Studies on the constituents of marine opisthobranchia, II. Structures of the new diacylglyceryl ether and cholesteryl ester mixture, and of three nucleosides from fertilized eggs of the sea hare Aplysia kurodai

Tomofumi Miyamoto, Ryuichi Higuchi, Misa Funatsu, Haruko Seike, Toshihiro Nohara, Tetsuya Komori

研究成果: ジャーナルへの寄稿記事

5 引用 (Scopus)

抄録

From freshly fertilized eggs of the sea hare Aplysia kurodai, collected in Fukuoka Prefecture, the new laxative lipid, the diacylglyceryl ether mixture (1) and cholesteryl ester mixture (2), in addition to the three nucleosides 4, 5, and 6, have been isolated. The structures of 1 and 2 were elucidated on the basis of chemical and spectral evidence. The nucleosides 4, 5, and 6 have been identified as 1‐(2‐deoxy‐β‐D‐ribofuranosyl)thymine, adenosine, and inosine, respectively.

元の言語英語
ページ(範囲)585-587
ページ数3
ジャーナルLiebigs Annalen der Chemie
1988
発行部数6
DOI
出版物ステータス出版済み - 1 1 1988

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nucleosides
eggs
Nucleosides
esters
ethers
adenosines
Inosine
Laxatives
Thymine
thymine
Cholesterol Esters
Ether
Adenosine
lipids
Lipids
cholesteryl 5-carboxypentyl ether N-hydroxysuccinimide ester

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Organic Chemistry

これを引用

Studies on the constituents of marine opisthobranchia, II. Structures of the new diacylglyceryl ether and cholesteryl ester mixture, and of three nucleosides from fertilized eggs of the sea hare Aplysia kurodai. / Miyamoto, Tomofumi; Higuchi, Ryuichi; Funatsu, Misa; Seike, Haruko; Nohara, Toshihiro; Komori, Tetsuya.

:: Liebigs Annalen der Chemie, 巻 1988, 番号 6, 01.01.1988, p. 585-587.

研究成果: ジャーナルへの寄稿記事

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abstract = "From freshly fertilized eggs of the sea hare Aplysia kurodai, collected in Fukuoka Prefecture, the new laxative lipid, the diacylglyceryl ether mixture (1) and cholesteryl ester mixture (2), in addition to the three nucleosides 4, 5, and 6, have been isolated. The structures of 1 and 2 were elucidated on the basis of chemical and spectral evidence. The nucleosides 4, 5, and 6 have been identified as 1‐(2‐deoxy‐β‐D‐ribofuranosyl)thymine, adenosine, and inosine, respectively.",
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