Yasuda D - Search Results

1

Ropinirole, a New ALS Drug Candidate Developed Using iPSCs.

Okano H, Yasuda D, Fujimori K, Morimoto S, Takahashi S. Okano H, et al. Among authors: yasuda d. Trends Pharmacol Sci. 2020 Feb;41(2):99-109. doi: 10.1016/j.tips.2019.12.002. Epub 2020 Jan 8. Trends Pharmacol Sci. 2020. PMID: 31926602 Free article. Review.

2

[Young Innovators Driving the Next Generation of Academic Drug Discovery].

Matsumaru T, Yasuda D. Matsumaru T, et al. Among authors: yasuda d. Yakugaku Zasshi. 2018;138(8):1025-1026. doi: 10.1248/yakushi.17-00211-F. Yakugaku Zasshi. 2018. PMID: 30068842 Free article. Japanese. No abstract available.

3

Antioxidant activities of 5-hydroxyoxindole and its 3-hydroxy-3-phenacyl derivatives: the suppression of lipid peroxidation and intracellular oxidative stress.

Yasuda D, Takahashi K, Ohe T, Nakamura S, Mashino T. Yasuda D, et al. Bioorg Med Chem. 2013 Dec 15;21(24):7709-14. doi: 10.1016/j.bmc.2013.10.021. Epub 2013 Oct 30. Bioorg Med Chem. 2013. PMID: 24216095

4

Synthesis of novel benzbromarone derivatives designed to avoid metabolic activation.

Ohe T, Umezawa R, Kitagawara Y, Yasuda D, Takahashi K, Nakamura S, Abe A, Sekine S, Ito K, Okunushi K, Morio H, Furihata T, Anzai N, Mashino T. Ohe T, et al. Among authors: yasuda d. Bioorg Med Chem Lett. 2018 Dec 15;28(23-24):3708-3711. doi: 10.1016/j.bmcl.2018.10.023. Epub 2018 Oct 15. Bioorg Med Chem Lett. 2018. PMID: 30389287

5

Synthesis and evaluation of nevirapine analogs to study the metabolic activation of nevirapine.

Tateishi Y, Ohe T, Yasuda D, Takahashi K, Nakamura S, Kazuki Y, Mashino T. Tateishi Y, et al. Among authors: yasuda d. Drug Metab Pharmacokinet. 2020 Apr;35(2):238-243. doi: 10.1016/j.dmpk.2020.01.006. Epub 2020 Feb 28. Drug Metab Pharmacokinet. 2020. PMID: 32184040

6

A 5-hydroxyoxindole derivative attenuates LPS-induced inflammatory responses by activating the p38-Nrf2 signaling axis.

Niino T, Tago K, Yasuda D, Takahashi K, Mashino T, Tamura H, Funakoshi-Tago M. Niino T, et al. Among authors: yasuda d. Biochem Pharmacol. 2018 Sep;155:182-197. doi: 10.1016/j.bcp.2018.06.021. Epub 2018 Jun 22. Biochem Pharmacol. 2018. PMID: 29940171

7

[Hit-to-Lead in Academia: Discovery of a Protein-Protein Interaction Inhibitor of Keap1-Nrf2].

Yasuda D, Obata R, Takahashi K, Ohe T, Mashino T. Yasuda D, et al. Yakugaku Zasshi. 2018;138(8):1059-1065. doi: 10.1248/yakushi.17-00211-5. Yakugaku Zasshi. 2018. PMID: 30068847 Free article. Review. Japanese.

8

Inhibitors of the protein-protein interaction between phosphorylated p62 and Keap1 attenuate chemoresistance in a human hepatocellular carcinoma cell line.

Yasuda D, Ohe T, Takahashi K, Imamura R, Kojima H, Okabe T, Ichimura Y, Komatsu M, Yamamoto M, Nagano T, Mashino T. Yasuda D, et al. Free Radic Res. 2020 Dec;54(11-12):859-871. doi: 10.1080/10715762.2020.1732955. Epub 2020 Mar 30. Free Radic Res. 2020. PMID: 32075457

9

Effects of Ramelteon and Other Sleep-Promoting Drugs on Serum Low-Density Lipoprotein and Non-high-density Lipoprotein Cholesterol: A Retrospective Comparative Pilot Study.

Torii H, Shimizu R, Tanizaki Y, Omiya Y, Yamamoto M, Kamiike S, Yasuda D, Hiraoka Y, Hashida T, Kume N. Torii H, et al. Among authors: yasuda d. Biol Pharm Bull. 2018;41(12):1778-1790. doi: 10.1248/bpb.b18-00411. Biol Pharm Bull. 2018. PMID: 30504680 Free article.

10

Synthesis of Keap1-phosphorylated p62 and Keap1-Nrf2 protein-protein interaction inhibitors and their inhibitory activity.

Yasuda D, Nakajima M, Yuasa A, Obata R, Takahashi K, Ohe T, Ichimura Y, Komatsu M, Yamamoto M, Imamura R, Kojima H, Okabe T, Nagano T, Mashino T. Yasuda D, et al. Bioorg Med Chem Lett. 2016 Dec 15;26(24):5956-5959. doi: 10.1016/j.bmcl.2016.10.083. Epub 2016 Oct 27. Bioorg Med Chem Lett. 2016. PMID: 27839920

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