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Satoshi Shuto

Showing results (31-40 of 182) with videos related to

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The Journal of Organic Chemistry|April 26, 2003
A systematic study of the hydride reduction of cyclopropyl ketones with structurally simplified substrates. highly stereoselective reductions of trans-substituted cyclopropyl ketones via the bisected s-cis conformationYuji Kazuta, Hiroshi Abe, Tamotsu Yamamoto, et al.
ACS Medicinal Chemistry Letters|March 28, 2015
Identification of 8-aminoadenosine derivatives as a new class of human concentrative nucleoside transporter 2 inhibitorsKazuya Tatani, Masahiro Hiratochi, Yoshinori Nonaka, et al.
The Journal of Organic Chemistry|October 24, 2001
Stereo- and Regioselective Introduction of 1- or 2-Hydroxyethyl Group via Intramolecular Radical Cyclization Reaction with a Novel Silicon-Containing Tether. An Efficient Synthesis of 4'alpha-Branched 2'-Deoxyadenosines(1)Satoshi Shuto, Makiko Kanazaki, Satoshi Ichikawa, et al.
Nucleic Acids Research. Supplement (2001)|August 9, 2003
Synthesis and biological activity of adenophostin derivatives as IP3 receptor ligandsSatoshi Shuto, Tetsuya Mochizuki, Hiroshi Abe, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 15, 2006
Synthesis of cyclic ADP-carbocylcic-xylose and its 3"-O-methyl analogue as stable and potent Ca2+ -mobilizing agentsTakashi Kudoh, Akira Matsuda, Satoshi Shuto, et al.
Organic & Biomolecular Chemistry|August 30, 2013
Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structureShuhei Kawamura, Yuka Unno, Akira Asai, et al.
Molecules (Basel, Switzerland)|August 9, 2020
Conformational Restriction of Histamine with a Rigid Bicyclo[3.1.0]hexane Scaffold Provided Selective H<sub>3</sub> Receptor LigandsMizuki Watanabe, Takaaki Kobayashi, Yoshihiko Ito, et al.
Bioorganic & Medicinal Chemistry|July 12, 2002
Nucleosides and nucleotides. Part 214: thermal stability of triplexes containing 4'alpha-C-aminoalkyl-2'-deoxynucleosidesNaoko Atsumi, Yoshihito Ueno, Makiko Kanazaki, et al.
Journal of Medicinal Chemistry|February 15, 2014
Structurally novel highly potent proteasome inhibitors created by the structure-based hybridization of nonpeptidic belactosin derivatives and peptide boronatesShuhei Kawamura, Yuka Unno, Akira Asai, et al.
International Journal of Pharmaceutics|May 12, 2009
PK-PD modeling of 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine and the enhanced antitumor effect of its phospholipid derivatives in long-circulating liposomesAkitsugu Takada, Hiroyuki Kamiya, Satoshi Shuto, et al.
Pageof 19

Showing results (31-40 of 182) with videos related to

Sort By:
Pageof 19
The Journal of Organic Chemistry|April 26, 2003
A systematic study of the hydride reduction of cyclopropyl ketones with structurally simplified substrates. highly stereoselective reductions of trans-substituted cyclopropyl ketones via the bisected s-cis conformationYuji Kazuta, Hiroshi Abe, Tamotsu Yamamoto, et al.
ACS Medicinal Chemistry Letters|March 28, 2015
Identification of 8-aminoadenosine derivatives as a new class of human concentrative nucleoside transporter 2 inhibitorsKazuya Tatani, Masahiro Hiratochi, Yoshinori Nonaka, et al.
The Journal of Organic Chemistry|October 24, 2001
Stereo- and Regioselective Introduction of 1- or 2-Hydroxyethyl Group via Intramolecular Radical Cyclization Reaction with a Novel Silicon-Containing Tether. An Efficient Synthesis of 4'alpha-Branched 2'-Deoxyadenosines(1)Satoshi Shuto, Makiko Kanazaki, Satoshi Ichikawa, et al.
Nucleic Acids Research. Supplement (2001)|August 9, 2003
Synthesis and biological activity of adenophostin derivatives as IP3 receptor ligandsSatoshi Shuto, Tetsuya Mochizuki, Hiroshi Abe, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 15, 2006
Synthesis of cyclic ADP-carbocylcic-xylose and its 3"-O-methyl analogue as stable and potent Ca2+ -mobilizing agentsTakashi Kudoh, Akira Matsuda, Satoshi Shuto, et al.
Organic & Biomolecular Chemistry|August 30, 2013
Design and synthesis of the stabilized analogs of belactosin A with the unnatural cis-cyclopropane structureShuhei Kawamura, Yuka Unno, Akira Asai, et al.
Molecules (Basel, Switzerland)|August 9, 2020
Conformational Restriction of Histamine with a Rigid Bicyclo[3.1.0]hexane Scaffold Provided Selective H<sub>3</sub> Receptor LigandsMizuki Watanabe, Takaaki Kobayashi, Yoshihiko Ito, et al.
Bioorganic & Medicinal Chemistry|July 12, 2002
Nucleosides and nucleotides. Part 214: thermal stability of triplexes containing 4'alpha-C-aminoalkyl-2'-deoxynucleosidesNaoko Atsumi, Yoshihito Ueno, Makiko Kanazaki, et al.
Journal of Medicinal Chemistry|February 15, 2014
Structurally novel highly potent proteasome inhibitors created by the structure-based hybridization of nonpeptidic belactosin derivatives and peptide boronatesShuhei Kawamura, Yuka Unno, Akira Asai, et al.
International Journal of Pharmaceutics|May 12, 2009
PK-PD modeling of 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine and the enhanced antitumor effect of its phospholipid derivatives in long-circulating liposomesAkitsugu Takada, Hiroyuki Kamiya, Satoshi Shuto, et al.
Pageof 19