Iida A - Search Results

1

Multiple structural states of Ca2+-regulated PET hydrolase, Cut190, and its correlation with activity and stability.

Senga A, Numoto N, Yamashita M, Iida A, Ito N, Kawai F, Oda M. Senga A, et al. Among authors: iida a. J Biochem. 2021 Mar 5;169(2):207-213. doi: 10.1093/jb/mvaa102. J Biochem. 2021. PMID: 32882044

2

Synthesis and biological evaluation of histone deacetylase and DNA topoisomerase II-Targeted inhibitors.

Yamashita M, Tahara T, Hayakawa S, Matsumoto H, Wada SI, Tomioka K, Iida A. Yamashita M, et al. Among authors: iida a. Bioorg Med Chem. 2018 May 1;26(8):1920-1928. doi: 10.1016/j.bmc.2018.02.042. Epub 2018 Feb 27. Bioorg Med Chem. 2018. PMID: 29519604

3

STAT3 inhibitory activity of naphthoquinones isolated from Tabebuia avellanedae.

Tahara T, Watanabe A, Yutani M, Yamano Y, Sagara M, Nagai S, Saito K, Yamashita M, Ihara M, Iida A. Tahara T, et al. Among authors: iida a. Bioorg Med Chem. 2020 Mar 15;28(6):115347. doi: 10.1016/j.bmc.2020.115347. Epub 2020 Jan 28. Bioorg Med Chem. 2020. PMID: 32044231

4

Concise synthesis of heterocycle-fused naphthoquinones by employing sonogashira coupling and tandem addition-elimination/intramolecular cyclization.

Ueda K, Yamashita M, Sakaguchi K, Tokuda H, Iida A. Ueda K, et al. Among authors: iida a. Chem Pharm Bull (Tokyo). 2013;61(6):648-54. doi: 10.1248/cpb.c13-00102. Chem Pharm Bull (Tokyo). 2013. PMID: 23727778 Free article.

5

Design, synthesis, and evaluation of DNA topoisomerase II-targeted nucleosides.

Matsumoto H, Yamashita M, Tahara T, Hayakawa S, Wada SI, Tomioka K, Iida A. Matsumoto H, et al. Among authors: iida a. Bioorg Med Chem. 2017 Aug 1;25(15):4133-4144. doi: 10.1016/j.bmc.2017.06.001. Epub 2017 Jun 2. Bioorg Med Chem. 2017. PMID: 28619446

6

Structure-Activity Relationship Studies of Antimicrobial Naphthoquinones Derived from Constituents of Tabebuia avellanedae.

Yamashita M, Sawano J, Umeda R, Tatsumi A, Kumeda Y, Iida A. Yamashita M, et al. Among authors: iida a. Chem Pharm Bull (Tokyo). 2021;69(7):661-673. doi: 10.1248/cpb.c21-00208. Chem Pharm Bull (Tokyo). 2021. PMID: 34193715 Free article.

7

One-pot synthesis of benzo[f]indole-4,9-diones from 1,4-naphthoquinones and terminal acetylenes.

Yamashita M, Ueda K, Sakaguchi K, Tokuda H, Iida A. Yamashita M, et al. Among authors: iida a. Chem Pharm Bull (Tokyo). 2011;59(10):1289-93. doi: 10.1248/cpb.59.1289. Chem Pharm Bull (Tokyo). 2011. PMID: 21963641 Free article.

8

The anti-obesity effect of Taheebo (Tabebuia avellanedae Lorentz ex Griseb) extract in ovariectomized mice and the identification of a potential anti-obesity compound.

Iwamoto K, Fukuda Y, Tokikura C, Noda M, Yamamoto A, Yamamoto M, Yamashita M, Zaima N, Iida A, Moriyama T. Iwamoto K, et al. Among authors: iida a. Biochem Biophys Res Commun. 2016 Sep 23;478(3):1136-40. doi: 10.1016/j.bbrc.2016.08.081. Epub 2016 Aug 15. Biochem Biophys Res Commun. 2016. PMID: 27539320

9

Stereoselective synthesis and cytotoxicity of a cancer chemopreventive naphthoquinone from Tabebuia avellanedae.

Yamashita M, Kaneko M, Iida A, Tokuda H, Nishimura K. Yamashita M, et al. Among authors: iida a. Bioorg Med Chem Lett. 2007 Dec 1;17(23):6417-20. doi: 10.1016/j.bmcl.2007.10.005. Epub 2007 Oct 5. Bioorg Med Chem Lett. 2007. PMID: 17950604

10

Synthesis and evaluation of bioactive naphthoquinones from the Brazilian medicinal plant, Tabebuia avellanedae.

Yamashita M, Kaneko M, Tokuda H, Nishimura K, Kumeda Y, Iida A. Yamashita M, et al. Among authors: iida a. Bioorg Med Chem. 2009 Sep 1;17(17):6286-91. doi: 10.1016/j.bmc.2009.07.039. Epub 2009 Jul 23. Bioorg Med Chem. 2009. PMID: 19674905

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