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Syntheses and Biological Activities of Danicalipin A Derivatives.
Umezawa, Taiki; Maeda, Takeshi; Akiyama, Takuya; Iman Prakoso, Nurcahyo; Jerin Mehjabin, Jakia; Okino, Tatsufumi; Matsuda, Fuyuhiko.
Afiliação
  • Umezawa T; Graduate School of Environmental Science, Hokkaido University, N10W5, Sapporo, 060-0810, Japan.
  • Maeda T; Graduate School of Environmental Science, Hokkaido University, N10W5, Sapporo, 060-0810, Japan.
  • Akiyama T; Graduate School of Environmental Science, Hokkaido University, N10W5, Sapporo, 060-0810, Japan.
  • Iman Prakoso N; Graduate School of Environmental Science, Hokkaido University, N10W5, Sapporo, 060-0810, Japan.
  • Jerin Mehjabin J; Chemistry Department, Universitas Islam Indonesia, Sleman, Yogyakarta, Indonesia.
  • Okino T; Graduate School of Environmental Science, Hokkaido University, N10W5, Sapporo, 060-0810, Japan.
  • Matsuda F; Graduate School of Environmental Science, Hokkaido University, N10W5, Sapporo, 060-0810, Japan.
Chem Biodivers ; 20(6): e202300400, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37073090
Synthesis of three derivatives of danicalipin A, tetrachloride, trisulfate and a fluorescent probe was achieved through Wittig reaction strategy. Toxicity of the derivatives against brine shrimp (Artemia salina) as also investigated to provide useful information for the biological activity; i) less chloride derivative showed similar toxicity to danicalipin A, ii) the amphiphilic property, a characteristic feature of danicalipin A, was crucial because trisulfate considerably decreased the toxicity and iii) fluorescent derivative kept brine shrimp toxicity of danicalipin A.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article