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Anne M Hassell

Showing results (11-20 of 16) with videos related to

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Acta Crystallographica. Section D, Biological Crystallography|December 14, 2006
Crystallization of protein-ligand complexesAnne M Hassell, Gang An, Randy K Bledsoe, et al.
Bioorganic & Medicinal Chemistry Letters|December 6, 2008
Discovery of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidines: potent inhibitors of the IGF-1R receptor tyrosine kinaseStanley D Chamberlain, Joseph W Wilson, Felix Deanda, et al.
Bioorganic & Medicinal Chemistry Letters|December 17, 2008
Optimization of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivityStanley D Chamberlain, Anikó M Redman, Joseph W Wilson, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2005
P2-P3 conformationally constrained ketoamide-based inhibitors of cathepsin KDavid G Barrett, Virginia M Boncek, John G Catalano, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2008
6-Ethynylthieno[3,2-d]- and 6-ethynylthieno[2,3-d]pyrimidin-4-anilines as tunable covalent modifiers of ErbB kinasesEdgar R Wood, Lisa M Shewchuk, Byron Ellis, et al.
Bioorganic & Medicinal Chemistry Letters|December 23, 2008
Discovery and optimization of imidazo[1,2-a]pyridine inhibitors of insulin-like growth factor-1 receptor (IGF-1R)Kyle A Emmitte, Brian J Wilson, Erich W Baum, et al.
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Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Acta Crystallographica. Section D, Biological Crystallography|December 14, 2006
Crystallization of protein-ligand complexesAnne M Hassell, Gang An, Randy K Bledsoe, et al.
Bioorganic & Medicinal Chemistry Letters|December 6, 2008
Discovery of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidines: potent inhibitors of the IGF-1R receptor tyrosine kinaseStanley D Chamberlain, Joseph W Wilson, Felix Deanda, et al.
Bioorganic & Medicinal Chemistry Letters|December 17, 2008
Optimization of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivityStanley D Chamberlain, Anikó M Redman, Joseph W Wilson, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2005
P2-P3 conformationally constrained ketoamide-based inhibitors of cathepsin KDavid G Barrett, Virginia M Boncek, John G Catalano, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2008
6-Ethynylthieno[3,2-d]- and 6-ethynylthieno[2,3-d]pyrimidin-4-anilines as tunable covalent modifiers of ErbB kinasesEdgar R Wood, Lisa M Shewchuk, Byron Ellis, et al.
Bioorganic & Medicinal Chemistry Letters|December 23, 2008
Discovery and optimization of imidazo[1,2-a]pyridine inhibitors of insulin-like growth factor-1 receptor (IGF-1R)Kyle A Emmitte, Brian J Wilson, Erich W Baum, et al.
Pageof 2