M
Mark E. Smith
Researcher at University of Missouri–St. Louis
Publications - 5
Citations - 178
Mark E. Smith is an academic researcher from University of Missouri–St. Louis. The author has contributed to research in topics: Cholesterylester transfer protein & Enantiomer. The author has an hindex of 5, co-authored 5 publications receiving 167 citations.
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Journal ArticleDOI
Discovery of Potent, Nonsystemic Apical Sodium-Codependent Bile Acid Transporter Inhibitors (Part 2)
Horng-Chih Huang,Samuel J. Tremont,Len F. Lee,Bradley T. Keller,Carpenter Andrew J,Ching-Cheng Wang,Banerjee Shyamal C,Scott R. Both,Theresa Fletcher,Danny J. Garland,Wei Huang,Claude Jones,Kevin J. Koeller,Kolodziej Steve A,J.-H Li,Robert E. Manning,Matthew W. Mahoney,Miller Raymond E,Deborah A. Mischke,Nigam P. Rath,Emily J. Reinhard,Michael B. Tollefson,William F. Vernier,Grace M. Wagner,Steve R. Rapp,Judy Beaudry,Kevin C. Glenn,Karen Regina,Joe R. Schuh,Mark E. Smith,Jay S. Trivedi,David B. Reitz +31 more
TL;DR: A series of benzothiepines were prepared to refine the structure-activity relationship of the substituted phenyl ring at the 5-position of Benzothiepine ring and to identify potent, crystalline, nonhygroscopic, and efficacious ASBT inhibitors with low systemic exposure.
Journal ArticleDOI
Celecoxib, a selective cyclooxygenase-2 inhibitor, decreases monocyte chemoattractant protein-1 expression and neointimal hyperplasia in the rabbit atherosclerotic balloon injury model.
Kai Wang,Khaldoun G. Tarakji,Zhongmin Zhou,Ming Zhang,Farhad Forudi,Xiaorong Zhou,Alane T. Koki,Mark E. Smith,Bradley T. Keller,Eric J. Topol,A. Michael Lincoff,Marc S. Penn +11 more
TL;DR: It is concluded that celecoxib decreases the inflammatory response and intimal hyperplasia following vascular injury, possibly through inhibition of MCP-1 expression, implying a pivotal role of inflammation in the pathogenesis of restenosis.
Journal ArticleDOI
Discovery of chiral N,N-disubstituted trifluoro-3-amino-2-propanols as potent inhibitors of cholesteryl ester transfer protein.
Richard C. Durley,Margaret L. Grapperhaus,Mark A. Massa,Deborah A. Mischke,Barry L. Parnas,Yvette M. Fobian,Nigam P. Rath,Dorothy D. Honda,Ming Zeng,Daniel T. Connolly,Deborah M. Heuvelman,Bryan J. Witherbee,Kevin C. Glenn,Elaine S. Krul,Mark E. Smith,James A. Sikorski +15 more
Journal ArticleDOI
Chiral N,N-disubstituted trifluoro-3-amino-2-propanols are potent inhibitors of cholesteryl ester transfer protein.
Richard C Durley,Margaret L. Grapperhaus,Brian S Hickory,Mark A. Massa,Jane L Wang,Dale P Spangler,Deborah A. Mischke,Barry L. Parnas,Yvette M. Fobian,Nigam P. Rath,Dorothy D. Honda,Ming Zeng,Daniel T. Connolly,Deborah M. Heuvelman,Bryan J. Witherbee,Michele A Melton,Kevin C. Glenn,Elaine S. Krul,Mark E. Smith,James A. Sikorski +19 more
TL;DR: A novel series of substituted N-benzyl-N-phenyl-trifluoro-3-amino-2-propanols are described that reversibly inhibit cholesteryl ester transfer protein (CETP), and the first reported acyclic CETP inhibitor with submicromolar potency in plasma is reported.
Journal ArticleDOI
Stereospecific inhibition of CETP by chiral N,N-disubstituted trifluoro-3-amino-2-propanols.
Daniel T. Connolly,Bryan J. Witherbee,Michele A. Melton,Richard C. Durley,Margaret L. Grapperhaus,Brad R. McKinnis,William F. Vernier,Maribeth A. Babler,Jeng-Jong Shieh,Mark E. Smith,James A. Sikorski +10 more
TL;DR: These chiral N,N-disubstituted trifluoro-3-amino-2-propanol compounds do not affect lipoprotein structure or CETP-lipoprotein recognition, but inhibit lipid transfer by binding to CETP reversibly and stereospecifically at a site that competes with neutral lipid binding.