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Isolation, synthesis and bioactivity studies of phomactin terpenoids
- Source :
- Nature Chemistry. 10:938-945
- Publication Year :
- 2018
- Publisher :
- Springer Science and Business Media LLC, 2018.
-
Abstract
- Studies of secondary metabolites (natural products) that cover their isolation, chemical synthesis and bioactivity investigation present myriad opportunities for discovery. For example, the isolation of novel secondary metabolites can inspire advances in chemical synthesis strategies to achieve their practical preparation for biological evaluation. In the process, chemical synthesis can also provide unambiguous structural characterization of the natural products. Although the isolation, chemical synthesis and bioactivity studies of natural products are mutually beneficial, they are often conducted independently. Here, we demonstrate the benefits of a collaborative study of the phomactins, diterpenoid fungal metabolites that serve as antagonists of the platelet activating factor receptor. Our isolation of novel phomactins has spurred the development of a bioinspired, unified approach that achieves the total syntheses of six congeners. We also demonstrate in vitro the beneficial effects of several phomactins in suppressing the rate of repopulation of tumour cells following gamma radiation therapy.
- Subjects :
- Cell Survival
General Chemical Engineering
Platelet Membrane Glycoproteins
010402 general chemistry
01 natural sciences
Chemical synthesis
Receptors, G-Protein-Coupled
Inhibitory Concentration 50
Structure-Activity Relationship
Cell Line, Tumor
Humans
Structure–activity relationship
Inhibitory concentration 50
Beneficial effects
Biological evaluation
Biological Products
Terpenes
010405 organic chemistry
Chemistry
Fungi
Stereoisomerism
General Chemistry
Isolation (microbiology)
Terpenoid
0104 chemical sciences
Biochemistry
Gamma Rays
Repopulation
Subjects
Details
- ISSN :
- 17554349 and 17554330
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Nature Chemistry
- Accession number :
- edsair.doi.dedup.....4334e11b9a97b548a979d9976042f662