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BibliographyContents
Synthesis and application of an N(δ)-acetyl-N(δ)-hydroxyornithine analog: Identification of novel metal complexes of deferriferrichrysin
  Kobayashi, Kazuya, Oishi, Shinya, Kobayashi, Yuka, Ohno, Hiroaki, Tsutsumi, Hiroko, Hata, Yoji, Fujii, Nobutaka (2012-04-15)
  Bioorganic & medicinal chemistry, 20(8): 2651-2655
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Electrostatically constrained α-helical peptide inhibits replication of HIV-1 resistant to enfuvirtide
  Nishikawa, Hiroki, Nakamura, Shota, Kodama, Eiichi, Ito, Saori, Kajiwara, Keiko, Izumi, Kazuki, Sakagami, Yasuko, Oishi, Shinya, Ohkubo, Tadayasu, Kobayashi, Yuji, Otaka, Akira, Fujii, Nobutaka, Matsuoka, Masao (2009-04)
  The international journal of biochemistry & cell biology, 41(4): 891-899
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Novel screening systems for HIV-1 fusion mediated by two extra-virion heptad repeats of gp41
  Nishikawa, Hiroki, Kodama, Eiichi, Sakakibara, Ayako, Fukudome, Ayako, Izumi, Kazuki, Oishi, Shinya, Fujii, Nobutaka, Matsuoka, Masao (2008-10)
  Antiviral research, 80(1): 71-76
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Efficient synthesis of aminomethylated azaindoles and corresponding pyrrole-fused derivatives by copper-catalyzed domino multicomponent coupling and cyclization
  Hou, Zengye, Suzuki, Yamato, Oishi, Shinya, Fujii, Nobutaka, Ohno, Hiroaki (2012-02)
  Tetrahedron, 68(6): 1695-1703
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Pachastrissamine (jaspine B) and its stereoisomers inhibit sphingosine kinases and atypical protein kinase C
  Yoshimitsu, Yuji, Oishi, Shinya, Miyagaki, Jun, Inuki, Shinsuke, Ohno, Hiroaki, Fujii, Nobutaka (2011-09-15)
  Bioorganic & medicinal chemistry, 19(18): 5402-5408
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Structure–activity relationship study on senktide for development of novel potent neurokinin-3 receptor selective agonists
  Misu, Ryosuke, Yamamoto, Koki, Yamada, Ai, Noguchi, Taro, Ohno, Hiroaki, Yamamura, Takashi, Okamura, Hiroaki, Matsuda, Fuko, Ohkura, Satoshi, Oishi, Shinya, Fujii, Nobutaka (2015-01-05)
  MedChemComm, 6(3): 469-476
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Formal [4+2] reaction between 1,3-diynes and pyrroles: gold(I)-catalyzed indole synthesis by double hydroarylation
  Matsuda, Yuka, Naoe, Saori, Oishi, Shinya, Fujii, Nobutaka, Ohno, Hiroaki (2014-11-28)
  Chemistry : A European Journal, 21(4): 1463-1467
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Optimization of diaryl amine derivatives as kinesin spindle protein inhibitors
  Takeuchi, Tomoki, Oishi, Shinya, Kaneda, Masato, Misu, Ryosuke, Ohno, Hiroaki, Sawada, Jun-ichi, Asai, Akira, Nakamura, Shinya, Nakanishi, Isao, Fujii, Nobutaka (2014-06-15)
  Bioorganic & medicinal chemistry, 22(12): 3171-3179
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Design and synthesis of fluorescent probes for GPR54
  Kaneda, Masato, Misu, Ryosuke, Ohno, Hiroaki, Hirasawa, Akira, Ieda, Nahoko, Uenoyama, Yoshihisa, Tsukamura, Hiroko, Maeda, Kei-ichiro, Oishi, Shinya, Fujii, Nobutaka (2014-07-01)
  Bioorganic & medicinal chemistry, 22(13): 3325-3330
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Diversity-oriented synthesis of pyrazolo[4,3-b]indoles by gold-catalysed three-component annulation: application to the development of a new class of CK2 inhibitors
  Hou, Zengye, Oishi, Shinya, Suzuki, Yamato, Kure, Tatsuhide, Nakanishi, Isao, Hirasawa, Akira, Tsujimoto, Gozoh, Ohno, Hiroaki, Fujii, Nobutaka (2013-05-28)
  Organic & biomolecular chemistry, 11(20): 3288-3296
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