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Preclinical studies of the triazolo[1,5-a]pyrimidine derivative WS-716 as a highly potent, specific and orally active P-glycoprotein (P-gp) inhibitor.
Wang SQ, Teng QX, Wang S, Lei ZN, Hu HH, Lv HF, Chen BB, Wang JZ, Shi XJ, Xu WF, Liu HM, Chen XB, Chen ZS, Yu B. Wang SQ, et al. Among authors: wang jz, wang s. Acta Pharm Sin B. 2022 Aug;12(8):3263-3280. doi: 10.1016/j.apsb.2022.03.023. Epub 2022 Apr 2. Acta Pharm Sin B. 2022. PMID: 35967279 Free PMC article.
Design, synthesis, and structure-activity relationship of novel LSD1 inhibitors based on pyrimidine-thiourea hybrids as potent, orally active antitumor agents.
Ma LY, Zheng YC, Wang SQ, Wang B, Wang ZR, Pang LP, Zhang M, Wang JW, Ding L, Li J, Wang C, Hu B, Liu Y, Zhang XD, Wang JJ, Wang ZJ, Zhao W, Liu HM. Ma LY, et al. Among authors: wang sq, wang jw, wang jj, wang zj, wang zr, wang c, wang b. J Med Chem. 2015 Feb 26;58(4):1705-16. doi: 10.1021/acs.jmedchem.5b00037. Epub 2015 Feb 6. J Med Chem. 2015. PMID: 25610955
1,370 results