๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Jasplakinolide, a cyclodepsipeptide from the marine sponge, Jaspis SP.

โœ Scribed by Phillip Crews; Lawrence V Manes; Mark Boehler


Book ID
104218727
Publisher
Elsevier Science
Year
1986
Tongue
French
Weight
295 KB
Volume
27
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


A practical synthesis of the peptide par
โœ Shinji Kato; Yasumasa Hamada; Takayuki Shioiri ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 163 KB

S)-Alanyl-(R)-2-bromoabryl-(R)-P-tyrosine found in jaspamide(1) was conveniently synthesized as its protected derivative 2 in good yield. Jaspamide (jasplakinolide)(l)s recently isolated from a jaspis sponge is a novel cyclodepsipeptide exhibiting potent insecticidal and antifungal activities. Recen

Jaspamide from the Marine Sponge Jaspis
โœ Braekman, J. C.; Daloze, D.; Moussiaux, B.; Riccio, R. ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› American Chemical Society ๐ŸŒ English โš– 155 KB
Geodiamolides H and I, further cyclodeps
โœ Winston F. Tinto; Alan J. Lough; Stewart McLean; William F. Reynolds; Margaret Y ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 326 KB

Two new cyclodepsipeptides, geodiamolide H (3) and I (4), were isolated from the marine sponge Geodia sp. The structures of 3 and 4 were determined by 2D NMR spectroscopy while the absolute stereochemistry of 4 was established by X-ray crystallography. Geodiamolide H 3 was cytotoxic to some human ca