3577-13-7
Chemical Structure
β-Sitosteryl linoleate
- CAS. Nr.: 3577-13-7
- Formula:C47H80O2
- Molecular Weight:677.14
InChIKey: TXNOTJVZNDGTOR-DCBLFMKISA-N
SMILES: C[C@@]12[C@]3([H])[C@](CC=C1C[C@H](CC2)OC(CCCCCCC/C=C\C/C=C\CCCCC)=O)([H])[C@@]4([H])[C@](CC3)([C@@](CC4)([H])[C@H](C)CC[C@@H](CC)C(C)C)C
Biological Activity:
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
β-Sitosteryl linoleate | β-Sitosteryl linoleate is an antifungal agent with a MIC of 500 μg/mL against Alternaria alternata. β-Sitosteryl linoleate disrupts the mycelia of A. alternata and causes leakage of cellular contents. β-Sitosteryl linoleate can be used in studies on A. alternata-related fungal infections, Alternaria brown spot and the mechanisms of phytopathogenic fungi, as well as in GC/MS analytical studies of steryl esters. |
|||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Hammann S, et al. Gas chromatographic separation of fatty acid esters of cholesterol and phytosterols on an ionic liquid capillary column. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2015 Dec 15;1007:67-71.
- [2]. Campos VA, et al. Anadenanthera colubrina (Vell.) Brenan produces steroidal substances that are active against Alternaria alternata (Fr.) Keissler and that may bind to oxysterol-binding proteins. Pest management science. 2014 Dec;70(12):1815-22.
Keywords