Single- and double-chained truncated jaspine B analogues: asymmetric synthesis, biological evaluation and theoretical study of an unexpected 5-endo-dig process-Reference-Cited by-同舟云学术

Single- and double-chained truncated jaspine B analogues: asymmetric synthesis, biological evaluation and theoretical study of an unexpected 5-endo-dig process

Published:2011-06 Issue:23 Volume:67 Page:4253-4262
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Salma Yahya,Ballereau Stéphanie,Ladeira Sonia,Lepetit Christine,Chauvin Remi,Andrieu-Abadie Nathalie,Génisson Yves

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference37 articles.

1. Jaspines A and B: two new cytotoxic sphingosine derivatives from the marine sponge Jaspis sp.

2. Pachastrissamine, a Cytotoxic Anhydrophytosphingosine from a Marine Sponge, Pachastrissa sp.

3. Synthesis and biological properties of Pachastrissamine (jaspine B) and diastereoisomeric jaspines

4. The natural marine anhydrophytosphingosine, Jaspine B, induces apoptosis in melanoma cells by interfering with ceramide metabolism

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