Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 6. Structure−Activity Studies of Orally Bioavailable, 2-Pyridone-Containing Peptidomimetics

Author:

Dragovich Peter S.1,Prins Thomas J.1,Zhou Ru1,Brown Edward L.1,Maldonado Fausto C.1,Fuhrman Shella A.1,Zalman Leora S.1,Tuntland Tove1,Lee Caroline A.1,Patick Amy K.1,Matthews David A.1,Hendrickson Thomas F.1,Kosa Maha B.1,Liu Bo1,Batugo Minerva R.1,Gleeson Jean-Paul R.1,Sakata Sylvie K.1,Chen Lijian1,Guzman Mark C.1,Meador James W.1,Ferre Rose Ann1,Worland Stephen T.1

Affiliation:

1. Pfizer Global Research and Development-La Jolla/Agouron Pharmaceuticals, Inc., 10777 Science Center Drive, San Diego, California 92121-1111

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Reference73 articles.

1. (a) Couch, R. B. Rhinoviruses. InFieldsVirology, 3rd ed.; Fields, B. N., Knipe, D. M., Howley, P. M., et al., Eds.; Lippincott-Raven Publishers:  Philadelphia, 1996; Vol. 1, Chapter 23, pp 713−734.

2. TREATMENT OF THE PICORNA VIRUS COMMON COLD BY INHIBITORS OF VIRAL UNCOATING AND ATTACHMENT

3. RHINOVIRUS COLDS

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