Suto Y - Search Results

1

Synthesis and biological evaluation of quinones derived from natural product komaroviquinone as anti-Trypanosoma cruzi agents.

Suto Y, Nakajima-Shimada J, Yamagiwa N, Onizuka Y, Iwasaki G. Suto Y, et al. Bioorg Med Chem Lett. 2015 Aug 1;25(15):2967-71. doi: 10.1016/j.bmcl.2015.05.022. Epub 2015 May 16. Bioorg Med Chem Lett. 2015. PMID: 26037321

2

Synthesis and biological evaluation of the natural product komaroviquinone and related compounds aiming at a potential therapeutic lead compound for high-risk multiple myeloma.

Suto Y, Sato M, Fujimori K, Kitabatake S, Okayama M, Ichikawa D, Matsushita M, Yamagiwa N, Iwasaki G, Kiuchi F, Hattori Y. Suto Y, et al. Bioorg Med Chem Lett. 2017 Oct 1;27(19):4558-4563. doi: 10.1016/j.bmcl.2017.08.054. Epub 2017 Aug 30. Bioorg Med Chem Lett. 2017. PMID: 28882484

3

Synthesis and Evaluation of Quinone Derivatives for Activity against Trypanosome cruzi.

Suto Y, Ascencio T, Nobuta T, Yamagiwa N, Onizuka Y, Ishii M, Kanemitsu K, Nakajima-Shimada J. Suto Y, et al. Chem Pharm Bull (Tokyo). 2021;69(12):1195-1199. doi: 10.1248/cpb.c21-00732. Chem Pharm Bull (Tokyo). 2021. PMID: 34853286 Free article.

4

Convenient method for the addition of disulfides to alkenes.

Yamagiwa N, Suto Y, Torisawa Y. Yamagiwa N, et al. Among authors: suto y. Bioorg Med Chem Lett. 2007 Nov 15;17(22):6197-201. doi: 10.1016/j.bmcl.2007.09.021. Epub 2007 Sep 8. Bioorg Med Chem Lett. 2007. PMID: 17888660

5

A novel derivative (GTN024) from a natural product, komaroviquinone, induced the apoptosis of high-risk myeloma cells via reactive oxygen production and ER stress.

Okayama M, Kitabatake S, Sato M, Fujimori K, Ichikawa D, Matsushita M, Suto Y, Iwasaki G, Yamada T, Kiuchi F, Hirao M, Kunieda H, Osada M, Okamoto S, Hattori Y. Okayama M, et al. Among authors: suto y. Biochem Biophys Res Commun. 2018 Nov 2;505(3):787-793. doi: 10.1016/j.bbrc.2018.09.177. Epub 2018 Oct 5. Biochem Biophys Res Commun. 2018. PMID: 30297108

6

JmjC enzyme KDM2A is a regulator of rRNA transcription in response to starvation.

Tanaka Y, Okamoto K, Teye K, Umata T, Yamagiwa N, Suto Y, Zhang Y, Tsuneoka M. Tanaka Y, et al. Among authors: suto y. EMBO J. 2010 May 5;29(9):1510-22. doi: 10.1038/emboj.2010.56. Epub 2010 Apr 8. EMBO J. 2010. PMID: 20379134 Free PMC article.

7

Cu(I)-catalyzed direct enantioselective cross aldol-type reaction of acetonitrile.

Suto Y, Tsuji R, Kanai M, Shibasaki M. Suto Y, et al. Org Lett. 2005 Aug 18;7(17):3757-60. doi: 10.1021/ol051423e. Org Lett. 2005. PMID: 16092868

8

Dramatic switching of protein kinase C agonist/antagonist activity by modifying the 12-ester side chain of phorbol esters.

Wada R, Suto Y, Kanai M, Shibasaki M. Wada R, et al. Among authors: suto y. J Am Chem Soc. 2002 Sep 11;124(36):10658-9. doi: 10.1021/ja027048s. J Am Chem Soc. 2002. PMID: 12207512

9

Catalytic enantioselective Mannich-type reactions of ketoimines.

Suto Y, Kanai M, Shibasaki M. Suto Y, et al. J Am Chem Soc. 2007 Jan 24;129(3):500-1. doi: 10.1021/ja068226a. J Am Chem Soc. 2007. PMID: 17227007 No abstract available.

10

A new method for the catalytic aldol reaction to ketones.

Oisaki K, Suto Y, Kanai M, Shibasaki M. Oisaki K, et al. Among authors: suto y. J Am Chem Soc. 2003 May 14;125(19):5644-5. doi: 10.1021/ja034993n. J Am Chem Soc. 2003. PMID: 12733898

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