Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1994, 59, 234-238
https://doi.org/10.1135/cccc19940234

New Groups of Potential Antituberculotics: Bis(1-aryltetrazol-5-yl) Disulfides. Structure Activity Relationship

Karel Waissera, Jiří Kuneša, Alexandr Hrabáleka and Želmíra Odlerováb

a Department of Inorganic and Organic Chemistry, Faculty of Pharmacy, Charles University, 501 65 Hradec Králové, Czech Republic
b Institute of Preventive and Clinical Medicine, 803 01 Bratislava, Slovak Republic

Crossref Cited-by Linking

  • Myznikov L. V., Vorona S. V., Artamonova T. V., Zevatskii Yu. E.: Tetrazoles with oxygen-, sulfur-, and selenium-containing substituents. Russ Chem Bull 2016, 65, 923. <https://doi.org/10.1007/s11172-016-1394-z>
  • Li Xiong, Liu Linfeng, Liu Guanghui, Rong Yaoguang, Yang Ying, Wang Heng, Ku Zhiliang, Xu Mi, Zhong Cheng, Han Hongwei: Efficient Dye‐Sensitized Solar Cells with Potential‐Tunable Organic Sulfide Mediators and Graphene‐Modified Carbon Counter Electrodes. Adv Funct Materials 2013, 23, 3344. <https://doi.org/10.1002/adfm.201203374>
  • Efimova Yu.A., Artamonova T.V., Hrabalek A., Koldobskii G. I.: Microwave-assisted oxidation of 1-substituted tetrazole-5-thiones. Russ J Org Chem 2010, 46, 153. <https://doi.org/10.1134/S1070428010010185>
  • Myznikov L. V., Hrabalek A., Koldobskii G. I.: Drugs in the tetrazole series. (Review). Chem Heterocycl Compd 2007, 43, 1. <https://doi.org/10.1007/s10593-007-0001-5>
  • Kubicová Lenka, Šustr Martin, Kráľová Katarína, Chobot Vladimír, Vytlačilová Jitka, Jahodář Luděk, Vuorela Pia, Macháček Miloš, Kaustová Jarmila: Synthesis and Biological Evaluation of Quinazoline-4-thiones. Molecules 2003, 8, 756. <https://doi.org/10.3390/81100756>
  • Kayukova L. A., Praliev K. D.: Main directions in the search for new antituberculous drugs (review). Pharm Chem J 2000, 34, 11. <https://doi.org/10.1007/BF02524551>