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Identification of a selective inhibitor of human monocarboxylate transporter 4. , Futagi Y., Biochem Biophys Res Commun. January 1, 2018; 495 (1): 427-432.
The anti-tumour agent lonidamine is a potent inhibitor of the mitochondrial pyruvate carrier and plasma membrane monocarboxylate transporters. , Nancolas B., Biochem J. April 1, 2016; 473 (7): 929-36.
Identification of key binding site residues of MCT1 for AR-C155858 reveals the molecular basis of its isoform selectivity. , Nancolas B., Biochem J. February 15, 2015; 466 (1): 177-88.
The inhibition of monocarboxylate transporter 2 ( MCT2) by AR-C155858 is modulated by the associated ancillary protein. , Ovens MJ., Biochem J. October 15, 2010; 431 (2): 217-25.
AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that binds to an intracellular site involving transmembrane helices 7-10. , Ovens MJ., Biochem J. January 15, 2010; 425 (3): 523-30.
The role of charged residues in the transmembrane helices of monocarboxylate transporter 1 and its ancillary protein basigin in determining plasma membrane expression and catalytic activity. , Manoharan C., Mol Membr Biol. January 1, 2006; 23 (6): 486-98.