| Literature DB >> 27347360 |
Reji N Nair1, Jitendra K Mishra1, Fangzheng Li1, Mariola Tortosa1, Chunying Yang2, Joanne R Doherty3, Michael Cameron4, John L Cleveland2, William R Roush1, Thomas D Bannister1.
Abstract
Glutamine and tyrosine-based amino acid conjugates of monocarboxylate transporter types 1 and 2 inhibitors (MCT1/2) were designed, synthesized and evaluated for their potency in blocking the proliferation of a human B lymphoma cell line that expresses the transporters Asct2, LAT1 and MCT1. Appropriate placement of an amino acid transporter recognition element was shown to augment anti-tumour efficacy vs. Raji cells. Amino acid conjugation also improves the pharmacodynamic properties of experimental MCT1/2 inhibitors.Entities:
Year: 2016 PMID: 27347360 PMCID: PMC4917231 DOI: 10.1039/C5MD00579E
Source DB: PubMed Journal: Medchemcomm ISSN: 2040-2503 Impact factor: 3.597