Shuto S - Search Results

1

DJ-1 cooperates with PYCR1 in cell protection against oxidative stress.

Yasuda T, Kaji Y, Agatsuma T, Niki T, Arisawa M, Shuto S, Ariga H, Iguchi-Ariga SM. Yasuda T, et al. Among authors: shuto s. Biochem Biophys Res Commun. 2013 Jun 28;436(2):289-94. doi: 10.1016/j.bbrc.2013.05.095. Epub 2013 Jun 4. Biochem Biophys Res Commun. 2013. PMID: 23743200

2

Synthesis of 5''-substituted cyclic ADP-carbocyclic-ribose as biological tools.

Sakaguchi N, Kudoh T, Murayama T, Arisawa M, Matsuda A, Shuto S. Sakaguchi N, et al. Among authors: shuto s. Nucleic Acids Symp Ser (Oxf). 2006;(50):119-20. doi: 10.1093/nass/nrl059. Nucleic Acids Symp Ser (Oxf). 2006. PMID: 17150846

3

Synthesis of 5''-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety.

Sakaguchi N, Kudoh T, Tsuzuki T, Murayama T, Sakurai T, Matsuda A, Arisawa M, Shuto S. Sakaguchi N, et al. Among authors: shuto s. Bioorg Med Chem Lett. 2008 Jul 1;18(13):3814-8. doi: 10.1016/j.bmcl.2008.04.083. Epub 2008 May 20. Bioorg Med Chem Lett. 2008. PMID: 18534848

4

Synthesis of 2,3- and 3,4-methanoamino acid equivalents with stereochemical diversity and their conversion into the tripeptide proteasome inhibitor belactosin a and its highly potent cis-cyclopropane stereoisomer.

Yoshida K, Yamaguchi K, Sone T, Unno Y, Asai A, Yokosawa H, Matsuda A, Arisawa M, Shuto S. Yoshida K, et al. Among authors: shuto s. Org Lett. 2008 Aug 21;10(16):3571-4. doi: 10.1021/ol8013304. Epub 2008 Jul 19. Org Lett. 2008. PMID: 18642830

5

A method for cleaving an allyl protecting group at the amide nitrogen of peptides by one-pot olefin isomerization-oxidation.

Kajihara K, Arisawa M, Shuto S. Kajihara K, et al. Among authors: shuto s. J Org Chem. 2008 Dec 5;73(23):9494-6. doi: 10.1021/jo801915c. J Org Chem. 2008. PMID: 18980332

6

Three-dimensional structure-activity relationship study of belactosin A and its stereo- and regioisomers: development of potent proteasome inhibitors by a stereochemical diversity-oriented strategy.

Yoshida K, Yamaguchi K, Mizuno A, Unno Y, Asai A, Sone T, Yokosawa H, Matsuda A, Arisawa M, Shuto S. Yoshida K, et al. Among authors: shuto s. Org Biomol Chem. 2009 May 7;7(9):1868-77. doi: 10.1039/b900384c. Epub 2009 Mar 12. Org Biomol Chem. 2009. PMID: 19590782

7

Investigation of the bioactive conformation of histamine H3 receptor antagonists by the cyclopropylic strain-based conformational restriction strategy.

Watanabe M, Hirokawa T, Kobayashi T, Yoshida A, Ito Y, Yamada S, Orimoto N, Yamasaki Y, Arisawa M, Shuto S. Watanabe M, et al. Among authors: shuto s. J Med Chem. 2010 May 13;53(9):3585-93. doi: 10.1021/jm901848b. J Med Chem. 2010. PMID: 20397706

8

Sulfur modification of Au via treatment with Piranha solution provides low-Pd releasing and recyclable Pd material, SAPd.

Hoshiya N, Shimoda M, Yoshikawa H, Yamashita Y, Shuto S, Arisawa M. Hoshiya N, et al. Among authors: shuto s. J Am Chem Soc. 2010 Jun 2;132(21):7270-2. doi: 10.1021/ja9100084. J Am Chem Soc. 2010. PMID: 20462218

9

Alkene isomerization/enamide-ene and diene metathesis for the construction of indoles, quinolines, benzofurans and chromenes with a chiral cyclopropane substituent.

Kobayashi T, Arisawa M, Shuto S. Kobayashi T, et al. Among authors: shuto s. Org Biomol Chem. 2011 Feb 21;9(4):1219-24. doi: 10.1039/c0ob00597e. Epub 2010 Dec 22. Org Biomol Chem. 2011. PMID: 21180704

10

Synthesis of a series of 3,4-methanoarginines as side-chain conformationally restricted analogues of arginine.

Watanabe M, Yamaguchi K, Tang W, Yoshida K, Silverman RB, Arisawa M, Shuto S. Watanabe M, et al. Among authors: shuto s. Bioorg Med Chem. 2011 Oct 15;19(20):5984-8. doi: 10.1016/j.bmc.2011.08.049. Epub 2011 Aug 27. Bioorg Med Chem. 2011. PMID: 21917467

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