Facile Formation of Chiral Calixarene Analogs Incorporating Cystine Peptide into the Macrocyclic Ring.
スポンサーリンク
概要
- 論文の詳細を見る
Chiral calixarene analogs incorporating cystine peptide into their macrocyclic ring were easily prepared by the cyclization reactions of bis(chloromethyl)phenol-formaldehyde oligomers with cystine peptides in moderate yields. Circular dichroism (CD) spectra indicated the existence of the transmission of the chirality from peptide unit to phenol-formaldehyde oligomer moiety
- 公益社団法人日本薬学会の論文
- 2002-03-01
著者
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Watanabe Kazuhito
Department of Hygienic Chemistry, Faculty of Pharmaceutical Sciences, Hokuriku University
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OHBA Yoshihiro
Department of Human Sensing and Functional Sensor Engineering, Graduate School of Engineering, Yamag
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Itoh K
Drug Formulation Research Laboratories Phaemaceutical Research Institute Kyowa Hakko Kogyo Co. Ltd.
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Ito Kunio
Pharmaceutical Research Laboratories Kyowa Hakko Kogyo Co. Ltd.
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Watanabe Kazuhito
Department Of Chemistry And Chemical Engineering Faculty Of Engineering Yamagata University
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Tai Takaaki
Morishita Jintan Co. Ltd.
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Tamura T
Department Of Chemistry And Chemical Engineering Faculty Of Engineering Yamagata University
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Ohba Y
Toshiba Corp. Kawasaki Jpn
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Ohba Y
Yamagata Univ. Yonezawa Jpn
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Ohba Yoshihiro
Department Of Chemistry And Chemical Engineering Faculty Of Engineering Yamagata University
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ITO Kazuaki
Department of Chemistry and Chemical Engineering, Faculty of Engineering, Yamagata University
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TAMURA Takafumi
Department of Chemistry and Chemical Engineering, Faculty of Engineering, Yamagata University
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Ito K
Janssen Pharmaceutical K.k. Shizuoka Jpn
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Ito Kazuaki
Department Of Chemistry And Chemical Engineering Faculty Of Engineering Yamagata University
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Ito Kazuaki
Department Of Applied Chemistry Nagoya Institute Of Technology
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Tamura Tkahumi
Department of Chemistry and Chemical Engineering, Faculty of Engineering, Yamagata University
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Ohba Yoshihiro
Department of Applied Chemistry, Faculty of Engineering, Yamagata University
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