Nair Reji N, Mishra Jitendra K, Li Fangzheng, Tortosa Mariola, Yang Chunying, Doherty Joanne R, Cameron Michael, Cleveland John L, Roush William R, Bannister Thomas D
Department of Chemistry, The Scripps Research Institute, 110 Scripps Way, Jupiter, FL 33458, USA.
Department of Tumor Biology, Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA.
Medchemcomm. 2016 May 1;7(5):900-905. doi: 10.1039/C5MD00579E. Epub 2016 Feb 23.
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.
设计、合成了单羧酸转运体1型和2型抑制剂(MCT1/2)的谷氨酰胺和酪氨酸基氨基酸缀合物,并评估了它们对表达转运体Asct2、LAT1和MCT1的人B淋巴瘤细胞系增殖的抑制效力。结果表明,氨基酸转运体识别元件的适当定位可增强对Raji细胞的抗肿瘤功效。氨基酸缀合还改善了实验性MCT1/2抑制剂的药效学性质。