Inclusion complexes of 2-methoxyestradiol with dimethylated and permethylated β-cyclodextrins: models for cyclodextrin–steroid interaction

Scholarly Works

• Szente, L.; Tuza, K.; Herr, D. M.; Varga, E.; Szőcs, L.; Fenyvesi, É.; Puskás, I. Rapid test for identification of heptakis (2,6-di-O-methyl) β-cyclodextrin in isomeric mixtures. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2025. doi:10.1007/s10847-025-01304-1
• Anderson, A.; Piñeiro, Á.; García-Fandiño, R.; O'Connor, M. S. Cyclodextrins: Establishing building blocks for AI-driven drug design by determining affinity constants in silico. Computational and structural biotechnology journal 2024, 23, 1117–1128. doi:10.1016/j.csbj.2024.02.011
• Georgiou, N.; Kakava, M. G.; Routsi, E. A.; Petsas, E.; Stavridis, N.; Freris, C.; Zoupanou, N.; Moschovou, K.; Kiriakidi, S.; Mavromoustakos, T. Quercetin: A Potential Polydynamic Drug. Molecules (Basel, Switzerland) 2023, 28, 8141. doi:10.3390/molecules28248141
• Araj, S. K.; Szeleszczuk, Ł. A Review on Cyclodextrins/Estrogens Inclusion Complexes. International journal of molecular sciences 2023, 24, 8780. doi:10.3390/ijms24108780
• Vicatos, A. I.; Hoossen, Z.; Caira, M. R. Inclusion complexes of the steroid hormones 17β-estradiol and progesterone with β- and γ-cyclodextrin hosts: syntheses, X-ray structures, thermal analyses and API solubility enhancements. Beilstein journal of organic chemistry 2022, 18, 1749–1762. doi:10.3762/bjoc.18.184
• Dohle, W.; Asiki, H.; Gruchot, W.; Foster, P. A.; Sahota, H. K.; Bai, R.; Christensen, K. E.; Hamel, E.; Potter, B. V. L. 2-Difluoromethoxy-Substituted Estratriene Sulfamates: Synthesis, Antiproliferative SAR, Antitubulin Activity, and Steroid Sulfatase Inhibition. ChemMedChem 2022, 17, e202200408. doi:10.1002/cmdc.202200408
• Giri, B. R.; Yang, H. S.; Song, I.-S.; Choi, H.-G.; Cho, J. H.; Kim, D. W. Alternative Methotrexate Oral Formulation: Enhanced Aqueous Solubility, Bioavailability, Photostability, and Permeability. Pharmaceutics 2022, 14, 2073. doi:10.3390/pharmaceutics14102073
• Vicatos, A. I.; Caira, M. R. Cyclodextrin complexes of the anticonvulsant agent valproic acid. CrystEngComm 2021, 23, 6582–6590. doi:10.1039/d1ce01024g
• Mahalapbutr, P.; Charoenwongpaiboon, T.; Phongern, C.; Kongtaworn, N.; Hannongbua, S.; Rungrotmongkol, T. Molecular encapsulation of a key odor-active 2-acetyl-1-pyrroline in aromatic rice with β-cyclodextrin derivatives. Journal of Molecular Liquids 2021, 337, 116394. doi:10.1016/j.molliq.2021.116394
• Anderson, A. M.; Kirtadze, T.; Malanga, M.; Dinh, D.; Barnes, C.; Campo, A.; Clemens, D. M.; García-Fandiño, R.; Piñeiro, Á.; O'Connor, M. S. Cyclodextrin dimers: A versatile approach to optimizing encapsulation and their application to therapeutic extraction of toxic oxysterols. International journal of pharmaceutics 2021, 606, 120522. doi:10.1016/j.ijpharm.2021.120522
• Belyakova, L. A. Капсулювання бензолкарбонових кислот за допомогою циклодекстринів. Himia, Fizika ta Tehnologia Poverhni 2021, 12, 40–51. doi:10.15407/hftp12.01.040
• Giri, B. R.; Lee, J.; Lim, D. Y.; Kim, D. W. Docetaxel/dimethyl-β-cyclodextrin inclusion complexes: preparation, in vitro evaluation and physicochemical characterization. Drug development and industrial pharmacy 2021, 47, 319–328. doi:10.1080/03639045.2021.1879840
• Mojdehi, M. F. P.; Koli, M. G.; Bolagh, M. D. O.; Gardeh, M. G.; Hashemianzadeh, S. M. A detailed computational study on binding of kinase inhibitors into β-cyclodextrin: inclusion complex formation. Molecular Systems Design & Engineering 2021, 6, 80–92. doi:10.1039/d0me00140f
• Wang, C.; Yang, R.; Zhang, B.; Rongxia, Q.; Liu, H. The apparent formation constants of asiatic acid and its derivatives existing in Centella asiatica with cyclodextrins by HPLC. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2020, 98, 261–270. doi:10.1007/s10847-020-01026-6
• Barton, B.; Jooste, D. V.; Senekal, U.; Hosten, E. C. Four xanthenyl-derived compounds: a comparative investigation of their host behaviour in the presence potential saturated and unsaturated heterocyclic six-membered ring guest solvents. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2020, 97, 217–229. doi:10.1007/s10847-020-00997-w
• Kučáková, K.; Dolenský, B. Molecular structure study of a heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin complex of cholesterol. Steroids 2019, 155, 108555. doi:10.1016/j.steroids.2019.108555
• Caira, M. R. Cyclodextrin Inclusion of Medicinal Compounds for Enhancement of their Physicochemical and Biopharmaceutical Properties. Current topics in medicinal chemistry 2019, 19, 2357–2370. doi:10.2174/1568026619666191018101524
• Lobatto, V. L.; Argüello, G. A.; Caira, M. R.; Buján, E. I. Trifluralin and two of its photodegradation products: Crystal structures and phase solubility/UV studies with cyclodextrins. Journal of Physical Organic Chemistry 2019, 32. doi:10.1002/poc.4006
• Lavorgna, M.; Iacovino, R.; Russo, C.; Di Donato, C.; Piscitelli, C.; Isidori, M. A New Approach for Improving the Antibacterial and Tumor Cytotoxic Activities of Pipemidic Acid by Including It in Trimethyl-β-cyclodextrin. International journal of molecular sciences 2019, 20, 416. doi:10.3390/ijms20020416
• Furlan, A. L.; Buchoux, S.; Miao, Y.; Banchet, V.; Létévé, M.; Lambertyn, V.; Michel, J.; Sarazin, C.; Bonnet, V. Nanoparticles based on lipidyl-β-cyclodextrins: synthesis, characterization, and experimental and computational biophysical studies for encapsulation of atazanavir. New Journal of Chemistry 2018, 42, 20171–20179. doi:10.1039/c8nj03237h

Explore citations to this article at