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Collect. Czech. Chem. Commun. 2008, 73, 627-636
https://doi.org/10.1135/cccc20080627

Synthesis and Biological Evaluation of Some A,D-Ring Modified 16,17-Secoandrostane Derivatives

Evgenija A. Djurendića, Marina P. Zaviša, Marija N. Sakača,*, Vesna V. Kojićb, Gordana M. Bogdanovićb and Katarina M. Penov Gašia

a Department of Chemistry, Faculty of Sciences, University of Novi Sad, 21000 Novi Sad, Trg Dositeja Obradovića 3, Serbia
b Oncology Institute of Vojvodina, Institutski put 4, 21204 Sremska Kamenica, Serbia

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  • Ilovaisky Alexey I., Scherbakov Alexander M., Chernoburova Elena I., Shchetinina Marina A., Merkulova Valentina M., Bogdanov Fedor B., Sorokin Danila V., Salnikova Diana I., Bozhenko Eugene I., Zavarzin Igor V., Terent’ev Alexander O.: Secosteroid diacylhydrazines as novel effective agents against hormone-dependent breast cancer cells. The Journal of Steroid Biochemistry and Molecular Biology 2024, 244, 106597. <https://doi.org/10.1016/j.jsbmb.2024.106597>
  • Šestić Tijana Lj., Ajduković Jovana J., Marinović Maja A., Petri Edward T., Savić Marina P.: In silico ADMET analysis of the A-, B- and D-modified androstane derivatives with potential anticancer effects. Steroids 2023, 189, 109147. <https://doi.org/10.1016/j.steroids.2022.109147>
  • Dzichenka Yaraslau, Shapira Michail, Yantsevich Aliaksei, Cherkesova Tatsiana, Grbović Ljubica, Savić Marina, Usanov Sergey, Jovanović-Šanta Suzana: Modified bile acids and androstanes—Novel promising inhibitors of human cytochrome P450 17A1. The Journal of Steroid Biochemistry and Molecular Biology 2021, 205, 105777. <https://doi.org/10.1016/j.jsbmb.2020.105777>
  • Kovačević Strahinja Z., Podunavac-Kuzmanović Sanja O., Jevrić Lidija R., Vukić Vladimir R., Savić Marina P., Djurendić Evgenija A.: Preselection of A- and B- modified d-homo lactone and d-seco androstane derivatives as potent compounds with antiproliferative activity against breast and prostate cancer cells – QSAR approach and molecular docking analysis. European Journal of Pharmaceutical Sciences 2016, 93, 107. <https://doi.org/10.1016/j.ejps.2016.08.009>
  • Gaši Katarina, Djurendić Evgenija, Dojčinović-Vujašković Sanja, Gaković Andrea, Jovanović-Šanta Suzana, Kojić Vesna, Sakač Marija: Synthesis, anti-oxidant activity, and cytotoxicity of salicyloyl derivatives of estra-1,3,5(10)-triene and androst-5-ene. Chemical Papers 2012, 66. <https://doi.org/10.2478/s11696-012-0150-6>
  • Hanson James R.: Steroids: partial synthesis in medicinal chemistry. Nat. Prod. Rep. 2010, 27, 887. <https://doi.org/10.1039/c001262a>
  • Djurendic Evgenija A., Zavis Marina P., Sakac Marija N., Kojic Vesna V., Bogdanovic Gordana M., Penov Gasi Katarina M.: ChemInform Abstract: Synthesis and Biological Evaluation of Some A,D‐Ring Modified 16,17‐Secoandrostane Derivatives. ChemInform 2009, 40. <https://doi.org/10.1002/chin.200901201>
  • Djurendić Evgenija A., Zaviš Marina P., Sakač Marija N., Čanadi Janoš J., Kojić Vesna V., Bogdanović Gordana M., Penov Gaši Katarina M.: Synthesis and antitumor activity of new d-seco and d-homo androstane derivatives. Steroid 2009, 74, 983. <https://doi.org/10.1016/j.steroids.2009.07.007>