Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Yip, Yvonne"'
Autor:
Gregory P. Donoho, Philip Parker Waid, James A. Cook, Michele C. Smith, David Anthony Barda, Volker Wacheck, Yip Yvonne Yee Mai, Philip W. Iversen, Rose T. Ajamie, Debra A. Young, Mary M. Mader, Douglas J. Zeckner, Manuel Vincente Sanchez-Felix, Everett J. Perkins, Laura J. Bloem
Publikováno v:
Molecular Cancer Therapeutics. 15:2344-2356
The PI3K/AKT/mTOR pathway is among the most frequently altered pathways in cancer cell growth and survival. LY3023414 is a complex fused imidazoquinolinone with high solubility across a wide pH range designed to inhibit class I PI3K isoforms and mTOR
Autor:
John E. Munroe, Q. May Wang, Mark Joseph Tebbe, Frantz Victor, Shu-Hui Chen, Robert B. Johnson, Guo Deqi, Beverly A. Heinz, Jason Eric Lamar, Joseph M. Colacino, John I. Glass, Yip Yvonne Yee Mai
Publikováno v:
Letters in Drug Design & Discovery. 2:118-123
Autor:
Q. May Wang, John I. Glass, Yip Yvonne Yee Mai, Frantz Victor, Shu-Hui Chen, Nathan Yumibe, Robert B. Johnson, Nancy June Snyder, Guo Deqi, Jason Eric Lamar
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:257-261
With the aim of discovering potent and selective HCV protease inhibitors, we synthesized and evaluated a series of 1a based tetrapeptidyl ketoamides with additional modification(s) at P1′, P1, and P3 positions. As a result of this effort, we found
Autor:
Jason Eric Lamar, Ling Jin, Daryl Venable, Lifei Liu, Mark Joseph Tebbe, Frantz Victor, Shu-Hui Chen, Nathan Yumibe, Q. May Wang, Yip Yvonne Yee Mai, Donna Barket, Robert B. Johnson, Joe Colacino, Mark Wakulchik, John E. Munroe, Beverly A. Heinz, John I. Glass, Congping Xie, Elcira C. Villarreal
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:251-256
We describe herein the design, syntheses and evaluation of a number of bicycloproline P2 bearing HCV protease inhibitors endowed with impressive enzyme potency, enzyme selectivity, cellular activity and favorable ADME profiles.
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Autor:
Mark Wakulchik, Q. May Wang, Jason Eric Lamar, Frantz Victor, Shu-Hui Chen, Nathan Yumibe, Robert B. Johnson, John E. Munroe, Yip Yvonne Yee Mai, John I. Glass
Publikováno v:
Bioorganicmedicinal chemistry letters. 14(19)
With the aim of improving HCV protease inhibitors reported in our previous manuscripts, we synthesized and evaluated a series of 1a-based tetrapeptidyl α-ketoamides with additional P4 modification. The promising analog discovered through this SAR, 5
Autor:
Shu-Hui Chen, David X Sun, Beverly A. Heinz, Yip Yvonne Yee Mai, Lifei Liu, Alexander A. Kolykhalov, Jason Eric Lamar, Q. May Wang, Robert B. Johnson
Publikováno v:
Bioorganicmedicinal chemistry letters. 14(16)
We describe herein the design, syntheses, and biological evaluation of new series of P4 tetrazole and adipic acid, ester, amide capped tetrapeptidyl alpha-ketoamide based HCV protease inhibitors.
Autor:
Jason Eric Lamar, Jon A. Erickson, Todd J. Kohn, Mccarthy James R, Hsiu-Chiung Yang, Guo Deqi, Patrick C. May, Shu-Hui Chen, David E. Timm, Yip Yvonne Yee Mai, James McGee
Publikováno v:
Bioorganicmedicinal chemistry letters. 14(1)
With the aim of reducing molecular weight and adjusting log D value of BACE inhibitors to more favorable range for BBB penetration and better bioavailability, we synthesized and evaluated several series of P3 cap modified BACE inhibitors obtained via
Autor:
Chen, Shu-Hui, Lamar, Jason, Guo, Deqi, Kohn, Todd, Yang, Hsiu-Chiung, McGee, James, Timm, David, Erickson, Jon, Yip, Yvonne, May, Patrick, McCarthy, James
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 2004 14(1):245-250
Autor:
Victor, Frantz, Lamar, Jason, Snyder, Nancy, Yip, Yvonne, Guo, Deqi, Yumibe, Nathan, Johnson, Robert B., Wang, Q.May, Glass, John I., Chen, Shu-Hui
Publikováno v:
In Bioorganic & Medicinal Chemistry Letters 2004 14(1):257-261