Sato S - Search Results

1

Development and Structural Evaluation of N-Alkylated trans-2-Phenylcyclopropylamine-Based LSD1 Inhibitors.

Niwa H, Sato S, Handa N, Sengoku T, Umehara T, Yokoyama S. Niwa H, et al. Among authors: sato s. ChemMedChem. 2020 May 6;15(9):787-793. doi: 10.1002/cmdc.202000014. Epub 2020 Mar 30. ChemMedChem. 2020. PMID: 32166890

2

Solution structure of histone chaperone ANP32B: interaction with core histones H3-H4 through its acidic concave domain.

Tochio N, Umehara T, Munemasa Y, Suzuki T, Sato S, Tsuda K, Koshiba S, Kigawa T, Nagai R, Yokoyama S. Tochio N, et al. Among authors: sato s. J Mol Biol. 2010 Aug 6;401(1):97-114. doi: 10.1016/j.jmb.2010.06.005. Epub 2010 Jun 9. J Mol Biol. 2010. PMID: 20538007

3

Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1.

Mimasu S, Umezawa N, Sato S, Higuchi T, Umehara T, Yokoyama S. Mimasu S, et al. Among authors: sato s. Biochemistry. 2010 Aug 3;49(30):6494-503. doi: 10.1021/bi100299r. Biochemistry. 2010. PMID: 20568732

4

Crystallographic study of a site-specifically cross-linked protein complex with a genetically incorporated photoreactive amino acid.

Sato S, Mimasu S, Sato A, Hino N, Sakamoto K, Umehara T, Yokoyama S. Sato S, et al. Among authors: sato a. Biochemistry. 2011 Jan 18;50(2):250-7. doi: 10.1021/bi1016183. Epub 2010 Dec 16. Biochemistry. 2011. PMID: 21128684

5

Multiple site-specific installations of Nε-monomethyl-L-lysine into histone proteins by cell-based and cell-free protein synthesis.

Yanagisawa T, Takahashi M, Mukai T, Sato S, Wakamori M, Shirouzu M, Sakamoto K, Umehara T, Yokoyama S. Yanagisawa T, et al. Among authors: sato s. Chembiochem. 2014 Aug 18;15(12):1830-8. doi: 10.1002/cbic.201402291. Epub 2014 Jul 25. Chembiochem. 2014. PMID: 25067793

6

Development of a hexahistidine-3× FLAG-tandem affinity purification method for endogenous protein complexes in Pichia pastoris.

Higo T, Suka N, Ehara H, Wakamori M, Sato S, Maeda H, Sekine S, Umehara T, Yokoyama S. Higo T, et al. Among authors: sato s. J Struct Funct Genomics. 2014 Dec;15(4):191-9. doi: 10.1007/s10969-014-9190-1. Epub 2014 Nov 15. J Struct Funct Genomics. 2014. PMID: 25398586 Free PMC article.

7

Activation of lysine-specific demethylase 1 inhibitor peptide by redox-controlled cleavage of a traceless linker.

Amano Y, Umezawa N, Sato S, Watanabe H, Umehara T, Higuchi T. Amano Y, et al. Among authors: sato s. Bioorg Med Chem. 2017 Feb 1;25(3):1227-1234. doi: 10.1016/j.bmc.2016.12.033. Epub 2016 Dec 23. Bioorg Med Chem. 2017. PMID: 28065500

8

Development and crystallographic evaluation of histone H3 peptide with N-terminal serine substitution as a potent inhibitor of lysine-specific demethylase 1.

Amano Y, Kikuchi M, Sato S, Yokoyama S, Umehara T, Umezawa N, Higuchi T. Amano Y, et al. Among authors: sato s. Bioorg Med Chem. 2017 May 1;25(9):2617-2624. doi: 10.1016/j.bmc.2017.03.016. Epub 2017 Mar 9. Bioorg Med Chem. 2017. PMID: 28336409

9

Lysine-specific demethylase 1 inhibitors prevent teratoma development from human induced pluripotent stem cells.

Osada N, Kikuchi J, Umehara T, Sato S, Urabe M, Abe T, Hayashi N, Sugitani M, Hanazono Y, Furukawa Y. Osada N, et al. Among authors: sato s. Oncotarget. 2018 Jan 8;9(5):6450-6462. doi: 10.18632/oncotarget.24030. eCollection 2018 Jan 19. Oncotarget. 2018. PMID: 29464084 Free PMC article.

10

Development of Novel Inhibitors for Histone Methyltransferase SET7/9 based on Cyproheptadine.

Hirano T, Fujiwara T, Niwa H, Hirano M, Ohira K, Okazaki Y, Sato S, Umehara T, Maemoto Y, Ito A, Yoshida M, Kagechika H. Hirano T, et al. Among authors: sato s. ChemMedChem. 2018 Aug 10;13(15):1530-1540. doi: 10.1002/cmdc.201800233. Epub 2018 Jul 6. ChemMedChem. 2018. PMID: 29882380

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