Arisawa M - Search Results

1

Conformational restriction approach to β-secretase (BACE1) inhibitors III: effective investigation of the binding mode by combinational use of X-ray analysis, isothermal titration calorimetry and theoretical calculations.

Yonezawa S, Fujiwara K, Yamamoto T, Hattori K, Yamakawa H, Muto C, Hosono M, Tanaka Y, Nakano T, Takemoto H, Arisawa M, Shuto S. Yonezawa S, et al. Among authors: arisawa m. Bioorg Med Chem. 2013 Nov 1;21(21):6506-22. doi: 10.1016/j.bmc.2013.08.036. Epub 2013 Aug 28. Bioorg Med Chem. 2013. PMID: 24051074

2

Anti-inflammatory constituents of topically applied crude drugs. IV. Constituents and anti-inflammatory effect of Paraguayan crude drug "alhucema" (Lavandula latifolia Vill.).

Shimizu M, Shogawa H, Matsuzawa T, Yonezawa S, Hayashi T, Arisawa M, Suzuki S, Yoshizaki M, Morita N, Ferro E, et al. Shimizu M, et al. Among authors: arisawa m. Chem Pharm Bull (Tokyo). 1990 Aug;38(8):2283-4. doi: 10.1248/cpb.38.2283. Chem Pharm Bull (Tokyo). 1990. PMID: 2279292

3

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: arisawa m. Nucleic Acids Symp Ser (Oxf). 2006;(50):119-20. doi: 10.1093/nass/nrl059. Nucleic Acids Symp Ser (Oxf). 2006. PMID: 17150846

4

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: arisawa m. 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

5

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: arisawa m. Org Lett. 2008 Aug 21;10(16):3571-4. doi: 10.1021/ol8013304. Epub 2008 Jul 19. Org Lett. 2008. PMID: 18642830

6

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: arisawa m. J Org Chem. 2008 Dec 5;73(23):9494-6. doi: 10.1021/jo801915c. J Org Chem. 2008. PMID: 18980332

7

Alantrypinone and its derivatives: synthesis and antagonist activity toward insect GABA receptors.

Watanabe T, Arisawa M, Narusuye K, Alam MS, Yamamoto K, Mitomi M, Ozoe Y, Nishida A. Watanabe T, et al. Among authors: arisawa m. Bioorg Med Chem. 2009 Jan 1;17(1):94-110. doi: 10.1016/j.bmc.2008.11.017. Epub 2008 Nov 17. Bioorg Med Chem. 2009. PMID: 19062297

8

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: arisawa m. Org Biomol Chem. 2009 May 7;7(9):1868-77. doi: 10.1039/b900384c. Epub 2009 Mar 12. Org Biomol Chem. 2009. PMID: 19590782

9

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: arisawa m. J Med Chem. 2010 May 13;53(9):3585-93. doi: 10.1021/jm901848b. J Med Chem. 2010. PMID: 20397706

10

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: arisawa m. J Am Chem Soc. 2010 Jun 2;132(21):7270-2. doi: 10.1021/ja9100084. J Am Chem Soc. 2010. PMID: 20462218

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