The present invention provides novel compounds useful as proteasome inhibitors. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various diseases.
Certain Substituted Diphenyl Ureas, As Modulators Of Kinase Activity
Scott A. Mitchell - East Haven CT, US Mihaela Diana Danca - Mendham NJ, US Peter A. Blomgren - North Branford CT, US Robert W. DeSimone - Durham CT, US Douglas A. I. Pippin - Chester Springs PA, US
Assignee:
CGI Pharmaceuticals, Inc. - Branford CT
International Classification:
A61K 31/4439 C07D 403/02
US Classification:
514341, 5462727, 5462741
Abstract:
Certain chemical entities chosen from compounds of Formula 1 and pharmaceutically acceptable salts, solvates, crystal forms, chelates, non-covalent complexes, prodrugs, and mixtures thereof, are provided herein. Pharmaceutical compositions comprising at least one chemical entity and one or more pharmaceutically acceptable vehicle chosen from carriers, adjuvants, and excipients, are also provided herein. Methods of treating patients suffering from certain diseases and disorders responsive to angiogenic kinase modulation, which comprise administering to such patients an amount of at least one chemical entity effective to reduce signs or symptoms of the disease or disorder are disclosed. These diseases include cancer, including breast neoplasia, endometrial cancer, colon cancer, and neck squamous cell carcinoma. Methods of treatment include administering at least one chemical entity as a single active agent or administering such at least one chemical entity in combination with one or more other therapeutic agents. A method for determining the presence or absence of an angiogenic kinase in a sample comprising contacting the sample with at least one chemical entity under conditions that permit detection of activity of the angiogenic kinase, detecting a level of the activity of the angiogenic kinase, and therefrom determining the presence or absence of the angiogenic kinase in the sample.
The present invention provides novel compounds useful as proteasome inhibitors. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various diseases.
Certain Substituted Ureas, As Modulators Of Kinase Activity
Scott A. Mitchell - East Haven CT, US Mihaela Diana Danca - Mendham NJ, US Peter A. Blomgren - North Branford CT, US David R. Brittelli - Branford CT, US Pavel Zhichkin - Latham NY, US Matthew E. Voss - Nassau NY, US
Assignee:
CGI Pharmaceuticals, Inc. - Branford CT
International Classification:
C07D 215/38
US Classification:
546167
Abstract:
Certain chemical entities chosen from compounds of Formula 1 and pharmaceutically acceptable salts, solvates, chelates, non-covalent complexes, and prodrugs thereof, are provided herein. Pharmaceutical compositions comprising at least one chemical entity and one or more pharmaceutically acceptable vehicles chosen from carriers, adjuvants, and excipients, are also provided herein. Methods of treating patients suffering from certain diseases and disorders responsive to angiogenic kinase modulation, which comprise administering to such patients an amount of at least one chemical entity effective to reduce signs or symptoms of the disease or disorder are disclosed. These diseases include cancer, including breast neoplasia, endometrial cancer, colon cancer, and neck squamous cell carcinoma. Methods of treatment include administering at least one chemical entity as a single active agent or administering such at least one chemical entity in combination with one or more other therapeutic agents. A method for determining the presence or absence of an angiogenic kinase in a sample comprising contacting the sample with at least one chemical entity under conditions that permit detection of activity of the angiogenic kinase, detecting a level of the activity of the angiogenic kinase, and therefrom determining the presence or absence of the angiogenic kinase in the sample.
Tricia J. Vos - Medford MA, US Michael Patane - Andover MA, US Michael E. Solomon - Concord MA, US Christopher Blackburn - Natick MA, US Mihaela D. Danca - Belmont MA, US
This invention provides compounds and methods for treating melanocortin receptor associated disorders, such as weight loss disorders including cachexia resulting from cancer and other chronic illnesses. The compounds are represented by formula I:.
The present invention provides novel compounds useful as proteasome inhibitors. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various diseases.
1H-Indazoles, Benzothiazoles, 1,2-Benzoisoxazoles, 1,2-Benzoisothiazoles, And Chromones And Preparation And Uses Thereof
Richard Schumacher - Monroe NY, US Jianguo Ma - Natick MA, US Brian Herbert - Stockholm NJ, US Mihaela Diana Danca - Mendham NJ, US Wenge Xie - Mahwah NJ, US Truc Minh Nguyen - New York NY, US Ashok Tehim - Ridgewood NJ, US
Assignee:
Memory Pharmaceuticals Corporation - Montvale NJ
International Classification:
A61P 25/28 A61K 31/551 C07D 487/08
US Classification:
514219, 514221, 540556
Abstract:
The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.
Tricia J. Vos - Medford MA, US Michael Patane - Andover MA, US Michael E. Solomon - Concord MA, US Christopher Blackburn - Natick MA, US Mihaela D. Danca - Belmont MA, US
This invention provides compounds and methods for treating melanocortin receptor associated disorders, such as weight loss disorders including cachexia resulting from cancer and other chronic illnesses. The compounds are represented by formula I:.
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