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Journal of Natural Products|January 14, 2022
Chemical Space Expansion of Flavonoids: Induction of Mitotic Inhibition by Replacing Ring B with a 10π-Electron System, Benzo[<i>b</i>]thiopheneSachika Hirazawa, Yohei Saito, Momoko Sagano, et al.
Journal of Natural Products|March 4, 2024
Total Synthesis of a TNBC-Selective Cytotoxic Bromo Nor-eremophilane, PC-A, and Its Preliminary Structure-Activity RelationshipsSayaka Maeda, Wakana Nakayama, Yohei Saito, et al.
ACS Medicinal Chemistry Letters|December 17, 2021
Lead Optimization: Synthesis and Biological Evaluation of PBT-1 Derivatives as Novel Antitumor AgentsLan Xie, Masuo Goto, Xiaoyan Chen, et al.
The Journal of Organic Chemistry|May 25, 2021
Selectfluor-Enabled C(sp<sup>3</sup>)-H Alkoxylation of 3-MethylfuranocoumarinsZengxin Qin, Mengfei Zhao, Kaixin Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|November 6, 2012
1-(3,4,5-Trimethoxyphenyl)ethane-1,2-diyl esters, a novel compound class with potent chemoreversal activityHsin-Yi Hung, Emika Ohkoshi, Masuo Goto, et al.
European Journal of Medicinal Chemistry|September 7, 2018
5'-Chloro-2,2'-dihydroxychalcone and related flavanoids as treatments for prostate cancerYohei Saito, Atsushi Mizokami, Hiroyuki Tsurimoto, et al.
Molecules (Basel, Switzerland)|June 2, 2021
α-Trifluoromethyl Chalcones as Potent Anticancer Agents for Androgen Receptor-Independent Prostate CancerYohei Saito, Atsushi Mizokami, Kouji Izumi, et al.
Journal of Medicinal Chemistry|February 20, 2015
Development of a novel class of tubulin inhibitor from desmosdumotin B with a hydroxylated bicyclic B-ringKyoko Nakagawa-Goto, Akifumi Oda, Ernest Hamel, et al.
Bioorganic & Medicinal Chemistry Letters|June 20, 2017
Design, synthesis and biological evaluation of novel indolin-2-ones as potent anticancer compoundsAndong Zhou, Lei Yan, Fangfang Lai, et al.
ACS Omega|March 1, 2021
Bicyclic Chalcones as Mitotic Inhibitors for Overcoming Androgen Receptor-Independent and Multidrug-Resistant Prostate CancerYohei Saito, Atsushi Mizokami, Sayaka Maeda, et al.
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