Imaide S - Search Results

1

Synthesis of (-)-homogalanthamine from naltrexone.

Yamamoto N, Fujii H, Imaide S, Hirayama S, Nemoto T, Inokoshi J, Tomoda H, Nagase H. Yamamoto N, et al. Among authors: imaide s. J Org Chem. 2011 Apr 1;76(7):2257-60. doi: 10.1021/jo1022487. Epub 2011 Mar 7. J Org Chem. 2011. PMID: 21381712

2

Investigation of Beckett-Casy model 1: synthesis of novel 16,17-seco-naltrexone derivatives and their pharmacology.

Imaide S, Fujii H, Watanabe A, Nemoto T, Nakajima M, Nakao K, Mochizuki H, Nagase H. Imaide S, et al. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1055-8. doi: 10.1016/j.bmcl.2009.12.039. Epub 2009 Dec 26. Bioorg Med Chem Lett. 2010. PMID: 20056539

3

A double decarboxylation reaction of an oxazolidinone and carboxylic Acid: its application to the synthesis of a new opioid lead compound.

Fujii H, Imaide S, Watanabe A, Yoza K, Nakajima M, Nakao K, Mochizuki H, Sato N, Nemoto T, Nagase H. Fujii H, et al. Among authors: imaide s. J Org Chem. 2010 Feb 5;75(3):995-8. doi: 10.1021/jo9025463. J Org Chem. 2010. PMID: 20070096

4

Investigation of Beckett-Casy model 3: synthesis of novel naltrexone derivatives with contracted and expanded D-rings and their pharmacology.

Nagase H, Imaide S, Tomatsu M, Hirayama S, Nemoto T, Sato N, Nakajima M, Nakao K, Mochizuki H, Gouda H, Hirono S, Fujii H. Nagase H, et al. Among authors: imaide s. Bioorg Med Chem Lett. 2010 Jun 15;20(12):3801-4. doi: 10.1016/j.bmcl.2010.04.044. Epub 2010 Apr 14. Bioorg Med Chem Lett. 2010. PMID: 20478707

5

Investigation of Beckett-Casy model 2: synthesis of novel 15-16 nornaltrexone derivatives and their pharmacology.

Nagase H, Imaide S, Tomatsu M, Nemoto T, Nakajima M, Nakao K, Mochizuki H, Fujii H. Nagase H, et al. Among authors: imaide s. Bioorg Med Chem Lett. 2010 Jun 15;20(12):3726-9. doi: 10.1016/j.bmcl.2010.04.080. Epub 2010 Apr 22. Bioorg Med Chem Lett. 2010. PMID: 20483601

6

Transformation of naltrexone into mesembrane and investigation of the binding properties of its intermediate derivatives to opioid receptors.

Konoura K, Fujii H, Imaide S, Gouda H, Hirayama S, Hirono S, Nagase H. Konoura K, et al. Among authors: imaide s. Bioorg Med Chem. 2015 Feb 1;23(3):439-48. doi: 10.1016/j.bmc.2014.12.032. Epub 2014 Dec 24. Bioorg Med Chem. 2015. PMID: 25573119 Free article.

7

Essential structure of opioid κ receptor agonist nalfurafine for binding to the κ receptor 2: synthesis of decahydro(iminoethano)phenanthrene derivatives and their pharmacologies.

Nagase H, Imaide S, Hirayama S, Nemoto T, Fujii H. Nagase H, et al. Among authors: imaide s. Bioorg Med Chem Lett. 2012 Aug 1;22(15):5071-4. doi: 10.1016/j.bmcl.2012.05.122. Epub 2012 Jun 7. Bioorg Med Chem Lett. 2012. PMID: 22742909

8

Essential structure of opioid κ receptor agonist nalfurafine for binding to κ receptor 1: synthesis of decahydroisoquinoline derivatives and their pharmacologies.

Nagase H, Imaide S, Yamada T, Hirayama S, Nemoto T, Yamaotsu N, Hirono S, Fujii H. Nagase H, et al. Among authors: imaide s. Chem Pharm Bull (Tokyo). 2012;60(8):945-8. doi: 10.1248/cpb.c12-00336. Chem Pharm Bull (Tokyo). 2012. PMID: 22863695 Free article.

9

Essential structure of opioid κ receptor agonist nalfurafine for binding to the κ receptor 3: synthesis of decahydro(iminoethano)phenanthrene derivatives with an oxygen functionality at the 3-position and their pharmacologies.

Fujii H, Imaide S, Hirayama S, Nemoto T, Gouda H, Hirono S, Nagase H. Fujii H, et al. Among authors: imaide s. Bioorg Med Chem Lett. 2012 Dec 15;22(24):7711-4. doi: 10.1016/j.bmcl.2012.09.101. Epub 2012 Oct 5. Bioorg Med Chem Lett. 2012. PMID: 23103094

10

Discovery and SAR Studies of Orally Active Somatostatin Receptor Subtype-2 (SSTR2) Agonists for the Treatment of Acromegaly.

Ishida A, Tajima Y, Okabe Y, Matsushita T, Sekiguchi T, Imaide S, Nomura Y, Tanaka M, Nojima S, Yoshida A, Iyoda Y, Aoki S, Nishio T, Komagata T, Iwaki M, Shono T, Naganawa A, Imagawa A. Ishida A, et al. Among authors: imaide s. ACS Chem Neurosci. 2020 May 20;11(10):1482-1494. doi: 10.1021/acschemneuro.0c00124. Epub 2020 May 1. ACS Chem Neurosci. 2020. PMID: 32315148

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