Search research articles
Contact Us
Filters
Showing results (181-190 of 188) with videos related to
Page
of 19
Sort By:
You have reached the last page of results.
This site can display upto 188 results.
Nature Communications
|
November 30, 2023
Author Correction: A two-dimensional mid-infrared optoelectronic retina enabling simultaneous perception and encoding
Fakun Wang, Fangchen Hu, Mingjin Dai, et al.
Journal of Medicinal Chemistry
|
October 12, 2011
Rational design of phosphoinositide 3-kinase α inhibitors that exhibit selectivity over the phosphoinositide 3-kinase β isoform
Timothy P Heffron, Binqing Wei, Alan Olivero, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 30, 2010
Identification of GNE-477, a potent and efficacious dual PI3K/mTOR inhibitor
Timothy P Heffron, Megan Berry, Georgette Castanedo, et al.
Molecular Cancer Therapeutics
|
July 9, 2009
Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: from PI-103 through PI-540, PI-620 to the oral agent GDC-0941
Florence I Raynaud, Suzanne A Eccles, Sonal Patel, et al.
Journal of Medicinal Chemistry
|
January 7, 2010
Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer
Daniel P Sutherlin, Deepak Sampath, Megan Berry, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 9, 2010
Structure-based optimization of pyrazolo-pyrimidine and -pyridine inhibitors of PI3-kinase
Steven T Staben, Timothy P Heffron, Daniel P Sutherlin, et al.
Journal of Medicinal Chemistry
|
October 11, 2011
Discovery of a potent, selective, and orally available class I phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) kinase inhibitor (GDC-0980) for the treatment of cancer
Daniel P Sutherlin, Linda Bao, Megan Berry, et al.
Journal of Medicinal Chemistry
|
August 30, 2008
The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer
Adrian J Folkes, Khatereh Ahmadi, Wendy K Alderton, et al.
Page
of 19
Search research articles
Search
Showing results (181-190 of 188) with videos related to
Sort By:
Page
of 19
You have reached the last page of results.
This site can display upto 188 results.
Nature Communications
|
November 30, 2023
Author Correction: A two-dimensional mid-infrared optoelectronic retina enabling simultaneous perception and encoding
Fakun Wang, Fangchen Hu, Mingjin Dai, et al.
Journal of Medicinal Chemistry
|
October 12, 2011
Rational design of phosphoinositide 3-kinase α inhibitors that exhibit selectivity over the phosphoinositide 3-kinase β isoform
Timothy P Heffron, Binqing Wei, Alan Olivero, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 30, 2010
Identification of GNE-477, a potent and efficacious dual PI3K/mTOR inhibitor
Timothy P Heffron, Megan Berry, Georgette Castanedo, et al.
Molecular Cancer Therapeutics
|
July 9, 2009
Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: from PI-103 through PI-540, PI-620 to the oral agent GDC-0941
Florence I Raynaud, Suzanne A Eccles, Sonal Patel, et al.
Journal of Medicinal Chemistry
|
January 7, 2010
Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer
Daniel P Sutherlin, Deepak Sampath, Megan Berry, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 9, 2010
Structure-based optimization of pyrazolo-pyrimidine and -pyridine inhibitors of PI3-kinase
Steven T Staben, Timothy P Heffron, Daniel P Sutherlin, et al.
Journal of Medicinal Chemistry
|
October 11, 2011
Discovery of a potent, selective, and orally available class I phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) kinase inhibitor (GDC-0980) for the treatment of cancer
Daniel P Sutherlin, Linda Bao, Megan Berry, et al.
Journal of Medicinal Chemistry
|
August 30, 2008
The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer
Adrian J Folkes, Khatereh Ahmadi, Wendy K Alderton, et al.
Page
of 19