Abstract: The present application provides for a compound of Formula I, or a pharmaceutically acceptable salt, solvate, and/or ester thereof, compositions containing such compounds, therapeutic methods that include the administration of such compounds, and therapeutic methods and include the administration of such compounds with at least one additional therapeutic agent.
Type:
Grant
Filed:
July 6, 2007
Date of Patent:
November 29, 2011
Assignee:
Gilead Sciences, Inc.
Inventors:
Manoj C. Desai, Allen Y. Hong, Hongtao Liu, Randall W. Vivian, Lianhong Xu
Abstract: The present application provides for a compound of Formula I, or a pharmaceutically acceptable salt, solvate, and/or ester thereof, compositions containing such compounds, therapeutic methods that include the administration of such compounds, and therapeutic methods and include the administration of such compounds with at least one additional therapeutic agent.
Type:
Grant
Filed:
July 6, 2007
Date of Patent:
May 10, 2011
Assignee:
Gilead Sciences, Inc.
Inventors:
Manoj C. Desai, Allen Yu Hong, Hongtao Liu, Randall W. Vivian, Lianhong Xu
Abstract: A novel method has led to the identification of novel mixed ester-amidates of PMPA for retroviral or hepadnaviral therapy, including compounds of structure (5a) having substituent groups as defined herein. Compositions of these novel compounds in pharmaceutically acceptable excipients and their use in therapy and prophylaxis are provided.
Type:
Grant
Filed:
April 28, 2008
Date of Patent:
September 28, 2010
Assignee:
Gilead Sciences, Inc.
Inventors:
Mark W. Becker, Harlan H. Chapman, Tomas Cihlar, Eugene J. Eisenberg, Gong-Xin He, Michael R. Kernan, William A. Lee, Ernest J. Prisbe, John C. Rohloff, Mark L. Sparacino
Abstract: Prochiral ketones are enantioselectively reduced to chiral secondary alcohols with a compound having the formula I:
where, the two R2 groups are identical and are each a substituted or unsubstituted, aryl, alkyl, cycloalkyl or aralkyl group; and R3 is a hydrogen atom or a substituted or unsubstituted, alkyl, aryl, aralkyl or alkoxy group; wherein the substituents on the R2 and R3 groups are substantially non-reactive.
Abstract: Methods are provided for treating proliferative diseases, especially cancers, comprising administering (1) a farnesyl protein transferase inhibitor in conjunction with (2) an antineoplastic agent and/or radiation therapy.
Type:
Grant
Filed:
February 14, 2000
Date of Patent:
December 25, 2001
Assignee:
Schering Corporation
Inventors:
Walter R. Bishop, Joseph J. Catino, Ronald J. Doll, Ashit Ganguly, Viyyoor M. Girijavallabhan, Paul Kirschimeier, Ming Liu, Loretta L. Nielsen, David L. Cutler
Abstract: Methods are provided for treating cancer, comprising administering (1) a farnesyl protein transferase inhibitor in conjunction with (2) an additional Ras signaling pathway inhibitor to induce cancer cell death and tumor regression.
Type:
Grant
Filed:
April 9, 1999
Date of Patent:
November 13, 2001
Assignee:
Schering Corporation
Inventors:
Walter R. Bishop, Diana L. Brassard, Tattanahalli L. Nagabhushan
Abstract: Methods are disclosed for treating cancer in a patient in need of such treating comprising administering temozolomide in an amount effective to achieve a clinical response wherein the temozolomide is administered in a microcrystalline suspension.
Abstract: Novel compounds of formula
are disclosed. Also disclosed is a method of inhibiting farnesyl protein transferase function and therefore inhibiting the abnormal growth of cells. The method comprises administering a compound of the above formula to a biological system. In particular, the method inhibits the abnormal growth of cells in a mammal such as a human being. Also disclosed is a method of effecting an anti-allergic response by administering the compounds.
Type:
Grant
Filed:
June 15, 1998
Date of Patent:
May 1, 2001
Assignee:
Schering Corporation
Inventors:
Alan B. Cooper, Jagdish A. Desai, Anil K. Saksena, Viyyoor M. Girijavallabhan, James J-S Wang