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H., Murphy, D
De Novo Design of N-(Pyridin-4-Ylmethyl)Aniline Derivatives as KDR Inhibitors: 3D-QSAR, Molecular Fragment Replacement, Protein-Ligand Interaction Fingerprint, and ADMET Prediction
Metabolomics studies have the ability to combine new techniques to stabilize cysteine and interrogate metabolic states within cancer cells
Tumor-targeted inhibition of monocarboxylate transporter 1 improves T-cell immunotherapy of solid tumors
Evidence suggests that valproate, used as a mood stabilizer, is a substrate of OAT1 and homovanillic acid, a metabolite of dopamine, is a substrate of OAT3 (Sekine et al., 2000
