CAS 469-06-7
:(3R,6E,22E)-9,10-secoergosta-5(10),6,8(14),22-tetraen-3-ol
Description:
The chemical substance known as (3R,6E,22E)-9,10-secoergosta-5(10),6,8(14),22-tetraen-3-ol, with the CAS number 469-06-7, is a sterol derivative that plays a significant role in biological systems, particularly in the context of plant and fungal biochemistry. This compound features a complex polycyclic structure characterized by multiple double bonds and a hydroxyl group, which contributes to its reactivity and interaction with biological membranes. Its stereochemistry, indicated by the (3R,6E,22E) configuration, suggests specific spatial arrangements that can influence its biological activity and function. As a seco-steroid, it is derived from the degradation of sterols and is involved in various metabolic pathways. This compound is of interest in research related to phytochemistry and pharmacology, as it may exhibit potential health benefits or biological activities, including antifungal or anti-inflammatory properties. Its unique structural features make it a subject of study in the synthesis of novel compounds and understanding the biochemical roles of sterols in living organisms.
Formula:C28H44O
InChI:InChI=1/C28H44O/c1-19(2)20(3)9-10-22(5)26-15-16-27-23(8-7-17-28(26,27)6)12-13-24-18-25(29)14-11-21(24)4/h9-10,12-13,19-20,22,25-26,29H,7-8,11,14-18H2,1-6H3/b10-9+,13-12+/t20-,22+,25+,26+,28+/m0/s1
Sort by
The purity filter is not visible because current products do not have associated purity data for filtering.
Found 3 products.
Isotachysterol
CAS:Controlled Product<p>Stability Light Sensitive, Temperature Sensitive, Toxic<br>Applications A vitamin D analog.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Seamark, D.A., et al.: J. Steroid Biochem., 13, 1057 (1980),<br></p>Formula:C28H44OColor and Shape:NeatMolecular weight:396.65
