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Journal of Medicinal Chemistry
|
April 28, 2006
Structure-based drug design of a novel family of PPARgamma partial agonists: virtual screening, X-ray crystallography, and in vitro/in vivo biological activities
I-Lin Lu, Chien-Fu Huang, Yi-Hui Peng, et al.
Pediatrics
|
March 14, 1998
A phase I/II study of the protease inhibitor ritonavir in children with human immunodeficiency virus infection
B U Mueller, R P Nelson, J Sleasman, et al.
Bioorganic Chemistry
|
March 16, 2020
Drug-like property optimization: Discovery of orally bioavailable quinazoline-based multi-targeted kinase inhibitors
Shu-Yu Lin, Chun-Feng Chang, Mohane Selvaraj Coumar, et al.
Nature Neuroscience
|
March 27, 2012
A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing
Linda Madisen, Tianyi Mao, Henner Koch, et al.
Journal of Medicinal Chemistry
|
February 3, 2006
Indol-1-yl acetic acids as peroxisome proliferator-activated receptor agonists: design, synthesis, structural biology, and molecular docking studies
Neeraj Mahindroo, Chiung-Chiu Wang, Chun-Chen Liao, et al.
Analytical Biochemistry
|
March 25, 2008
A cell-based high-throughput screen for epidermal growth factor receptor pathway inhibitors
Wen-Hsing Lin, Jen-Shin Song, Teng-Yuan Chang, et al.
European Journal of Medicinal Chemistry
|
June 18, 2015
Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations
Chiung-Tong Chen, John T-A Hsu, Wen-Hsing Lin, et al.
Journal of Medicinal Chemistry
|
March 24, 2009
Design and structural analysis of novel pharmacophores for potent and selective peroxisome proliferator-activated receptor gamma agonists
Chia-Hui Lin, Yi-Hui Peng, Mohane Selvaraj Coumar, et al.
Bioorganic & Medicinal Chemistry
|
June 29, 2011
Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Wen-Hsing Lin, Shu-Yi Hsieh, Shih-Chieh Yen, et al.
Journal of Medicinal Chemistry
|
July 2, 2013
Optimization of ligand and lipophilic efficiency to identify an in vivo active furano-pyrimidine Aurora kinase inhibitor
Hui-Yi Shiao, Mohane Selvaraj Coumar, Chun-Wei Chang, et al.
Page
of 37
Search research articles
Search
Showing results (341-350 of 361) with videos related to
Sort By:
Page
of 37
Journal of Medicinal Chemistry
|
April 28, 2006
Structure-based drug design of a novel family of PPARgamma partial agonists: virtual screening, X-ray crystallography, and in vitro/in vivo biological activities
I-Lin Lu, Chien-Fu Huang, Yi-Hui Peng, et al.
Pediatrics
|
March 14, 1998
A phase I/II study of the protease inhibitor ritonavir in children with human immunodeficiency virus infection
B U Mueller, R P Nelson, J Sleasman, et al.
Bioorganic Chemistry
|
March 16, 2020
Drug-like property optimization: Discovery of orally bioavailable quinazoline-based multi-targeted kinase inhibitors
Shu-Yu Lin, Chun-Feng Chang, Mohane Selvaraj Coumar, et al.
Nature Neuroscience
|
March 27, 2012
A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing
Linda Madisen, Tianyi Mao, Henner Koch, et al.
Journal of Medicinal Chemistry
|
February 3, 2006
Indol-1-yl acetic acids as peroxisome proliferator-activated receptor agonists: design, synthesis, structural biology, and molecular docking studies
Neeraj Mahindroo, Chiung-Chiu Wang, Chun-Chen Liao, et al.
Analytical Biochemistry
|
March 25, 2008
A cell-based high-throughput screen for epidermal growth factor receptor pathway inhibitors
Wen-Hsing Lin, Jen-Shin Song, Teng-Yuan Chang, et al.
European Journal of Medicinal Chemistry
|
June 18, 2015
Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations
Chiung-Tong Chen, John T-A Hsu, Wen-Hsing Lin, et al.
Journal of Medicinal Chemistry
|
March 24, 2009
Design and structural analysis of novel pharmacophores for potent and selective peroxisome proliferator-activated receptor gamma agonists
Chia-Hui Lin, Yi-Hui Peng, Mohane Selvaraj Coumar, et al.
Bioorganic & Medicinal Chemistry
|
June 29, 2011
Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Wen-Hsing Lin, Shu-Yi Hsieh, Shih-Chieh Yen, et al.
Journal of Medicinal Chemistry
|
July 2, 2013
Optimization of ligand and lipophilic efficiency to identify an in vivo active furano-pyrimidine Aurora kinase inhibitor
Hui-Yi Shiao, Mohane Selvaraj Coumar, Chun-Wei Chang, et al.
Page
of 37