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D W FRY

Showing results (51-60 of 90) with videos related to

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Cancer Research|March 1, 1985
Enhanced polyglutamylation of aminopterin relative to methotrexate in the Ehrlich ascites tumor cell in vitroL H Matherly, M K Voss, L A Anderson, et al.
Molecular Pharmacology|August 1, 1993
Inhibition of 5-phosphoribosyl-1-pyrophosphate synthetase by the monophosphate metabolite of 4-amino-8-(beta-D-ribofuranosylamino)pyrimido[5,4-d]pyrimidine: a novel mechanism for antitumor activityD W Fry, T J Boritzki, R C Jackson, et al.
Journal of Medicinal Chemistry|March 28, 1997
Structure-based design of a potent, selective, and irreversible inhibitor of the catalytic domain of the erbB receptor subfamily of protein tyrosine kinasesJ Singh, E M Dobrusin, D W Fry, et al.
Clinical and Experimental Pharmacology & Physiology|May 1, 1996
Structure-activity relationships for 4-anilinoquinazolines as potent inhibitors at the ATP binding site of the epidermal growth factor receptor in vitroW A Denny, G W Rewcastle, A J Bridges, et al.
Biochemical Pharmacology|November 1, 1988
Inhibition of type II topoisomerase by fostriecinT J Boritzki, T S Wolfard, J A Besserer, et al.
Anticancer Research|June 16, 1999
Growth inhibition of nasopharyngeal carcinoma cells by EGF receptor tyrosine kinase inhibitorsY Sun, D W Fry, P Vincent, et al.
Journal of Medicinal Chemistry|September 15, 1995
Tyrosine kinase inhibitors. 7. 7-Amino-4-(phenylamino)- and 7-amino-4-[(phenylmethyl)amino]pyrido[4,3-d]pyrimidines: a new class of inhibitors of the tyrosine kinase activity of the epidermal growth factor receptorA M Thompson, A J Bridges, D W Fry, et al.
Journal of Medicinal Chemistry|June 6, 1997
Tyrosine kinase inhibitors. 12. Synthesis and structure-activity relationships for 6-substituted 4-(phenylamino)pyrimido[5,4-d]pyrimidines designed as inhibitors of the epidermal growth factor receptorG W Rewcastle, A J Bridges, D W Fry, et al.
Journal of Medicinal Chemistry|January 20, 2000
Tyrosine kinase inhibitors. 16. 6,5,6-tricyclic benzothieno[3, 2-d]pyrimidines and pyrimido[5,4-b-] and -[4,5-b]ĭndoles as potent inhibitors of the epidermal growth factor receptor tyrosine kinaseH D Showalter, A J Bridges, H Zhou, et al.
Anti-Cancer Drug Design|April 1, 1986
Design, biochemical pharmacology, electrochemistry and tumour biology of anti-tumour anthrapyrazolesH D Showalter, D W Fry, W R Leopold, et al.
Pageof 9

Showing results (51-60 of 90) with videos related to

Sort By:
Pageof 9
Cancer Research|March 1, 1985
Enhanced polyglutamylation of aminopterin relative to methotrexate in the Ehrlich ascites tumor cell in vitroL H Matherly, M K Voss, L A Anderson, et al.
Molecular Pharmacology|August 1, 1993
Inhibition of 5-phosphoribosyl-1-pyrophosphate synthetase by the monophosphate metabolite of 4-amino-8-(beta-D-ribofuranosylamino)pyrimido[5,4-d]pyrimidine: a novel mechanism for antitumor activityD W Fry, T J Boritzki, R C Jackson, et al.
Journal of Medicinal Chemistry|March 28, 1997
Structure-based design of a potent, selective, and irreversible inhibitor of the catalytic domain of the erbB receptor subfamily of protein tyrosine kinasesJ Singh, E M Dobrusin, D W Fry, et al.
Clinical and Experimental Pharmacology & Physiology|May 1, 1996
Structure-activity relationships for 4-anilinoquinazolines as potent inhibitors at the ATP binding site of the epidermal growth factor receptor in vitroW A Denny, G W Rewcastle, A J Bridges, et al.
Biochemical Pharmacology|November 1, 1988
Inhibition of type II topoisomerase by fostriecinT J Boritzki, T S Wolfard, J A Besserer, et al.
Anticancer Research|June 16, 1999
Growth inhibition of nasopharyngeal carcinoma cells by EGF receptor tyrosine kinase inhibitorsY Sun, D W Fry, P Vincent, et al.
Journal of Medicinal Chemistry|September 15, 1995
Tyrosine kinase inhibitors. 7. 7-Amino-4-(phenylamino)- and 7-amino-4-[(phenylmethyl)amino]pyrido[4,3-d]pyrimidines: a new class of inhibitors of the tyrosine kinase activity of the epidermal growth factor receptorA M Thompson, A J Bridges, D W Fry, et al.
Journal of Medicinal Chemistry|June 6, 1997
Tyrosine kinase inhibitors. 12. Synthesis and structure-activity relationships for 6-substituted 4-(phenylamino)pyrimido[5,4-d]pyrimidines designed as inhibitors of the epidermal growth factor receptorG W Rewcastle, A J Bridges, D W Fry, et al.
Journal of Medicinal Chemistry|January 20, 2000
Tyrosine kinase inhibitors. 16. 6,5,6-tricyclic benzothieno[3, 2-d]pyrimidines and pyrimido[5,4-b-] and -[4,5-b]ĭndoles as potent inhibitors of the epidermal growth factor receptor tyrosine kinaseH D Showalter, A J Bridges, H Zhou, et al.
Anti-Cancer Drug Design|April 1, 1986
Design, biochemical pharmacology, electrochemistry and tumour biology of anti-tumour anthrapyrazolesH D Showalter, D W Fry, W R Leopold, et al.
Pageof 9