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Publications by Rachel M. Lanigan
Pyrido[3,4-D]pyrimidin-4(3h)-One Metabolism Mediated by Aldehyde Oxidase Is Blocked by C2-Substitution
Xenobiotica
Pharmacology
Biochemistry
Mutagenesis
Health
Medicine
Toxicology
Related publications
8-Substituted Pyrido[3,4-D]pyrimidin-4(3h)-One Derivatives as Potent, Cell Permeable, KDM4 (JMJD2) and KDM5 (JARID1) Histone Lysine Demethylase Inhibitors
Anticancer Activity Evaluation of New Thieno[2,3-D]pyrimidin-4(3h)-Ones and Thieno[3,2-D]pyrimidin-4(3h)-One Derivatives
Scientia Pharmaceutica
Pharmaceutical Science
Synthesis and Antibacterial Activity of a New Series of 2,3,5,7-Substituted-Pyrido[2,3-D]pyrimidin-4(3h)-One Derivatives
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
3-(4-Chlorophenyl)-2-(Diisopropylamino)-1-Benzofuro[3,2-D]pyrimidin-4(3h)-One
Acta Crystallographica Section E Structure Reports Online
2-(2-Hydroxyethylamino)-3-Phenyl-1-Benzofuro[3,2-D]pyrimidin-4(3h)-One Dichloromethane Hemisolvate
Acta Crystallographica Section E Structure Reports Online
HNF-4 -Mediated Hepatocyte Differentiation Is Blocked by Mutant IDH
Cancer Discovery
Oncology
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4d]pyrimidin-4(3H)one Derivatives
2-(Dibutylamino)-3-(4-Fluorophenyl)-5,6,7,8-Tetrahydro-7-Methyl-6,8-Diphenylpyridine[3′,4′:2,3]thieno[5,4-D]pyrimidin-4(3h)-One
Acta Crystallographica Section E Structure Reports Online
6-(4-Chlorophenyl)-3-Substituted-Thieno[3, 2-D]pyrimidin-4(3h)-One-Based Melanin-Concentrating Hormone Receptor 1 Antagonist
