Abstract:
:20-Hydroxyecdysterone - (2β,3β,5β,22R)-2,3,14,20,22,25-hexahydroxycholest-7-en-6-one was isolated in satisfactory yield using ethanol extraction from the aerial part of Silene wolgensis (Hornem.) Otth; sometimes Silene wolgensis (Willd.) Bess. ex Spreng. The complexation of the phytoecdysteroid with β-cyclodextrin was studied by NMR spectroscopy. By studying the changes in chemical shifts of protons of substrates and receptors it was found that ecdysterone interacts with cyclodextrins to form supramolecular inclusion complexes of stoichiometric composition of 1:1 or 1:2. Ecdysterone-β-cyclodextrin complexes exhibit 100 times higher solubility in water than the parent compound.
journal_name
Steroidsjournal_title
Steroidsauthors
Temirgaziyev BS,Kučáková K,Baizhigit YA,Jurášek M,Džubák P,Hajdúch M,Dolenský B,Drašar PB,Tuleuov BI,Adekenov SMdoi
10.1016/j.steroids.2018.11.007subject
Has Abstractpub_date
2019-07-01 00:00:00pages
37-41eissn
0039-128Xissn
1878-5867pii
S0039-128X(18)30211-3journal_volume
147pub_type
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