C–H activation enables a rapid structure–activity relationship study of arylcyclopropyl amines for potent and selective LSD1 inhibitors. Issue 36 (22nd August 2016)

• Record Type: Journal Article
• Authors: Miyamura, Shin; Araki, Misaho; Ota, Yosuke; Itoh, Yukihiro; Yasuda, Shusuke; Masuda, Mitsuharu; Taniguchi, Tomoyuki; Sowa, Yoshihiro; Sakai, Toshiyuki; Suzuki, Takayoshi; Itami, Kenichiro; Yamaguchi, Junichiro
• Is Part Of: Organic & biomolecular chemistry. Volume 14:Issue 36(2016)
• Page Start: 8576
• Page End: 8585
• Publication Date: 2016-08-22
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c6ob01483f
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : Potent and selective LSD1 inhibitors were synthesized rapidly by a C–H borylation and cross-coupling sequence. Abstract : We describe the structure–activity relationship of various arylcyclopropylamines (ACPAs), which are potent LSD1 inhibitors. More than 45 ACPAs were synthesized rapidly by an unconventional method that we have recently developed, consisting of a C–H borylation and cross-coupling sequence starting from cyclopropylamine. We also generated NCD38 derivatives, which are known as LSD1 selective inhibitors, and discovered a more effective inhibitor compared to the original NCD38.