@article{oai:kumadai.repo.nii.ac.jp:00027691,
 author = {横手, さわな and 清水, 英介 and 川原, 浩一 and 國安, 明彦 and 白﨑, 哲哉 and 高濱, 和夫 and Takahama, Kazuo and 紺野, 勝弘 and 川合, 述史 and 山岡, 薫 and 木下, 英司 and 中山, 仁 and Yokote, Sawana and Setoguchi, Ritsuko and Shimizu, Eisuke and Mishima, Naoki and Kawahara, Kohichi and Kuniyasu, Akihiko and 白崎, 哲哉 and Shirasaki, Tetsuya and 高濱, 和夫 and Takahama, Kazuo and Konno, Katsuhiro and Kawai, Nobufumi and Yamaoka, Kaoru and Kinoshita, Eiji and 中山, 仁 and Nakayama, Hitoshi},
 issue = {1},
 journal = {Heterocycles},
 month = {Dec},
 note = {application/pdf, 論文(Article), To develop inhibitors that are selective for brain-type sodium channels, several peptides were synthesized on the basis of pompilidotoxin structure. A peptide having N-terminal 7 amino acids and its homologs in which Phe7 is substituted into more hydrophobic amino acids, selectively inhibit sodium current of brain-type sodium channels., http://www.heterocycles.jp/newlibrary/libraries/abst/20362},
 pages = {925--933},
 title = {A synthetic approach to develop peptide inhibitors selective for brain-type sodium channels on the basis of pompilidotoxin structure},
 volume = {79},
 year = {2008},
 yomi = {タカハマ, カズオ and シラサキ, テツヤ and タカハマ, カズオ and ナカヤマ, ヒトシ}
}