Steven L. Bender - Oceanside CA Arlindo L. Castelhano - New City NY Wesley K. M. Chong - Encinitas CA Melwyn A. Abreo - Imperial Beach CA Roland J. Billedeau - Santa Clara CA Jian Jeffrey Chen - Santa Clara CA Judith G. Deal - Temecula CA
Assignee:
Agouron Pharmaceuticals Inc. - La Jolla CA
International Classification:
C07D23354
US Classification:
5483361, 548215, 5483381, 5483751, 540524
Abstract:
The present invention is directed to compound of the formula I: wherein R , R , R , R , R , X, Y, and are as defined herein. These compounds are useful for inhibiting the activity of a metalloproteinase by contacting the metalloproteinase with an effective amount of the inventive compounds.
Amide Compounds And Pharmaceutical Compositions For Inhibiting Protein Kinases, And Methods For Their Use
Steven Lee Bender - Oceanside CA Dilip Bhumralkar - San Diego CA Michael Raymond Collins - San Diego CA Stephen James Cripps - San Diego CA Judith Gail Deal - Wildomar CA Lei Jia - San Diego CA Mitchell David Nambu - San Diego CA Cynthia Louise Palmer - La Mesa CA Zhengwei Peng - San Diego CA Michael David Varney - Solana Beach CA
Amide compounds represented by the formula: wherein: R is a moiety represented by the formula âwhere X is selected from the group consisting of CH , O, S, and NH; and Y is selected from the group consisting of CH , O, and S, provided that at least one of X and Y is CH , or X and Y together with the bond there-between form a cyclopropyl; are described. These compounds and pharmaceutical compositions containing them modulate and/or inhibit the activity of certain protein kinases and are capable of mediating tyrosine kinase signal transduction in order to modulate and/or inhibit unwanted cell proliferation. The invention is also directed to the therapeutic or prophylactic use of pharmaceutical compositions containing such compounds, and to methods of treating cancer as well as other disease states associated with unwanted angiogenesis and/or cellular proliferation, such as diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, and psoriasis, by administering effective amounts of such compounds.
Benzofused Heterozryl Amide Derivatives Of Thienopyridines Useful As Therapeutic Agents, Pharmaceutical Compositions Including The Same, And Methods For Their Use
Michael Collins - San Diego CA, US Stephan Cripps - San Diego CA, US Judith Deal - Wildomar CA, US Robert Steven Kania - San Diego CA, US Jihong Lou - San Diego CA, US Mingying He - San Diego CA, US Cynthia Louise Palmer - La Mesa CA, US Ru Zhou - Carlsbad CA, US
Assignee:
Agouron Pharmaceuticals, Inc. - La Jolla CA
International Classification:
A61K031/4365 C07D495/04 C07D409/14
US Classification:
514301, 546114
Abstract:
The invention relates to compounds represented by the formula I and to prodrugs or metabolites thereof, or pharmaceutically acceptable salts or solvates of said compounds, said prodrugs, and said metabolites, wherein Z, Y, Rand R, R, R, and Rare as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula I and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formula I.
Benzofused Heterozryl Amide Derivatives Of Thienopyridines Useful As Therapeutic Agents, Pharmaceutical Compositions Including The Same, And Methods For Their Use
Michael Collins - San Diego CA, US Stephan Cripps - San Diego CA, US Judith Deal - Wildomar CA, US Robert Steven Kania - San Diego CA, US Jihong Lou - San Diego CA, US Mingying He - San Diego CA, US Cynthia Louise Palmer - La Mesa CA, US Ru Zhou - Carlsbad CA, US
Jingrong Jean Cui - San Diego CA, US Judith Gail Deal - Wildomar CA, US Danlin Gu - San Diego CA, US Chuangxing Guo - San Diego CA, US Mary Catherine Johnson - San Diego CA, US Robert Steven Kania - San Diego CA, US Susan Elizabeth Kephart - San Diego CA, US Maria Angelica Linton - San Diego CA, US Indrawan James McAlpine - San Diego CA, US Mason Alan Pairish - San Diego CA, US Cynthia Louise Palmer - La Mesa CA, US
Assignee:
Pfizer Inc. - New York NY
International Classification:
A61K 31/505
US Classification:
514275, 544331, 546113, 5483731
Abstract:
The present invention is directed to compounds of Formula (I),.
Amide Compounds And Pharmaceutical Compositions For Inhibiting Protein Kinases, And Methods For Their Use
Steven Bender - Oceanside CA, US Michael Collins - San Diego CA, US Stephen Cripps - San Diego CA, US Judith Deal - Wildomar CA, US Lei Jia - San Diego CA, US Mitchell Nambu - San Diego CA, US Cynthia Palmer - La Mesa CA, US Zhengwei Peng - San Diego CA, US Michael Varney - Solana Beach CA, US
International Classification:
C07D271/12 C07D285/14 C07D249/08
US Classification:
548/131000, 548/136000, 548/262200
Abstract:
Amide compounds that modulate and/or inhibit the activity of certain protein kinases are described. These compounds and pharmaceutical compositions containing them are capable of mediating tyrosine kinase signal transduction in order to modulate and/or inhibit unwanted cell proliferation. The invention is also directed to the therapeutic or prophylactic use of pharmaceutical compositions containing such compounds, and to methods of treating cancer as well as other disease states associated with unwanted angiogenesis and/or cellular proliferation, such as diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, and psoriasis, by administering effective amounts of such compounds.
3,5 Disubstituted Indazole Compounds With Nitrogen-Bearing 5-Membered Heterocycles, Pharmaceutical Compositions, And Methods For Mediating Or Inhibiting Cell Proliferation
Indrawan McAlpine - San Diego CA, US Judith Deal - Wildomar CA, US Mary Johnson - San Diego CA, US Susan Kephart - San Diego CA, US Julie Park - Cambridge MA, US William Romines - San Diego CA, US Jayashree Tikhe - San Diego CA, US
International Classification:
A61K031/4439 C07D043/14
US Classification:
514338000, 546268100
Abstract:
3,5 disubstituted indazole compounds with substituted nitrogen bearing 5-membered heterocycles in the 3-position that modulate and/or inhibit cell proliferation, such as the activity of protein kinases are described. These compounds and pharmaceutical compositions containing them are capable of mediating CDK dependent diseases to modulate and/or inhibit unwanted cell proliferation. The invention is also directed to the therapeutic or prophylactic use of pharmaceutical compositions containing such compounds, and to methods of treating cancer as well as other disease states associated with unwanted angiogenesis and/or cellular proliferation, such as diabetic retinopathy, neovascular glaucoma, rheumatoid arthritis, and psoriasis, by administering effective amounts of such compounds.
Benzofused Heterozryl Amide Derivatives Of Thienopyridines Useful As Therapeutic Agents, Pharmaceutical Compositions Including The Same, And Methods For Their Use
Michael Collins - San Diego CA, US Stephan Cripps - San Diego CA, US Judith Deal - Wildomar CA, US Robert Kania - San Diego CA, US Jihong Lou - San Diego CA, US Mingying He - San Diego CA, US Cynthia Palmer - La Mesa CA, US William Romines - San Diego CA, US Ru Zhou - Carlsbad CA, US
International Classification:
A61K 31/4743 C07D 498/02
US Classification:
514301000, 546114000
Abstract:
The invention relates to compounds represented by the formula I and to prodrugs or metabolites thereof, or pharmaceutically acceptable salts or solvates of said compounds, said prodrugs, and said metabolites, wherein Z, Y, Rand R, R, R, and Rare as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula I and to methods of treating hyperproliferative disorders in a mammal by administering the compounds of formula I.
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