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Journal of Medicinal Chemistry
|
June 1, 2001
Structure-activity studies for a novel series of bicyclic substituted hexahydrobenz[e]isoindole alpha1A adrenoceptor antagonists as potential agents for the symptomatic treatment of benign prostatic hyperplasia
M D Meyer, R J Altenbach, H Bai, et al.
Journal of Medicinal Chemistry
|
October 10, 2008
Discovery of an orally bioavailable small molecule inhibitor of prosurvival B-cell lymphoma 2 proteins
Cheol-Min Park, Milan Bruncko, Jessica Adickes, et al.
Journal of Medicinal Chemistry
|
November 5, 1997
Synthesis and pharmacological characterization of 3-[2-((3aR,9bR)-cis-6-methoxy-2,3,3a,4,5,9b-hexahydro-1H-benz[e] isoindol-2-yl)ethyl]pyrido-[3',4':4,5]thieno[3,2-d]pyrimidine-2,4 (1H,3H)-dione (A-131701): a uroselective alpha 1A adrenoceptor antagonist for the symptomatic treatment of benign prostatic hyperplasia
M D Meyer, R J Altenbach, F Z Basha, et al.
Journal of Medicinal Chemistry
|
February 3, 2006
Discovery and structure-activity relationship of antagonists of B-cell lymphoma 2 family proteins with chemopotentiation activity in vitro and in vivo
Michael D Wendt, Wang Shen, Aaron Kunzer, et al.
Journal of Medicinal Chemistry
|
January 30, 2007
Studies leading to potent, dual inhibitors of Bcl-2 and Bcl-xL
Milan Bruncko, Thorsten K Oost, Barbara A Belli, et al.
Chemical Biology & Drug Design
|
July 17, 2007
Discovery and design of novel HSP90 inhibitors using multiple fragment-based design strategies
Jeffrey R Huth, Chang Park, Andrew M Petros, et al.
Journal of Medicinal Chemistry
|
April 4, 2017
Fragment-Based, Structure-Enabled Discovery of Novel Pyridones and Pyridone Macrocycles as Potent Bromodomain and Extra-Terminal Domain (BET) Family Bromodomain Inhibitors
Le Wang, John K Pratt, Todd Soltwedel, et al.
Science Translational Medicine
|
March 20, 2015
Exploiting selective BCL-2 family inhibitors to dissect cell survival dependencies and define improved strategies for cancer therapy
Joel D Leverson, Darren C Phillips, Michael J Mitten, et al.
Nature
|
May 20, 2005
An inhibitor of Bcl-2 family proteins induces regression of solid tumours
Tilman Oltersdorf, Steven W Elmore, Alexander R Shoemaker, et al.
ACS Medicinal Chemistry Letters
|
October 16, 2020
Discovery of A-1331852, a First-in-Class, Potent, and Orally-Bioavailable BCL-X<sub>L</sub> Inhibitor
Le Wang, George A Doherty, Andrew S Judd, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
Journal of Medicinal Chemistry
|
June 1, 2001
Structure-activity studies for a novel series of bicyclic substituted hexahydrobenz[e]isoindole alpha1A adrenoceptor antagonists as potential agents for the symptomatic treatment of benign prostatic hyperplasia
M D Meyer, R J Altenbach, H Bai, et al.
Journal of Medicinal Chemistry
|
October 10, 2008
Discovery of an orally bioavailable small molecule inhibitor of prosurvival B-cell lymphoma 2 proteins
Cheol-Min Park, Milan Bruncko, Jessica Adickes, et al.
Journal of Medicinal Chemistry
|
November 5, 1997
Synthesis and pharmacological characterization of 3-[2-((3aR,9bR)-cis-6-methoxy-2,3,3a,4,5,9b-hexahydro-1H-benz[e] isoindol-2-yl)ethyl]pyrido-[3',4':4,5]thieno[3,2-d]pyrimidine-2,4 (1H,3H)-dione (A-131701): a uroselective alpha 1A adrenoceptor antagonist for the symptomatic treatment of benign prostatic hyperplasia
M D Meyer, R J Altenbach, F Z Basha, et al.
Journal of Medicinal Chemistry
|
February 3, 2006
Discovery and structure-activity relationship of antagonists of B-cell lymphoma 2 family proteins with chemopotentiation activity in vitro and in vivo
Michael D Wendt, Wang Shen, Aaron Kunzer, et al.
Journal of Medicinal Chemistry
|
January 30, 2007
Studies leading to potent, dual inhibitors of Bcl-2 and Bcl-xL
Milan Bruncko, Thorsten K Oost, Barbara A Belli, et al.
Chemical Biology & Drug Design
|
July 17, 2007
Discovery and design of novel HSP90 inhibitors using multiple fragment-based design strategies
Jeffrey R Huth, Chang Park, Andrew M Petros, et al.
Journal of Medicinal Chemistry
|
April 4, 2017
Fragment-Based, Structure-Enabled Discovery of Novel Pyridones and Pyridone Macrocycles as Potent Bromodomain and Extra-Terminal Domain (BET) Family Bromodomain Inhibitors
Le Wang, John K Pratt, Todd Soltwedel, et al.
Science Translational Medicine
|
March 20, 2015
Exploiting selective BCL-2 family inhibitors to dissect cell survival dependencies and define improved strategies for cancer therapy
Joel D Leverson, Darren C Phillips, Michael J Mitten, et al.
Nature
|
May 20, 2005
An inhibitor of Bcl-2 family proteins induces regression of solid tumours
Tilman Oltersdorf, Steven W Elmore, Alexander R Shoemaker, et al.
ACS Medicinal Chemistry Letters
|
October 16, 2020
Discovery of A-1331852, a First-in-Class, Potent, and Orally-Bioavailable BCL-X<sub>L</sub> Inhibitor
Le Wang, George A Doherty, Andrew S Judd, et al.
Page
of 10