Mendeleev Communications
RUS  ENG    JOURNALS   PEOPLE   ORGANISATIONS   CONFERENCES   SEMINARS   VIDEO LIBRARY   PACKAGE AMSBIB  
General information
Latest issue
Archive

Search papers
Search references

RSS
Latest issue
Current issues
Archive issues
What is RSS



Mendeleev Commun.:
Year:
Volume:
Issue:
Page:
Find






Personal entry:
Login:
Password:
Save password
Enter
Forgotten password?
Register


Mendeleev Communications, 2017, Volume 27, Issue 5, Pages 439–442
DOI: https://doi.org/10.1016/j.mencom.2017.09.002
(Mi mendc2019)
 

This article is cited in 20 scientific papers (total in 20 papers)

Communications

Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis

D. O. Primaab, E. V. Vorontsovac, A. G. Makarova, A. Yu. Makarova, I. Yu. Bagryanskayaad, T. F. Mikhailovskayaa, Yu. G. Slizhovb, A. V. Zibarevab

a N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
b Department of Chemistry, National Research Tomsk State University, Tomsk, Russian Federation
c Institute of Molecular Biology and Biophysics, Federal Research Center of Fundamental and Translational Medicine, Novosibirsk, Russian Federation
d Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
Abstract: The title compounds synthesized from halogenated arene-1,2-diamines revealed, together with the latter, cytotoxicity towards the Hep2 (laryngeal epidermoid carcinoma) cells. The cytotoxicity was high and was accompanied by pronounced apoptotic activity at low concentrations for fluorinated diazoles, triazoles and selenadiazoles.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (795.4 Kb)


Citation: D. O. Prima, E. V. Vorontsova, A. G. Makarov, A. Yu. Makarov, I. Yu. Bagryanskaya, T. F. Mikhailovskaya, Yu. G. Slizhov, A. V. Zibarev, “Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis”, Mendeleev Commun., 27:5 (2017), 439–442
Linking options:
  • https://www.mathnet.ru/eng/mendc2019
  • https://www.mathnet.ru/eng/mendc/v27/i5/p439
  • This publication is cited in the following 20 articles:
    1. Tristan Georges, Jacynthe Beaudoin, Mubassira Rahman, Alireza Nari, Jeffrey S. Ovens, David L. Bryce, “77Se Solid-State NMR Investigation of Selenium Chemical Shift Tensors of Chalcogen Bonds in Selenadiazole Cocrystals”, J. Phys. Chem. C, 2025  crossref
    2. Oleg A. Rakitin, Advances in Heterocyclic Chemistry, 142, 2024, 227  crossref
    3. Iwona Zarzyka, Anna Czerniecka-Kubicka, Agnieszka Szyszkowska, Michał Longosz, Lucjan Dobrowolski, Weronika Gonciarz, Magdalena Chmiela, Damian Trzybiński, Agata Wróbel, Krzysztof Woźniak, Karol Hȩclik, “Molecular modeling of 3‑chloro-3-phenylquinoline-2,4‑dione, crystal structure and cytotoxic activity for developments in a potential new drug”, Journal of Molecular Structure, 1284 (2023), 135353  crossref
    4. Elena A. Chulanova, Ekaterina A. Radiush, Nikolay A. Semenov, Emanuel Hupf, Irina G. Irtegova, Yulia S. Kosenkova, Irina Yu. Bagryanskaya, Leonid A. Shundrin, Jens Beckmann, Andrey V. Zibarev, “Tuning Molecular Electron Affinities against Atomic Electronegativities by Spatial Expansion of a π‐System”, ChemPhysChem, 24:9 (2023)  crossref
    5. Asmaa E. Kassab, “Benzotriazole scaffold: An overview of antiproliferative potential, mechanisms of action, and structure–activity relationships”, Archiv der Pharmazie, 356:8 (2023)  crossref
    6. V. Turukarabettu, B. Kalluraya, P. Kumar, R. B. Chandrashekarappa, S. Varija Raghu, “Nano Au/TiO2 Catalyzed Click Synthesis of Novel 1,2,3-Triazoles from S-Propargyl-1,2,4-triazole: Antibacterial Activity, Toxicity, and Docking Analysis”, Russ J Gen Chem, 93:10 (2023), 2638  crossref
    7. Guofa Ren, Kangming Wu, Jing An, Yu Shang, Kewen Zheng, Zhiqiang Yu, “Toxicity Assessment of Octachlorostyrene in Human Liver Carcinoma (HepG2) Cells”, IJERPH, 19:21 (2022), 14272  crossref
    8. Shoko Yamazaki, Comprehensive Heterocyclic Chemistry IV, 2022, 303  crossref
    9. Nidhi Jangir, Poonam, Surbhi Dhadda, Dinesh K. Jangid, “Recent advances in the synthesis of five‐ and six‐membered heterocycles as bioactive skeleton: A concise overview”, ChemistrySelect, 7:6 (2022)  crossref
    10. Oleg A. Rakitin, Comprehensive Heterocyclic Chemistry IV, 2022, 371  crossref
    11. Edward R.T. Tiekink, “Supramolecular aggregation patterns featuring Se⋯N secondary-bonding interactions in mono-nuclear selenium compounds: A comparison with their congeners”, Coordination Chemistry Reviews, 443 (2021), 214031  crossref
    12. Mariusz Michalczyk, Magdalena Malik, Wiktor Zierkiewicz, Steve Scheiner, “Experimental and Theoretical Studies of Dimers Stabilized by Two Chalcogen Bonds in the Presence of a N···N Pnicogen Bond”, J. Phys. Chem. A, 125:2 (2021), 657  crossref
    13. Elisabeth Parman, Märt Lõkov, Robert Järviste, Sofja Tshepelevitsh, Nikolay A. Semenov, Elena A. Chulanova, Georgy E. Salnikov, Darya O. Prima, Yuri G. Slizhov, Ivo Leito, Andrey V. Zibarev, “Acid‐Base and Anion Binding Properties of Tetrafluorinated 1,3‐Benzodiazole, 1,2,3‐Benzotriazole and 2,1,3‐Benzoselenadiazole”, ChemPhysChem, 22:22 (2021), 2329  crossref
    14. Oleg A. Rakitin, “Fused 1,2,5-thia- and 1,2,5-selenadiazoles: Synthesis and application in materials chemistry”, Tetrahedron Letters, 61:34 (2020), 152230  crossref
    15. G. A. Selivanova, E. V. Tretyakov, “Fluorinated benzimidazoles for medicinal chemistry and new materials”, Russ Chem Bull, 69:5 (2020), 838  crossref
    16. Elena Chugunova, Almir Gazizov, Marina Sazykina, Nurgali Akylbekov, Anastasiya Gildebrant, Ivan Sazykin, Alexander Burilov, Nurbol Appazov, Shorena Karchava, Maria Klimova, Alexandra Voloshina, Anastasia Sapunova, Syumbelya Gumerova, Ayrat Khamatgalimov, Tatiana Gerasimova, Alexey Dobrynin, Olga Gogoleva, Vladimir Gorshkov, “Design of Novel 4-Aminobenzofuroxans and Evaluation of Their Antimicrobial and Anticancer Activity”, IJMS, 21:21 (2020), 8292  crossref
    17. T. S. Sukhikh, D. S. Ogienko, D. A. Bashirov, S. N. Konchenkoa, “Luminescent complexes of 2,1,3-benzothiadiazole derivatives”, Russ Chem Bull, 68:4 (2019), 651  crossref
    18. Darya O. Prima, Arkady G. Makarov, Irina Yu. Bagryanskaya, Andrey E. Kolesnikov, Leila V. Zargarova, Dmitry S. Baev, Tatiana F. Eliseeva, Larisa V. Politanskaya, Alexander Yu. Makarov, Yuri G. Slizhov, Andrey V. Zibarev, “Fluorine‐Containing n‐6 and Angular and Linear n‐6‐n' (n, n' = 5, 6, 7) Diaza‐Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way”, ChemistrySelect, 4:8 (2019), 2383  crossref
    19. L. V. Politanskaya, G. A. Selivanova, E. V. Panteleeva, E. V. Tretyakov, V. E. Platonov, P. V. Nikul'shin, A. S. Vinogradov, Ya. V. Zonov, V. M. Karpov, T. V. Mezhenkova, A. V. Vasilyev, A. B. Koldobskii, O. S. Shilova, S. M. Morozova, Ya. V. Burgart, E. V. Shchegolkov, V. I. Saloutin, V. B. Sokolov, A. Yu. Aksinenko, V. G. Nenajdenko, M. Yu. Moskalik, V. V. Astakhova, B. A. Shainyan, A. A. Tabolin, S. L. Ioffe, V. M. Muzalevskiy, E. S. Balenkova, A. V. Shastin, A. A. Tyutyunov, V. E. Boiko, S. M. Igumnov, A. D. Dilman, N. Yu. Adonin, V. V. Bardin, S. M. Masoud, D. V. Vorobyeva, S. N. Osipov, E. V. Nosova, G. N. Lipunova, V. N. Charushin, D. O. Prima, A. G. Makarov, A. V. Zibarev, B. A. Trofimov, L. N. Sobenina, K. V. Belyaeva, V. Ya. Sosnovskikh, D. L. Obydennov, S. A. Usachev, “Organofluorine chemistry: promising growth areas and challenges”, Russian Chem. Reviews, 88:5 (2019), 425–569  mathnet  mathnet  crossref  isi  scopus
    20. Oleg A. Rakitin, Andrey V. Zibarev, “Synthesis and Applications of 5‐Membered Chalcogen‐Nitrogen π‐Heterocycles with Three Heteroatoms”, Asian J Org Chem, 7:12 (2018), 2397  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
    Mendeleev Communications
    Statistics & downloads:
    Abstract page:31
    Full-text PDF :6
     
      Contact us:
     Terms of Use  Registration to the website  Logotypes © Steklov Mathematical Institute RAS, 2025