{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,26]],"date-time":"2026-10-26T21:19:45Z","timestamp":1793049585283,"version":"4.5.0"},"reference-count":55,"publisher":"MDPI AG","issue":"6","license":[{"start":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T00:00:00Z","timestamp":1780358400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Ministry of Science and Higher Education of the Republic of Kazakhstan","award":["AP23489639"],"award-info":[{"award-number":["AP23489639"]}]},{"award":["AP23489639"],"award-info":[{"award-number":["AP23489639"]}],"id":[{"id":"https:\/\/ror.org\/05tyne317","id-type":"ROR","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pharmaceuticals"],"abstract":"<jats:p>Background\/Objectives: For the first time, water-soluble encapsulated forms of 20-hydroxyecdysone were synthesized as clathrate complexes with \u03b2-cyclodextrin. The derivatives included a ketoxime form (20-NOH), obtained by selective oximation of the C-6 carbonyl, and a triacetate form (3Ac-20E), obtained by regioselective acetylation of the C-2, C-3, and C-22 hydroxyl groups. Methods: The chemical structures of the obtained compounds were confirmed using spectroscopic methods, including 1H and 13C NMR. The Z-configuration of the oxime in 20-NOH was established by the diagnostic upfield shift in the C-5 resonance (\u03b4 36.0 ppm) relative to the parent compound (\u03b4 51.4 ppm). Results: The antioxidant activity was evaluated using FRAP and DPPH assays. The \u03b2-cyclodextrin complexes were shown to exhibit significantly higher radical scavenging activity, with IC50 values of &lt;0.05 mg\/mL compared to 0.24 mg\/mL for the parent 20-hydroxyecdysone (20E). In the FRAP assay, the complexes demonstrated enhanced reducing capacity, with values of 3.452 \u00b1 0.520 AAE\/mL for the ketoxime form (20-NOH\u00b7\u03b2-CD) at a concentration of 0.75 mg\/mL and 3.810 \u00b1 0.279 AAE\/mL for the acetate form (3Ac-20E\u00b7\u03b2-CD) at the same concentration, whereas the parent compound did not exceed 0.46 AAE\/mL. In both in vitro and in vivo experiments, it was established that the investigated complexes demonstrated hepatoprotective properties, as evidenced by the normalization of biochemical parameters as well as the restoration of liver structure according to ultrasound and histological studies. The ketoxime-derived complex (20-NOH\u00b7\u03b2-CD) at a dose of 25 mg\/kg demonstrates the greatest reduction in transaminase activity and MDA levels, indicating its high efficacy and the presence of an optimal therapeutic dose. In addition, the encapsulated forms demonstrated moderate antifungal activity against Candida albicans and bactericidal activity against four bacterial strains (MIC &gt;10 mg\/mL). Conclusions: The obtained results indicate that \u03b2-cyclodextrin complexes significantly enhance the biological activity of 20E and highlight the potential of these compounds for pharmaceutical applications.<\/jats:p>","DOI":"10.3390\/ph19060885","type":"journal-article","created":{"date-parts":[[2026,6,4]],"date-time":"2026-06-04T01:08:02Z","timestamp":1780535282000},"page":"885","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["\u03b2-Cyclodextrin Inclusion Complexes of 20-Hydroxyecdysone Derivatives: Synthesis, NMR Characterization, and In Vitro\/In Vivo Evaluation of Antioxidant, Hepatoprotective, and Antimicrobial Activities"],"prefix":"10.3390","volume":"19","author":[{"given":"Borash","family":"Tuleuov","sequence":"first","affiliation":[{"name":"Laboratory of Chemistry of Steroid Compounds, JSC \u201cScientific and Production Center \u201cPhytochemistry\u201d, Karaganda 100009, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0003-3586-8248","authenticated-orcid":false,"given":"Aizhan","family":"Zeinuldina","sequence":"additional","affiliation":[{"name":"Department of General and Biological Chemistry, Astana Medical University, Astana 010000, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3584-9544","authenticated-orcid":false,"given":"Aidana","family":"Bazarkhankyzy","sequence":"additional","affiliation":[{"name":"Department of General and Biological Chemistry, Astana Medical University, Astana 010000, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1048-9749","authenticated-orcid":false,"given":"Aizhan","family":"Kozhanova","sequence":"additional","affiliation":[{"name":"Laboratory of Chemistry of Steroid Compounds, JSC \u201cScientific and Production Center \u201cPhytochemistry\u201d, Karaganda 100009, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bakhtiyar","family":"Temirgaziyev","sequence":"additional","affiliation":[{"name":"Laboratory of Chemistry of Steroid Compounds, JSC \u201cScientific and Production Center \u201cPhytochemistry\u201d, Karaganda 100009, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6537-3324","authenticated-orcid":false,"given":"Saniya","family":"Dyussekeyeva","sequence":"additional","affiliation":[{"name":"Department of General and Biological Chemistry, Astana Medical University, Astana 010000, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lyazzat","family":"Abulyaissova","sequence":"additional","affiliation":[{"name":"Department of Physical and Analytical Chemistry, Buketov Karaganda University, Karaganda 100028, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8796-0108","authenticated-orcid":false,"given":"Nurgul","family":"Askarova","sequence":"additional","affiliation":[{"name":"Department of General and Biological Chemistry, Astana Medical University, Astana 010000, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8131-0390","authenticated-orcid":false,"given":"Aliya","family":"Temirbekova","sequence":"additional","affiliation":[{"name":"Laboratory of Microbiology, Republican Collection of Microorganisms LPP, Astana 010000, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5855-2655","authenticated-orcid":false,"given":"Zhanar","family":"Tekebayeva","sequence":"additional","affiliation":[{"name":"Laboratory of Microbiology, Republican Collection of Microorganisms LPP, Astana 010000, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7038-1740","authenticated-orcid":false,"given":"Ardak","family":"Sapiyeva","sequence":"additional","affiliation":[{"name":"Department of General and Biological Chemistry, Astana Medical University, Astana 010000, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7588-6174","authenticated-orcid":false,"given":"Sergazy","family":"Adekenov","sequence":"additional","affiliation":[{"name":"Laboratory of Chemistry of Steroid Compounds, JSC \u201cScientific and Production Center \u201cPhytochemistry\u201d, Karaganda 100009, Kazakhstan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2026,6,2]]},"reference":[{"key":"ref_1","unstructured":"Kurakina, I.O., and Bulaev, V.N. 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