抄録
In order to produce stable analogs in blood of arenastatin A, a potent cytotoxic depsipeptide from the marine sponge Dysidea arenaria, we synthesized four analogs in which the 15-20 ester linkage was modified. Among them, the carba analog and 20-deoxo analog showed stability in serum. The conformation of arenastatin A and its three analogs were analyzed by distance-restrained molecular dynamic calculation to elucidate a three-dimensional stereostructure contributing to the extremely potent cytotoxicity of arenastatin A.
本文言語 | English |
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ページ(範囲) | 4323-4336 |
ページ数 | 14 |
ジャーナル | Tetrahedron |
巻 | 57 |
号 | 20 |
DOI | |
出版ステータス | Published - 2001 5 14 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry