北海道大学大学院 薬学研究院 創薬科学部門 創薬化学分野
薬化学研究室 Laboratory of Medicinal Chemistry
 

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 発表論文 2011

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  1. 1.松田 彰
    ヌクレアーゼ抵抗性化学修飾核酸の開発研究
    薬学雑誌, 2011, 131, 285-298. DOI:10.1248/yakushi.131.285

  2. 2.谷野 哲也、市川 聡、魚谷 幸一、大山 洋、松田 彰
    新規抗菌剤開発を指向したMraY阻害天然物ムライマイシン類の合成研究
    薬学雑誌、2011, 131, 335-346. DOI:10.1248/yakushi.131.335

  3. 3.Hirama, Y.; Minakawa, N.; Matsuda, A.
    Synthesis and characterization of oligodeoxynucleotides containing a novel tetraazabenzo[cd]azulene:naphthyridine base pair.
    Bioorg. Med. Chem. 2011, 19, 352-358. DOI:10.1016/j.bmc.2010.11.023
           


  4. 4.Fruita, K.; Murata, S.; Jee, J. G.; Ichikawa, S.; Matsuda, A.; Kojima, C.
    Structural feature of bent DNA recognized by HMGB1.
    J. Am. Chem. Soc. 2011, 133, 5788-5790. DOI: 10.1021/ja2013399

  5. 5.Kataoka, M.; Kouda, Y.; Sato, K.; Minakawa, N.; Matsuda, A.
    Highly efficient enzymatic synthesis of 3´-deoxyapionucleic acid (apioNA) having the four natural nucleobases.
    Chem. Commun. 2011, 47, 8700-8702. DOI: 10.1039/C1CC12980E



  6. 6.Tanino, T.; Ichikawa, S.; Matsuda, A.
    Synthesis of L-epi-Capreomycidine Derivatives via C–H Amination.
    Org. Lett. 2011, 13, 4028-4031. DOI: 10.1021/ol201527k


  7. 7.Ichikawa, S.; Tanino, T.; Ii, K.; Matsuda, A.
    Development of antibacterial agents against drug-resistant bacterial pathogens based on total synthesis of nucleoside natural products.
    有機合成化学協会誌, 2011, 69, 1020-1033.

  8. 8.Kuramoto, K.; Tarashima, N.; Hirama, Y.; Kikuchi, Y.; Minakawa, N.; Matsuda, A.
    New imidazopyridopyrimidine:naphthyridine base-pairing motif, ImNN:NaOO, consisting of a DAAD:ADDA hydrogen bonding pattern, markedly stabilize DNA duplexes.
    Chem. Commun. 2011, 47, 10818-10820. DOI: 10.1039/c1cc13805g


  9. 9.Taniike, H.; Inagaki, Y.; Matsuda, A.; Minakawa, N.
    Practical synthesis of 4´-selenopyrimidine nucleosides using hypervalent iodine.
    Tetrahedron 2011, 67, 7977-7982. DOI: 10.1016/j.tet.2011.08.020

  10. 10.Okamoto, K.; Sakagami, M.; Feng, F.; Togame, H.; Takemoto, H.; Ichikawa, S.; Matsuda, A.
    Total Synthesis of Pacidamycin D by Cu(I)-Catalyzed Oxy Enamide Formation.
    Org. Lett. 2011, 13, 5240-5243. DOI: 10.1021/ol202124b


  11. 11.Meike, S.; Yamamori, T.; Yasui, H.; Eitaki, M.; Matsuda, A.; Inanami, O.
    8-Aminoadenosine Enhances Radiation-induced Cell Death in Human Lung Carcinoma A549 Cells.
    J. Rad. Res. 2011, 52, 456-463. DOI: 10.1269/jrr.10188

  12. 12.Meike, S.; Yamamori, T.; Yasui, H.; Eitaki, M.; Matsuda, A.; Inanami, O.
    A nucleoside anticancer drug, 1-(3-C-ethynyl-β-D-ribo-pentofuranosyl)cytosine (TAS106), sensitizes cells to radiation by suppressing BRCA2 expression.
    Mol. Cancer 2011, 10, 92-100. DOI: 10.1186/1476-4598-10-92

  13. 13.Hori, M.; Suzuki, T.; Minakawa, N.; Matsuda, A.; Harashima, H.; Kamiya, H.
    Mutagenicity of secondary oxidation products of 8-oxo-7,8-dihydro-2´-deoxyguanosine 5´-triphosphate (8-hydroxy-2´-deoxyguanosine 5´-triphosphate).
    Mutation Res., Fundamental and Molecular Mechanisms of Mutagenesis 2011, 714, 11-16.
    DOI:
    10.1016/j.mrfmmm.2011.05.015

  14. 14.Hirose, W.; Sato, K.; Matsuda, A.
    Fluorescence Properties of 5-(5,6-Dimethoxybenzothiazol-2-yl)-2´-Deoxyuridine (dbtU) and Oligodeoxyribonucleotides containing dbtU.
    Eur. J. Org. Chem. 2011, 2011, 6206-6217. DOI: 10.1002/ejoc.201100818


  15. 15.Sato, K.; Sasaki, A.; Matsuda, A.
    Highly Fluorescent 5-(5,6-Dimethoxybenzothiazol-2-yl)-2´-Deoxyuridine 5´-Triphosphate as an Efficient Substrate for DNA Polymerases.
    ChemBioChem 2011, 12, 2341-2346. DOI: 10.1002/cbic.201100452

    Cover Picture of ChemBioChem 2011, 12, issue 15. DOI: 10.1002/cbic.201190069



  1. 16.Muranaka, K.; Ichikawa, S.; Matsuda, A.
    Development of the Carboxamine Protection Group, 4-(tert-Butyldimethylsiloxy)-2-methoxybenzyl.
    J. Org. Chem. 2011, 76, 9278-9293. DOI: 10.1021/jo201495w



  1. 17.Tanino, T.; Al-Dabbagh, B.; Mengin-Lecreulx, D.; Bouhss, A.; Oyama, H.; Ichikawa, S.; Matsuda, A.
    Mechanistic Analysis of Muraymycin Analogues: A Guide to the Design of MraY Inhibitors.
    J. Med. Chem. 2011, 54, 8421-8439. DOI: 10.1021/jm200906r