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Akira Otaka

Showing results (101-110 of 123) with videos related to

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The Journal of Endocrinology|January 14, 2025
Effects of tryptophan-selective lipidated glucagon-like peptide 1 (GLP-1) peptides on the GLP-1 receptorXuejing Lu, Norio Harada, Takuma Yasuda, et al.
Bioorganic & Medicinal Chemistry Letters|October 26, 2005
Design and synthesis of downsized metastin (45-54) analogs with maintenance of high GPR54 agonistic activityAyumu Niida, Zixuan Wang, Kenji Tomita, et al.
The Journal of Biological Chemistry|February 18, 2006
Specific recognition of the collagen triple helix by chaperone HSP47. II. The HSP47-binding structural motif in collagens and related proteinsTakaki Koide, Yoshimi Nishikawa, Shinichi Asada, et al.
Journal of Medicinal Chemistry|April 18, 2003
Reduction of peptide character of HIV protease inhibitors that exhibit nanomolar potency against multidrug resistant HIV-1 strainsHirokazu Tamamura, Yasuhiro Koh, Satoshi Ueda, et al.
Organic & Biomolecular Chemistry|May 9, 2014
Development of a traceable linker containing a thiol-responsive amino acid for the enrichment and selective labelling of target proteinsJun Yamamoto, Masaya Denda, Nami Maeda, et al.
Angewandte Chemie (International Ed. in English)|February 25, 2021
Discovery of a Macropinocytosis-Inducing Peptide Potentiated by Medium-Mediated Intramolecular Disulfide FormationJan Vincent V Arafiles, Hisaaki Hirose, Yusuke Hirai, et al.
The Journal of Organic Chemistry|May 6, 2006
Stereoselective synthesis of 3,6-disubstituted-3,6-dihydropyridin-2-ones as potential diketopiperazine mimetics using organocopper-mediated anti-SN2' reactions and their use in the preparation of low-molecule CXCR4 antagonistsAyumu Niida, Hiroaki Tanigaki, Eriko Inokuchi, et al.
Organic & Biomolecular Chemistry|December 3, 2003
Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivativesHirokazu Tamamura, Kenichi Hiramatsu, a Shuichi Kusano, et al.
Journal of Medicinal Chemistry|January 22, 2005
Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131Hirokazu Tamamura, Kenichi Hiramatsu, Satoshi Ueda, et al.
Journal of Medicinal Chemistry|April 29, 2005
Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide scaffoldsHirokazu Tamamura, Takanobu Araki, Satoshi Ueda, et al.
Pageof 13

Showing results (101-110 of 123) with videos related to

Sort By:
Pageof 13
The Journal of Endocrinology|January 14, 2025
Effects of tryptophan-selective lipidated glucagon-like peptide 1 (GLP-1) peptides on the GLP-1 receptorXuejing Lu, Norio Harada, Takuma Yasuda, et al.
Bioorganic & Medicinal Chemistry Letters|October 26, 2005
Design and synthesis of downsized metastin (45-54) analogs with maintenance of high GPR54 agonistic activityAyumu Niida, Zixuan Wang, Kenji Tomita, et al.
The Journal of Biological Chemistry|February 18, 2006
Specific recognition of the collagen triple helix by chaperone HSP47. II. The HSP47-binding structural motif in collagens and related proteinsTakaki Koide, Yoshimi Nishikawa, Shinichi Asada, et al.
Journal of Medicinal Chemistry|April 18, 2003
Reduction of peptide character of HIV protease inhibitors that exhibit nanomolar potency against multidrug resistant HIV-1 strainsHirokazu Tamamura, Yasuhiro Koh, Satoshi Ueda, et al.
Organic & Biomolecular Chemistry|May 9, 2014
Development of a traceable linker containing a thiol-responsive amino acid for the enrichment and selective labelling of target proteinsJun Yamamoto, Masaya Denda, Nami Maeda, et al.
Angewandte Chemie (International Ed. in English)|February 25, 2021
Discovery of a Macropinocytosis-Inducing Peptide Potentiated by Medium-Mediated Intramolecular Disulfide FormationJan Vincent V Arafiles, Hisaaki Hirose, Yusuke Hirai, et al.
The Journal of Organic Chemistry|May 6, 2006
Stereoselective synthesis of 3,6-disubstituted-3,6-dihydropyridin-2-ones as potential diketopiperazine mimetics using organocopper-mediated anti-SN2' reactions and their use in the preparation of low-molecule CXCR4 antagonistsAyumu Niida, Hiroaki Tanigaki, Eriko Inokuchi, et al.
Organic & Biomolecular Chemistry|December 3, 2003
Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivativesHirokazu Tamamura, Kenichi Hiramatsu, a Shuichi Kusano, et al.
Journal of Medicinal Chemistry|January 22, 2005
Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131Hirokazu Tamamura, Kenichi Hiramatsu, Satoshi Ueda, et al.
Journal of Medicinal Chemistry|April 29, 2005
Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide scaffoldsHirokazu Tamamura, Takanobu Araki, Satoshi Ueda, et al.
Pageof 13