The present invention relates to novel 3-(cycloalkano-heteroarylidenyl)-2-indolinone compounds and physiologically acceptable salts and prodrugs thereof which are expected to modulate the activity of protein tyrosine kinases and therefore to be useful in the prevention and treatment of protein tyrosine kinase related cellular disorders such as cancer.
Mono- And Bis-Indolylquinones And Prophylactic And Therapeutic Uses Thereof
Peng Cho Tang - Moraga CA 94556 Gerald McMahon - San Francisco CA 94109 Ken Lipson - San Mateo CA 94402
International Classification:
A61K 31404
US Classification:
514414, 548455, 548460
Abstract:
The present invention relates to a class of indolylquinone compounds that inhibit GRB-2 adaptor protein function, pharmaceutical compositions comprising these compounds, and methods for ameliorating the symptoms of cell proliferative disorders associated with GRB-2 adaptor protein function using these compounds. The present invention further relates to methods for treating insulin-related disorders, such as diabetes, insulin resistance, insulin deficiency and insulin allergy, and for ameliorating the symptoms of insulin-related disorders, using certain indolylquinone compounds and pharmaceutical compositions thereof. The present invention also relates to novel synthetic methods for the preparation of mono- and bis-indolylquinone compounds.
Pyrrole Substituted 2-Indolinone Protein Kinase Inhibitors
Peng Cho Tang - Moraga CA Li Sun - Foster City CA Gerald McMahon - Kenwood CA
Assignee:
Sugen, Inc. - South San Francisco CA
International Classification:
A61K 314045
US Classification:
5142352, 514414, 544144, 548468
Abstract:
The present invention relates to novel pyrrole substituted 2-indolinone compounds and physiologically acceptable salts and prodrugs thereof which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.
3-(4²-Bromobenzylindenyl)-2-Indolinone And Analogues Thereof For The Treatment Of Disease
The present invention relates to organic molecules capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.
3-Heteroarylidene-2-Indolinone Protein Kinase Inhibitors
The present invention relates to novel 3-heteroarylidene-2-indolinone compounds and physiologically acceptable salts thereof which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.
3-(Substituted)-2-Indolinones Compounds And Use Thereof As Inhibitors Of Protein Kinase Activity
The present invention relates to novel 3-(substituted)-2-indolinones compounds and physiologically acceptable salts and prodrugs thereof which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related disorders such as cancer.
2-Indolinone Derivatives As Modulators Of Protein Kinase Activity
Peng Cho Tang - Moraga CA Li Sun - Foster City CA Gerald McMahon - Kenwood CA G. David Harris - San Francisco CA
Assignee:
Sugen, Inc. - South San Francisco CA
International Classification:
A61K 31435
US Classification:
514300, 546113, 5483121, 514397
Abstract:
The present invention relates to novel imidazoly 2-indolinones and physiologically acceptable salts and prodrugs thereof which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.
Phosphate Mimics And Methods Of Treatment Using Phosphatase Inhibitors
Ping Huang - Mountain View CA Chung Chen Wei - Foster City CA Peng Cho Tang - Moraga CA Chris Liang - Sunnyvale CA John Ramphal - Union City CA Bahija Jallal - Menlo Park CA John Biltz - Newark CA Sharon Li - Los Altos CA Matt Mattson - Santa Clara CA Gerald McMahon - Kenwood CA Marcel Koenig - Burlingame CA
The invention relates to trifluoromethyl sulfonyl and trifluoromethyl sulfonamido compounds and the physiologically acceptable salts and the prodrugs thereof. These compounds are expected to modulate the activity of protein tyrosine enzymes which are related to cellular signal transduction, in particular, protein tyrosine phosphatase, and therefore are expected to be useful in the prevention and treatment of disorders associated with abnormal protein tyrosine enzyme related cellular signal transduction such as cancer, diabetes, immuno-modulation, neurologic degenerative diseases, osteoporosis and infectious diseases. The invention also relates to the use of compounds containing fluoromethyl sulfonyl groups as phosphate mimics. These mimics may be used to inhibit, regulate or modulate the activity of a phosphate binding protein in a cell.
Dr. McMahon graduated from the SUNY Upstate Medical University in 1986. He works in Syracuse, NY and specializes in Internal Medicine. Dr. McMahon is affiliated with St Josephs Hospital Health Center and Upstate University Hospital Community Campus.
Shenelle Wallace (1989-1993), George Ross (1975-1979), Patty Markham (1961-1965), Frank Smith (1964-1968), Hector Chavez (1971-1975), Gerald McMahon (1957-1961)