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Bioorganic & Medicinal Chemistry
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March 1, 2011
Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells
Mi-hyun Kim, Minjung Kim, Hana Yu, et al.
International Journal of Molecular Sciences
|
April 30, 2021
Novel and Potent Small Molecules against Melanoma Harboring BRAF Class I/II/III Mutants for Overcoming Drug Resistance
Namkyoung Kim, Injae Shin, Jiwon Lee, et al.
European Journal of Medicinal Chemistry
|
May 20, 2011
Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines
Mohammed I El-Gamal, Myung-Ho Jung, Woong San Lee, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 19, 2017
Characterization of a highly selective inhibitor of the Aurora kinases
Fleur M Ferguson, Zainab M Doctor, Apirat Chaikuad, et al.
ACS Medicinal Chemistry Letters
|
May 19, 2016
Discovery of a Highly Potent and Selective Indenoindolone Type 1 Pan-FLT3 Inhibitor
John M Hatcher, Ellen Weisberg, Taebo Sim, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 1, 2012
Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines. Part 2
Myung-Ho Jung, Mohammed I El-Gamal, Mohammed S Abdel-Maksoud, et al.
Chemical Biology & Drug Design
|
October 21, 2017
Amphiphilic small peptides for delivery of plasmid DNAs and siRNAs
Eun-Kyoung Bang, Hanna Cho, Sean S-H Jeon, et al.
The Journal of Organic Chemistry
|
September 14, 2017
Structural Revision of Baulamycin A and Structure-Activity Relationships of Baulamycin A Derivatives
Sandip Sengupta, Munhyung Bae, Dong-Chan Oh, et al.
ACS Medicinal Chemistry Letters
|
March 18, 2011
Discovery of a benzo[e]pyrimido-[5,4-b][1,4]diazepin-6(11H)-one as a Potent and Selective Inhibitor of Big MAP Kinase 1
Xianming Deng, Qingkai Yang, Nicholas Kwiatkowski, et al.
Cellular Signalling
|
February 17, 2015
Non-receptor tyrosine kinase inhibitors enhances β-cell survival by suppressing the PKCδ signal transduction pathway in streptozotocin-induced β-cell apoptosis
Udayakumar Karunakaran, Si Jun Park, Do Youn Jun, et al.
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of 13
Search research articles
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Showing results (31-40 of 121) with videos related to
Sort By:
Page
of 13
Bioorganic & Medicinal Chemistry
|
March 1, 2011
Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells
Mi-hyun Kim, Minjung Kim, Hana Yu, et al.
International Journal of Molecular Sciences
|
April 30, 2021
Novel and Potent Small Molecules against Melanoma Harboring BRAF Class I/II/III Mutants for Overcoming Drug Resistance
Namkyoung Kim, Injae Shin, Jiwon Lee, et al.
European Journal of Medicinal Chemistry
|
May 20, 2011
Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines
Mohammed I El-Gamal, Myung-Ho Jung, Woong San Lee, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 19, 2017
Characterization of a highly selective inhibitor of the Aurora kinases
Fleur M Ferguson, Zainab M Doctor, Apirat Chaikuad, et al.
ACS Medicinal Chemistry Letters
|
May 19, 2016
Discovery of a Highly Potent and Selective Indenoindolone Type 1 Pan-FLT3 Inhibitor
John M Hatcher, Ellen Weisberg, Taebo Sim, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 1, 2012
Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines. Part 2
Myung-Ho Jung, Mohammed I El-Gamal, Mohammed S Abdel-Maksoud, et al.
Chemical Biology & Drug Design
|
October 21, 2017
Amphiphilic small peptides for delivery of plasmid DNAs and siRNAs
Eun-Kyoung Bang, Hanna Cho, Sean S-H Jeon, et al.
The Journal of Organic Chemistry
|
September 14, 2017
Structural Revision of Baulamycin A and Structure-Activity Relationships of Baulamycin A Derivatives
Sandip Sengupta, Munhyung Bae, Dong-Chan Oh, et al.
ACS Medicinal Chemistry Letters
|
March 18, 2011
Discovery of a benzo[e]pyrimido-[5,4-b][1,4]diazepin-6(11H)-one as a Potent and Selective Inhibitor of Big MAP Kinase 1
Xianming Deng, Qingkai Yang, Nicholas Kwiatkowski, et al.
Cellular Signalling
|
February 17, 2015
Non-receptor tyrosine kinase inhibitors enhances β-cell survival by suppressing the PKCδ signal transduction pathway in streptozotocin-induced β-cell apoptosis
Udayakumar Karunakaran, Si Jun Park, Do Youn Jun, et al.
Page
of 13