Synthesis and structure-activity studies of a series of [(hydroxybenzyl) amino] salicylates as inhibitors of EGF receptor-associated tyrosine kinase activity

H Chen, J Boiziau, F Parker, R Maroun…

Index: Journal of Medicinal Chemistry, , vol. 36, # 25 p. 4094 - 4098

Full Text: HTML

Citation Number: 32

Abstract

... The tyrosine kinase inhibitory potency of these compounds was measured in vitro using ER 22 cell membranes as an 0 1993 American Chemical Society Page 2. [(Hydroxybenzyl) aminolsalicylates OaSO A ... Journal of Medicinal Chemistry, 1993, Vol. 36, No. 25 40915 ...

Related Articles:

Strategic studies in the syntheses of novel 6, 7-substituted quinolones and 7-or 6-substituted 1, 6-and 1, 7-naphthyridones

[Morgentin, Remy; Pasquet, Georges; Boutron, Pascal; Jung, Frederic; Lamorlette, Maryannick; Maudet, Mickael; Ple, Patrick Tetrahedron, 2008 , vol. 64, # 12 p. 2772 - 2782]

Electrochemical C–H amination: Synthesis of aromatic primary amines via N-arylpyridinium ions

[Journal of the American Chemical Society, , vol. 135, # 13 p. 5000 - 5003]

1, 5-Biaryl pyrrole derivatives as EP 1 receptor antagonists. Structure–activity relationships of 6-substituted and 5, 6-disubstituted benzoic acid derivatives

[Bioorganic and Medicinal Chemistry Letters, , vol. 17, # 4 p. 916 - 920]

More Articles...