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Journal of Medicinal Chemistry
|
September 16, 2005
Thienopyrimidine ureas as novel and potent multitargeted receptor tyrosine kinase inhibitors
Yujia Dai, Yan Guo, Robin R Frey, et al.
Journal of Medicinal Chemistry
|
March 9, 2007
Discovery of N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-aminoindazole-based orally active multitargeted receptor tyrosine kinase inhibitor
Yujia Dai, Kresna Hartandi, Zhiqin Ji, et al.
Nature Chemical Biology
|
January 24, 2017
The SUV4-20 inhibitor A-196 verifies a role for epigenetics in genomic integrity
Kenneth D Bromberg, Taylor R H Mitchell, Anup K Upadhyay, et al.
Journal of Medicinal Chemistry
|
September 16, 2024
Discovery of A-910, a Highly Potent and Orally Bioavailable Dual MerTK/Axl-Selective Tyrosine Kinase Inhibitor
Yiyun Yu, Miyeon Jang, Julie Miyashiro, et al.
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of 4
Search research articles
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Showing results (31-40 of 34) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 34 results.
Journal of Medicinal Chemistry
|
September 16, 2005
Thienopyrimidine ureas as novel and potent multitargeted receptor tyrosine kinase inhibitors
Yujia Dai, Yan Guo, Robin R Frey, et al.
Journal of Medicinal Chemistry
|
March 9, 2007
Discovery of N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-aminoindazole-based orally active multitargeted receptor tyrosine kinase inhibitor
Yujia Dai, Kresna Hartandi, Zhiqin Ji, et al.
Nature Chemical Biology
|
January 24, 2017
The SUV4-20 inhibitor A-196 verifies a role for epigenetics in genomic integrity
Kenneth D Bromberg, Taylor R H Mitchell, Anup K Upadhyay, et al.
Journal of Medicinal Chemistry
|
September 16, 2024
Discovery of A-910, a Highly Potent and Orally Bioavailable Dual MerTK/Axl-Selective Tyrosine Kinase Inhibitor
Yiyun Yu, Miyeon Jang, Julie Miyashiro, et al.
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of 4