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Publications by Sarah Kado
Activation of the Aryl Hydrocarbon Receptor by the Widely Used SRC Family Kinase Inhibitor 4-Amino-5-(4-Chlorophenyl)-7-(Dimethylethyl)pyrazolo[3,4-D]pyrimidine (PP2)
Archives of Toxicology
Mutagenesis
Toxicology
Health
Medicine
Related publications
Studies on Pyrazolo(3,4-D)pyrimidine Derivatives. XIII. Aryl Migration of 4-Aroyl-1h-Pyrazolo(3,4-D)pyrimidines to 4-Aryl-4,5-Dihydro-1h-Pyrazolo(3,4-D)pyrimidine-4-Carboxylic Acids.
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
4-(Prop-2-Yn-1-Ylsulfanyl)-1h-Pyrazolo[3,4-D]pyrimidine
IUCrData
Crystal Structure of 1-Methyl-4-Methylsulfanyl-1h-Pyrazolo[3,4-D]pyrimidine
Acta Crystallographica Section E Structure Reports Online
Studies on Pyrazolo[3, 4-D]pyrimidine Derivatives.III. On the Reaction of 1-Methyl-And 1-Phenyl-4-Chloro-1h-Pyrazolo[3, 4-D]-Pyrimidine With Carbanion
Yakugaku Zasshi
Pharmacology
Pharmaceutical Science
Synthesis of Some Novel Pyrazolo[3,4-D]pyrimidine Derivatives
Arkivoc
Organic Chemistry
Studies on Pyrazolo [3, 4-D] Pyrimidine Derivatives. I. On the Reactions of 1-Methyl-And 1-Phenyl-1h-Pyrazolo-[3, 4-D] Pyrimidine With Grignard Reagent
Yakugaku Zasshi
Pharmacology
Pharmaceutical Science
5-Butylamino-6-(4-Fluorophenyl)-7-Oxo-1-P-Tolyl-6,7-Dihydro-1h-Pyrazolo[4,3-D]pyrimidine-3-Carbonitrile
Acta Crystallographica Section E Structure Reports Online
Synthesis and SRC Kinase Inhibitory Activity of a Series of 4-[(2, 4-Dichloro-5-Methoxyphenyl)amino]-7-Furyl-3-Quinolinecarbonitriles
Ethyl 3-(4-Fluorophenyl)-6-Methyl-4-Oxo-2-(1-Cyclohexylamino)-3,4-Dihydrofuro[2,3-D]pyrimidine-5-Carboxylate
Acta Crystallographica Section E Structure Reports Online
