𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis, Conformational Analysis, and Cytotoxicity of New Analogues of the Natural Cyclodepsipeptide Jaspamide †

✍ Scribed by Terracciano, Stefania; Bruno, Ines; Bifulco, Giuseppe; Copper, Jean E.; Smith, Charles D.; Gomez-Paloma, Luigi; Riccio, Raffaele

Book ID
127091115
Publisher
American Chemical Society
Year
2004
Tongue
English
Weight
143 KB
Volume
67
Category
Article
ISSN
0163-3864

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and Structure–Activity Relatio
Synthesis and Structure–Activity Relationship of Cytotoxic Marine Cyclodepsipeptide IB-01212 Analogues
✍ Luis J. Cruz; Andres Francesch; Carmen Cuevas; Fernando Albericio 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 217 KB 👁 1 views

## Abstract Several recently discovered marine products have remarkable in vitro and in vivo anticancer profiles against a wide range of tumor cell lines. Some of these compounds are currently in clinical trials. These compounds show complex structures and mechanisms of action of interest. Herein,

Synthesis and Conformational Analysis of
Synthesis and Conformational Analysis of Geodiamolide Analogues
✍ Srinivasa Marimganti; Ralph Wieneke; Armin Geyer; Martin E. Maier 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 265 KB 👁 2 views

## Abstract Starting with the ω‐hydroxy and ω‐amino acid derivatives **13** and **21**, the two closely related geodiamolide analogs **32** and **35**, respectively, were prepared. Compared to the natural cyclodepsipeptide geodiamolide (**1**), the macrocycles **32** and **35** have a smaller ring

Synthesis and conformational analysis of
Synthesis and conformational analysis of apamin analogues with natural and non-natural cystine/selenocystine connectivities
✍ Stella Fiori; Stefano Pegoraro; Sabine Rudolph-Böhner; Jörg Cramer; Luis Moroder 📂 Article 📅 2000 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 307 KB 👁 2 views

By replacing two cysteine residues in apamin with selenocysteine, the three possible isomers related to the side-chain connectivities of a bis-cystinyl-peptide were synthesized in regioselective manner exploiting the low redox potential of the diselenide bond. Nuclear magnetic resonance conformation