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Organic Letters|December 25, 2013
Smooth isoindolinone formation from isopropyl carbamates via Bischler-Napieralski-type cyclizationSatoshi Adachi, Masao Onozuka, Yuko Yoshida, et al.
Chemical & Pharmaceutical Bulletin|November 3, 2016
Development of a Method for Converting a TAK1 Type I Inhibitor into a Type II or c-Helix-Out Inhibitor by Structure-Based Drug Design (SBDD)Terushige Muraoka, Mitsuaki Ide, Machiko Irie, et al.
Bioorganic & Medicinal Chemistry Letters|January 23, 2017
Identification of a selective inhibitor of transforming growth factor β-activated kinase 1 by biosensor-based screening of focused librariesTakaaki Miura, Atsushi Matsuo, Terushige Muraoka, et al.
The Journal of Organic Chemistry|August 14, 2010
Synthetic studies on lactonamycins: synthesis of the model BCDEF aglyconKana Watanabe, Yusuke Iwata, Satoshi Adachi, et al.
Bioorganic & Medicinal Chemistry|July 25, 2016
Discovery of a potent and highly selective transforming growth factor β receptor-associated kinase 1 (TAK1) inhibitor by structure based drug design (SBDD)Terushige Muraoka, Mitsuaki Ide, Kenji Morikami, et al.
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