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Coronary Artery Disease
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July 19, 2013
Bioresorbable polystatin fourth-generation stents
Wayne H Kaesemeyer, Kelly G Sprankle, Jon N Kremsky, et al.
Journal of Medicinal Chemistry
|
December 12, 2003
Structure-based design, synthesis, and antimicrobial activity of indazole-derived SAH/MTA nucleosidase inhibitors
Xiaoming Li, Sam Chu, Victoria A Feher, et al.
Journal of Medicinal Chemistry
|
September 17, 2009
Identification of N-(5-tert-butyl-isoxazol-3-yl)-N'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea dihydrochloride (AC220), a uniquely potent, selective, and efficacious FMS-like tyrosine kinase-3 (FLT3) inhibitor
Qi Chao, Kelly G Sprankle, Robert M Grotzfeld, et al.
Blood
|
August 6, 2009
AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML)
Patrick P Zarrinkar, Ruwanthi N Gunawardane, Merryl D Cramer, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 4, 2009
Arylcarboxyamino-substituted diaryl ureas as potent and selective FLT3 inhibitors
Hitesh K Patel, Robert M Grotzfeld, Andiliy G Lai, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 3, 2011
4-Quinazolinyloxy-diaryl ureas as novel BRAFV600E inhibitors
Mark W Holladay, Brian T Campbell, Martin W Rowbottom, et al.
Journal of Medicinal Chemistry
|
December 16, 2011
Identification of 1-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)-3-(5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-yl)urea hydrochloride (CEP-32496), a highly potent and orally efficacious inhibitor of V-RAF murine sarcoma viral oncogene homologue B1 (BRAF) V600E
Martin W Rowbottom, Raffaella Faraoni, Qi Chao, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Coronary Artery Disease
|
July 19, 2013
Bioresorbable polystatin fourth-generation stents
Wayne H Kaesemeyer, Kelly G Sprankle, Jon N Kremsky, et al.
Journal of Medicinal Chemistry
|
December 12, 2003
Structure-based design, synthesis, and antimicrobial activity of indazole-derived SAH/MTA nucleosidase inhibitors
Xiaoming Li, Sam Chu, Victoria A Feher, et al.
Journal of Medicinal Chemistry
|
September 17, 2009
Identification of N-(5-tert-butyl-isoxazol-3-yl)-N'-{4-[7-(2-morpholin-4-yl-ethoxy)imidazo[2,1-b][1,3]benzothiazol-2-yl]phenyl}urea dihydrochloride (AC220), a uniquely potent, selective, and efficacious FMS-like tyrosine kinase-3 (FLT3) inhibitor
Qi Chao, Kelly G Sprankle, Robert M Grotzfeld, et al.
Blood
|
August 6, 2009
AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML)
Patrick P Zarrinkar, Ruwanthi N Gunawardane, Merryl D Cramer, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 4, 2009
Arylcarboxyamino-substituted diaryl ureas as potent and selective FLT3 inhibitors
Hitesh K Patel, Robert M Grotzfeld, Andiliy G Lai, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 3, 2011
4-Quinazolinyloxy-diaryl ureas as novel BRAFV600E inhibitors
Mark W Holladay, Brian T Campbell, Martin W Rowbottom, et al.
Journal of Medicinal Chemistry
|
December 16, 2011
Identification of 1-(3-(6,7-dimethoxyquinazolin-4-yloxy)phenyl)-3-(5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-yl)urea hydrochloride (CEP-32496), a highly potent and orally efficacious inhibitor of V-RAF murine sarcoma viral oncogene homologue B1 (BRAF) V600E
Martin W Rowbottom, Raffaella Faraoni, Qi Chao, et al.
Page
of 1