Enantiomer-Differentiating Ability of Cyclo(L-Phe-L-Pro)4 Having a Rigid Skeleton for Phenylalanine Methylester Hydrochloride.

• ISHIZU Takashi

• NOGUCHI Shunsaku

書誌事項

タイトル別名

• Enantiomer-Differentiating Ability of C

抄録

The formation constant of the 1 : 1 complex of cyclo(L-Phe-L-Pro)₄ (1) with L-PheOMe·HCl was about 13.2 times that of the complex with D-PheOMe·HCl. The 1 : 1 complex of 1 with L-PheOMe·HCl formed three intermolecular hydrogen bonds between Pro² CO, Phe¹ CO and the amino group, and Phe² NH and the carbonyl group, whereas that with D-PheOMe·HCl formed only one between Phe¹ CO and the amino group.

収録刊行物

• ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ

  ＣＨＥＭＩＣＡＬ　＆　ＰＨＡＲＭＡＣＥＵＴＩＣＡＬ　ＢＵＬＬＥＴＩＮ 45 (7), 1202-1204, 1997

  公益社団法人 日本薬学会

キーワード

• cyclopeptide
• chiral recognition
• hydrogen bond
• NMR
• formation constant

詳細情報

• CRID: 1390001204159372032
• NII論文ID: 130003947313
• NII論文ID: 110003616640
• NII書誌ID: AA00602100
• DOI: 10.1248/cpb.45.1202
• ISSN: 13475223
• ISSN: 00092363
• NDL書誌ID: 4260333
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I4260333
• Web Site: http://www.jstage.jst.go.jp/article/cpb1958/45/7/45_7_1202/_pdf
• 本文言語コード: en
• データソース種別:
  • JaLC
  • NDL
  • Crossref
  • CiNii Articles
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