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Journal of Medicinal Chemistry
|
September 9, 2015
Identification of Substituted Naphthotriazolediones as Novel Tryptophan 2,3-Dioxygenase (TDO) Inhibitors through Structure-Based Virtual Screening
Jian-Sung Wu, Shu-Yu Lin, Fang-Yu Liao, et al.
Bioorganic & Medicinal Chemistry
|
April 27, 2013
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Wen-Hsing Lin, John T-A Hsu, Shu-Yi Hsieh, et al.
Journal of Medicinal Chemistry
|
June 17, 2010
Fast-forwarding hit to lead: aurora and epidermal growth factor receptor kinase inhibitor lead identification
Mohane Selvaraj Coumar, Chang-Ying Chu, Cheng-Wei Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 24, 2013
Aurora kinase inhibitors reveal mechanisms of HURP in nucleation of centrosomal and kinetochore microtubules
Jiun-Ming Wu, Chiung-Tong Chen, Mohane Selvaraj Coumar, et al.
Antimicrobial Agents and Chemotherapy
|
December 3, 1998
ABT-378, a highly potent inhibitor of the human immunodeficiency virus protease
H L Sham, D J Kempf, A Molla, et al.
Communications Earth & Environment
|
March 18, 2025
Integrated fire management as an adaptation and mitigation strategy to altered fire regimes
I Oliveras Menor, N Prat-Guitart, G L Spadoni, et al.
Journal of Medicinal Chemistry
|
October 22, 2010
Design and synthesis of tetrahydropyridothieno[2,3-d]pyrimidine scaffold based epidermal growth factor receptor (EGFR) kinase inhibitors: the role of side chain chirality and Michael acceptor group for maximal potency
Chia-Hsien Wu, Mohane Selvaraj Coumar, Chang-Ying Chu, et al.
Oncotarget
|
November 19, 2016
Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluation
Yung Chang Hsu, Mohane Selvaraj Coumar, Wen-Chieh Wang, et al.
Geroscience
|
January 25, 2020
Loss of vacuolar acidity results in iron-sulfur cluster defects and divergent homeostatic responses during aging in Saccharomyces cerevisiae
Kenneth L Chen, Toby N Ven, Matthew M Crane, et al.
Applied Biochemistry and Biotechnology
|
November 16, 2013
Patents and literature
A Rembaum, R P Rohrbach, S Klose, et al.
Page
of 37
Search research articles
Search
Showing results (351-360 of 361) with videos related to
Sort By:
Page
of 37
Journal of Medicinal Chemistry
|
September 9, 2015
Identification of Substituted Naphthotriazolediones as Novel Tryptophan 2,3-Dioxygenase (TDO) Inhibitors through Structure-Based Virtual Screening
Jian-Sung Wu, Shu-Yu Lin, Fang-Yu Liao, et al.
Bioorganic & Medicinal Chemistry
|
April 27, 2013
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
Wen-Hsing Lin, John T-A Hsu, Shu-Yi Hsieh, et al.
Journal of Medicinal Chemistry
|
June 17, 2010
Fast-forwarding hit to lead: aurora and epidermal growth factor receptor kinase inhibitor lead identification
Mohane Selvaraj Coumar, Chang-Ying Chu, Cheng-Wei Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 24, 2013
Aurora kinase inhibitors reveal mechanisms of HURP in nucleation of centrosomal and kinetochore microtubules
Jiun-Ming Wu, Chiung-Tong Chen, Mohane Selvaraj Coumar, et al.
Antimicrobial Agents and Chemotherapy
|
December 3, 1998
ABT-378, a highly potent inhibitor of the human immunodeficiency virus protease
H L Sham, D J Kempf, A Molla, et al.
Communications Earth & Environment
|
March 18, 2025
Integrated fire management as an adaptation and mitigation strategy to altered fire regimes
I Oliveras Menor, N Prat-Guitart, G L Spadoni, et al.
Journal of Medicinal Chemistry
|
October 22, 2010
Design and synthesis of tetrahydropyridothieno[2,3-d]pyrimidine scaffold based epidermal growth factor receptor (EGFR) kinase inhibitors: the role of side chain chirality and Michael acceptor group for maximal potency
Chia-Hsien Wu, Mohane Selvaraj Coumar, Chang-Ying Chu, et al.
Oncotarget
|
November 19, 2016
Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluation
Yung Chang Hsu, Mohane Selvaraj Coumar, Wen-Chieh Wang, et al.
Geroscience
|
January 25, 2020
Loss of vacuolar acidity results in iron-sulfur cluster defects and divergent homeostatic responses during aging in Saccharomyces cerevisiae
Kenneth L Chen, Toby N Ven, Matthew M Crane, et al.
Applied Biochemistry and Biotechnology
|
November 16, 2013
Patents and literature
A Rembaum, R P Rohrbach, S Klose, et al.
Page
of 37