Nishino N - Search Results

1

Cyclic tetrapeptides bearing a sulfhydryl group potently inhibit histone deacetylases.

Nishino N, Jose B, Okamura S, Ebisusaki S, Kato T, Sumida Y, Yoshida M. Nishino N, et al. Org Lett. 2003 Dec 25;5(26):5079-82. doi: 10.1021/ol036098e. Org Lett. 2003. PMID: 14682769

2

Synthesis and histone deacetylase inhibitory activity of cyclic tetrapeptides containing a retrohydroxamate as zinc ligand.

Nishino N, Yoshikawa D, Watanabe LA, Kato T, Jose B, Komatsu Y, Sumida Y, Yoshida M. Nishino N, et al. Bioorg Med Chem Lett. 2004 May 17;14(10):2427-31. doi: 10.1016/j.bmcl.2004.03.018. Bioorg Med Chem Lett. 2004. PMID: 15109626

3

Novel histone deacetylase inhibitors: cyclic tetrapeptide with trifluoromethyl and pentafluoroethyl ketones.

Jose B, Oniki Y, Kato T, Nishino N, Sumida Y, Yoshida M. Jose B, et al. Among authors: nishino n. Bioorg Med Chem Lett. 2004 Nov 1;14(21):5343-6. doi: 10.1016/j.bmcl.2004.08.016. Bioorg Med Chem Lett. 2004. PMID: 15454224

4

Chlamydocin-hydroxamic acid analogues as histone deacetylase inhibitors.

Nishino N, Jose B, Shinta R, Kato T, Komatsu Y, Yoshida M. Nishino N, et al. Bioorg Med Chem. 2004 Nov 15;12(22):5777-84. doi: 10.1016/j.bmc.2004.08.041. Bioorg Med Chem. 2004. PMID: 15498654

5

Chlamydocin analogs bearing carbonyl group as possible ligand toward zinc atom in histone deacetylases.

Bhuiyan MP, Kato T, Okauchi T, Nishino N, Maeda S, Nishino TG, Yoshida M. Bhuiyan MP, et al. Among authors: nishino tg, nishino n. Bioorg Med Chem. 2006 May 15;14(10):3438-46. doi: 10.1016/j.bmc.2005.12.063. Epub 2006 Jan 24. Bioorg Med Chem. 2006. PMID: 16439135

6

Interaction of aliphatic cap group in inhibition of histone deacetylases by cyclic tetrapeptides.

Nishino N, Shivashimpi GM, Soni PB, Bhuiyan MP, Kato T, Maeda S, Nishino TG, Yoshida M. Nishino N, et al. Among authors: nishino tg. Bioorg Med Chem. 2008 Jan 1;16(1):437-45. doi: 10.1016/j.bmc.2007.09.021. Epub 2007 Sep 15. Bioorg Med Chem. 2008. PMID: 17900911

7

Bicyclic peptides as potent inhibitors of histone deacetylases: optimization of alkyl loop length.

Islam NM, Kato T, Nishino N, Kim HJ, Ito A, Yoshida M. Islam NM, et al. Among authors: nishino n. Bioorg Med Chem Lett. 2010 Feb 1;20(3):997-9. doi: 10.1016/j.bmcl.2009.12.054. Epub 2009 Dec 21. Bioorg Med Chem Lett. 2010. PMID: 20045316

8

Cyclic tetrapeptides with thioacetate tails or intramolecular disulfide bridge as potent inhibitors of histone deacetylases.

Hoque MA, Arai T, Nishino N, Kim HJ, Ito A, Yoshida M. Hoque MA, et al. Among authors: nishino n. Bioorg Med Chem Lett. 2012 Nov 1;22(21):6770-2. doi: 10.1016/j.bmcl.2012.03.004. Epub 2012 Mar 8. Bioorg Med Chem Lett. 2012. PMID: 23021104

9

From discovery to the coming generation of histone deacetylase inhibitors.

Yoshida M, Matsuyama A, Komatsu Y, Nishino N. Yoshida M, et al. Among authors: nishino n. Curr Med Chem. 2003 Nov;10(22):2351-8. doi: 10.2174/0929867033456602. Curr Med Chem. 2003. PMID: 14529478 Review.

10

Toward an HDAC6 inhibitor: synthesis and conformational analysis of cyclic hexapeptide hydroxamic acid designed from alpha-tubulin sequence.

Jose B, Okamura S, Kato T, Nishino N, Sumida Y, Yoshida M. Jose B, et al. Among authors: nishino n. Bioorg Med Chem. 2004 Mar 15;12(6):1351-6. doi: 10.1016/j.bmc.2004.01.014. Bioorg Med Chem. 2004. PMID: 15018907

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