Nishino N - Search Results

1

Real-time imaging of histone H4K12-specific acetylation determines the modes of action of histone deacetylase and bromodomain inhibitors.

Ito T, Umehara T, Sasaki K, Nakamura Y, Nishino N, Terada T, Shirouzu M, Padmanabhan B, Yokoyama S, Ito A, Yoshida M. Ito T, et al. Among authors: nishino n. Chem Biol. 2011 Apr 22;18(4):495-507. doi: 10.1016/j.chembiol.2011.02.009. Chem Biol. 2011. PMID: 21513886

2

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.

3

Real-time imaging of histone H4 hyperacetylation in living cells.

Sasaki K, Ito T, Nishino N, Khochbin S, Yoshida M. Sasaki K, et al. Among authors: nishino n. Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16257-62. doi: 10.1073/pnas.0902150106. Epub 2009 Sep 3. Proc Natl Acad Sci U S A. 2009. PMID: 19805290 Free PMC article.

4

Bicyclic tetrapeptide histone deacetylase inhibitors with methoxymethyl ketone and boronic acid zinc-binding groups.

Islam MN, Islam MS, Hoque MA, Kato T, Nishino N, Ito A, Yoshida M. Islam MN, et al. Among authors: nishino n. Bioorg Chem. 2014 Dec;57:121-126. doi: 10.1016/j.bioorg.2014.10.003. Epub 2014 Oct 22. Bioorg Chem. 2014. PMID: 25462987

5

An efficient synthesis of SK-658 and its analogs as potent histone deacetylase inhibitors.

Shahidul Islam M, Nurul Islam M, Ashraful Hoque M, Nishino N, Kato T, Kim HJ, Ito A, Yoshida M. Shahidul Islam M, et al. Among authors: nishino n. Bioorg Chem. 2015 Apr;59:145-50. doi: 10.1016/j.bioorg.2015.02.009. Epub 2015 Mar 7. Bioorg Chem. 2015. PMID: 25797804

6

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

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

Histone deacetylase inhibitors block nuclear factor-κB-dependent transcription by interfering with RNA polymerase II recruitment.

Furumai R, Ito A, Ogawa K, Maeda S, Saito A, Nishino N, Horinouchi S, Yoshida M. Furumai R, et al. Among authors: nishino n. Cancer Sci. 2011 May;102(5):1081-7. doi: 10.1111/j.1349-7006.2011.01904.x. Epub 2011 Mar 4. Cancer Sci. 2011. PMID: 21299717 Free article.

9

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

10

Design and synthesis of peptide-MCA substrates for a novel assay of histone methyltransferases and their inhibitors.

Chi H, Takemoto Y, Nsiama TK, Kato T, Nishino N, Ito A, Yoshida M. Chi H, et al. Among authors: nishino n. Bioorg Med Chem. 2014 Feb 15;22(4):1268-75. doi: 10.1016/j.bmc.2014.01.011. Epub 2014 Jan 21. Bioorg Med Chem. 2014. PMID: 24486204

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