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Additional Insights into the Obtusallene Family: Components of Laurencia marilzae
- Source :
- Journal of Natural Products, Journal of Natural Products, American Chemical Society, 2016, 79 (4), pp.1184-1188. ⟨10.1021/acs.jnatprod.5b01080⟩
- Publication Year :
- 2016
- Publisher :
- HAL CCSD, 2016.
-
Abstract
- The obtusallenes are a significant subset of C15-halogenated acetogenins that incorporate 12-membered cyclic ethers. We have recently reported the isolation from Laurencia marilzae of 12-epoxyobtusallene IV (1) and its related α,β-unsaturated carboxylate ester (2), both of special biogenetic relevance. Here we describe the final step of our study, the isolation of three new analogues (3-5), among these, the first bromopropargylic derivative (3) of this class of macrocyclic C15-acetogenins. The structures were elucidated by analysis of NMR and X-ray data. 12-Epoxyobtusallene IV (1), its new isomer 4, and known obtusallene IV (6) were evaluated for their apoptosis-inducing activities in a human hepatocarcinoma cell line.
- Subjects :
- Carcinoma, Hepatocellular
Acetogenins
Stereochemistry
Molecular Conformation
Pharmaceutical Science
Antineoplastic Agents
Apoptosis
[SDV.CAN]Life Sciences [q-bio]/Cancer
Crystallography, X-Ray
010402 general chemistry
Laurencia
01 natural sciences
Molecular conformation
Analytical Chemistry
chemistry.chemical_compound
Ethers, Cyclic
Drug Discovery
Humans
Carboxylate
ComputingMilieux_MISCELLANEOUS
Pharmacology
Molecular Structure
biology
010405 organic chemistry
Laurencia marilzae
Organic Chemistry
[SDV.MHEP.HEG]Life Sciences [q-bio]/Human health and pathology/Hépatology and Gastroenterology
biology.organism_classification
Hydrocarbons, Brominated
3. Good health
0104 chemical sciences
Complementary and alternative medicine
chemistry
Spain
Obtusallene
[SDV.SP.PHARMA]Life Sciences [q-bio]/Pharmaceutical sciences/Pharmacology
Molecular Medicine
Derivative (chemistry)
Subjects
Details
- Language :
- English
- ISSN :
- 01633864 and 15206025
- Database :
- OpenAIRE
- Journal :
- Journal of Natural Products, Journal of Natural Products, American Chemical Society, 2016, 79 (4), pp.1184-1188. ⟨10.1021/acs.jnatprod.5b01080⟩
- Accession number :
- edsair.doi.dedup.....81e63ebba668238e0f6ac96ca8500949
- Full Text :
- https://doi.org/10.1021/acs.jnatprod.5b01080⟩