid arthritis with improved gastrointestinal tolerability.
Journal ArticleDOI
Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX-2 inhibitor.
Denis Riendeau,M.D. Percival,Susan Boyce,Christine Brideau,Stella Charleson,Wanda Cromlish,Diane Ethier,Jillian F. Evans,Jean-Pierre Falgueyret,Anthony W. Ford-Hutchinson,R. Gordon,Gillian Greig,Michael J. Gresser,Jocelyne Guay,Stacia Kargman,Serge Leger,Joseph A. Mancini,Gary P. O'Neill,Marc Ouellet,Ian W. Rodger,Michael J. Therien,Zhaoyin Wang,J.K. Webb,E. Wong,Lijing Xu,Robert N. Young,Robert Zamboni,Petpiboon Prasit,Chi-Chung Chan +28 more
TL;DR: The time‐dependent inhibition by DFU was decreased by co‐incubation with arachidonic acid under non‐turnover conditions, consistent with reversible competitive inhibition at the COX active site.