Design, Synthesis, and Structure–Activity Relationship of Novel LSD1 Inhibitors Based on Pyrimidine–Thiourea Hybrids As Potent, Orally Active Antitumor Agents
…, M Zhang, JW Wang, L Ding, J Li…
Index: Choi, Yongseok; Li, Ling; Grill, Sue; Gullen, Elizabeth; Lee, Chang Soo; Gumina, Giuseppe; Tsujii, Eisaku; Cheng, Yung-Chi; Chu, Chung K. Journal of Medicinal Chemistry, 2000 , vol. 43, # 13 p. 2538 - 2546
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Citation Number: 20
Abstract
Histone lysine specific demethylase 1 (LSD1) was reported to be overexpressed in several human cancers and recognized as a promising anticancer drug target. In the current study, we designed and synthesized a novel series of pyrimidine–thiourea hybrids and evaluated
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