Yoshida M - Search Results

1

Structure-based development of novel substrate-type G9a inhibitors as epigenetic modulators for sickle cell disease treatment.

Nishigaya Y, Takase S, Sumiya T, Sato T, Niwa H, Sato S, Nakata A, Matsuoka S, Maemoto Y, Hashimoto N, Namie R, Honma T, Umehara T, Shirouzu M, Koyama H, Yoshida M, Ito A, Shirai F. Nishigaya Y, et al. Among authors: yoshida m. Bioorg Med Chem Lett. 2024 Sep 15;110:129856. doi: 10.1016/j.bmcl.2024.129856. Epub 2024 Jun 22. Bioorg Med Chem Lett. 2024. PMID: 38914346

2

Design, synthesis, and evaluation of cyclic amide/imide-bearing hydroxamic acid derivatives as class-selective histone deacetylase (HDAC) inhibitors.

Shinji C, Maeda S, Imai K, Yoshida M, Hashimoto Y, Miyachi H. Shinji C, et al. Among authors: yoshida m. Bioorg Med Chem. 2006 Nov 15;14(22):7625-51. doi: 10.1016/j.bmc.2006.07.008. Epub 2006 Jul 31. Bioorg Med Chem. 2006. PMID: 16877001

3

Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors.

Lee S, Shinji C, Ogura K, Shimizu M, Maeda S, Sato M, Yoshida M, Hashimoto Y, Miyachi H. Lee S, et al. Among authors: yoshida m. Bioorg Med Chem Lett. 2007 Sep 1;17(17):4895-900. doi: 10.1016/j.bmcl.2007.06.038. Epub 2007 Jun 13. Bioorg Med Chem Lett. 2007. PMID: 17588744

4

Effects of downregulated HDAC6 expression on the proliferation of lung cancer cells.

Kamemura K, Ito A, Shimazu T, Matsuyama A, Maeda S, Yao TP, Horinouchi S, Khochbin S, Yoshida M. Kamemura K, et al. Among authors: yoshida m. Biochem Biophys Res Commun. 2008 Sep 12;374(1):84-9. doi: 10.1016/j.bbrc.2008.06.092. Epub 2008 Jul 3. Biochem Biophys Res Commun. 2008. PMID: 18602369

5

Isolation of azaspiracid-2 from a marine sponge Echinoclathria sp. as a potent cytotoxin.

Ueoka R, Ito A, Izumikawa M, Maeda S, Takagi M, Shin-ya K, Yoshida M, van Soest RW, Matsunaga S. Ueoka R, et al. Among authors: yoshida m. Toxicon. 2009 May;53(6):680-4. doi: 10.1016/j.toxicon.2009.02.008. Toxicon. 2009. PMID: 19233223

6

Ginkgolic acid inhibits protein SUMOylation by blocking formation of the E1-SUMO intermediate.

Fukuda I, Ito A, Hirai G, Nishimura S, Kawasaki H, Saitoh H, Kimura K, Sodeoka M, Yoshida M. Fukuda I, et al. Among authors: yoshida m. Chem Biol. 2009 Feb 27;16(2):133-40. doi: 10.1016/j.chembiol.2009.01.009. Chem Biol. 2009. PMID: 19246003

7

Kerriamycin B inhibits protein SUMOylation.

Fukuda I, Ito A, Uramoto M, Saitoh H, Kawasaki H, Osada H, Yoshida M. Fukuda I, et al. Among authors: yoshida m. J Antibiot (Tokyo). 2009 Apr;62(4):221-4. doi: 10.1038/ja.2009.10. Epub 2009 Mar 6. J Antibiot (Tokyo). 2009. PMID: 19265871 Free article. No abstract available.

8

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: yoshida m. 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

9

Total synthesis of (+)-chaetocin and its analogues: their histone methyltransferase G9a inhibitory activity.

Iwasa E, Hamashima Y, Fujishiro S, Higuchi E, Ito A, Yoshida M, Sodeoka M. Iwasa E, et al. Among authors: yoshida m. J Am Chem Soc. 2010 Mar 31;132(12):4078-9. doi: 10.1021/ja101280p. J Am Chem Soc. 2010. PMID: 20210309

10

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: yoshida m. 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.

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