{"id":188,"date":"2014-05-02T09:09:18","date_gmt":"2014-05-02T08:09:18","guid":{"rendered":"http:\/\/imramovsky.upce.cz\/?page_id=188"},"modified":"2017-10-23T11:03:59","modified_gmt":"2017-10-23T10:03:59","slug":"publications","status":"publish","type":"page","link":"https:\/\/imramovsky.upce.cz\/?page_id=188","title":{"rendered":"Publications"},"content":{"rendered":"

Publications in scientific journals (Oct 2017)<\/p>\n

    \n
  1. Du\u0161ek, J.; Imramovsk\u00fd, A.; Pauk, K.; Jorda, R.; \u0158ezn\u00ed\u010dkov\u00e1, E.; Kry\u0161tof, V. Synthesis and Antiproliferative Activities of Novel O<\/em>-Benzyl Salicylamide Derivatives. Letters in Drug Design & Discovery<\/em>, 2017<\/strong>, 14<\/em>, 662\u2013671. [ISSN: 1570-1808 (Print), IF2016 = 1,17].<\/li>\n
  2. Monteiro, S.; Imramovsk\u00fd, A.<\/strong>; Pauk, K.; Pavl\u00edk, J. Novel synthetic approach to alfaprostol key intermediates via<\/em> Stille coupling with an alkyne. Tetrahedron Letters<\/em> 2017<\/strong>, 58<\/em>(23), 2228\u20132231. [<\/strong>ISSN: 0040-4039, IF2015<\/sub> = 2,347].<\/li>\n
  3. Jorda, R.; Du\u0161ek, J.; \u0158ezn\u00ed\u010dkov\u00e1, E.; Pauk, K.; Magar, P. P.; Imramovsk\u00fd, A.<\/strong>; Kry\u0161tof, V. Synthesis and proteasomal aktivity of novel O<\/em>-benzyl salicylamid\u016f-based inhibitors bulit from leucine and phenylalanine. European Journal of Medicinal Chemistry<\/em> 2017<\/strong>, 135<\/em>, 142\u2013158. [<\/strong>ISSN: 0223-5234, IF2015<\/sub> = 3.982].<\/li>\n
  4. Machotova, J.; Zarybnicka, L.; Ruckerova, A.; Bacovska, R.; Rychly, J.; Imramovsky, A.<\/strong> Synthesis and Application of Hexaallylamino-cyclo-triphosphazene as Flame Retardant in Latex Coatings. Polymer-plastics Technology and Engineering 2017<\/strong>, 56<\/em>(5), 563-571. [ISSN: 1525-6111, IF2015<\/sub> = 1.511]<\/li>\n
  5. P\u00e1chnikov\u00e1, G.; Uldrijan, S.; Imramovsk\u00fd, A.<\/strong>; Kry\u0161tof, V.; Slaninov\u00e1, I. Substituted 2-hydroxy-N<\/em>-(arylalkyl)benzamide sensitizes cancer cells to metabolic stress by disrupting actin cytoskeleton and inhibiting autophagic flux. Toxicology in Vitro<\/em> 2016<\/strong>, 37<\/em>, 70-78. [ISSN: 0887-2333, IF2015<\/sub> = 3.338]<\/li>\n
  6. Kushkevych, I.; Kollar, P.; Ferreira, A.N.; Palma, D.; Duarte, A.; Lopes, M.M.; Bartos, M.; Pauk, K.; Imramovsk\u00fd, A.<\/strong>; Jampilek, J. Journal of Applied Biomedicine. 2016<\/strong>, 14<\/em>(2), 125-130. [ISSN: 1214-021X, IF2015<\/sub> = 1.302].<\/li>\n
  7. Zadrazilova, I.; Pospisilova, S.; Masarikova, M.; Imramovsky, A.<\/strong>; Ferriz, J.M.; Vinsova, J.; Cizek, A.; Jampilek, J. Salicylanilide carbamates: Promising antibacterial agents with high in vitro<\/em> activity against methicillin-resistant Staphylococcus aureus<\/em> (MRSA). J. Pharm. Sci.<\/em>, 2015<\/strong>, 77<\/em>, 197-207. [ISSN 0928-0987, IF2014<\/sub> = 3.350]<\/li>\n
  8. Vor\u010d\u00e1kov\u00e1, K.; \u0160t\u011bp\u00e1nkov\u00e1, \u0160.; Imramovsk\u00fd, A.<\/strong> Benzothiazoles as Effective Inhibitors of Cholinesterases: Kinetics and Mechanism of Inhibition. Sci. Pap. Univ. Pardubice<\/em> 2015<\/strong>, 21<\/em>, 31 \u2013 43.<\/li>\n
  9. Ba\u0165ov\u00e1, J.; Imramovsk\u00fd, A.<\/strong>; Hanusek, J.* Aminolysis of ezetimibe. Pharm. Biomed. Anal.<\/em> 2015<\/strong>, 107<\/em> (1), 495\u2013500. [ISSN 0731-7085, IF2013<\/sub> = 2.829]<\/li>\n
  10. Pauk, K.<\/strong>; Zadra\u017eilov\u00e1, I.; Imramovsk\u00fd, A.<\/strong>; Vin\u0161ov\u00e1, J.; Pokorn\u00e1, M.; Masa\u0159\u00edkov\u00e1, M.; \u010c\u00ed\u017eek, A.; Jamp\u00edlek, J. New derivatives of salicylamides: Preparation and antimicrobial activity against various bacterial species. Bioorganic & Medicinal Chemistry<\/em> 2013<\/strong>, 21<\/em>(21), 6574-6581. [ISSN 0968-0896, IF2012<\/sub>= 2.903].<\/li>\n
  11. Imramovsk\u00fd, A.<\/strong>; Jorda, R.; Pauk, K.<\/strong>; \u0158ezn\u00ed\u010dkov\u00e1, E.; Du\u0161ek, J.<\/strong>; Hanusek, J.; Kry\u0161tof, V. Substituted 2-hydroxy-N<\/em>-(arylalkyl)benzamides induce apoptosis in cancer cell lines. European Journal of Medicinal Chemistry<\/em> 2013<\/strong>, 68<\/em>, 253-259. [ISSN: 0223-5234, IF2012<\/sub> = 3.499].<\/li>\n
  12. Gon\u011bc, T.; Kos, J.; Zadra\u017eilov\u00e1, I.; Pe\u0161ko, M.; Govender, R.; Kelto\u0161ov\u00e1, S.; Chambel, B.; Pereira, D.; Koll\u00e1r, P.; Imramovsk\u00fd, A.<\/strong>; O\u00b4Mahony, J.; Coffey, A.; \u010c\u00ed\u017eek, A.; Kr\u00e1\u013eov\u00e1, K.; Jamp\u00edlek, J. Antibacterial and Herbicidal Activity of Ring-Substituted 2-Hydroxynaphthalene-1-carboxanilides. Molecules<\/em> 2013<\/strong>, 18<\/em>(8), 9397-9419, http:\/\/www.mdpi.com\/1420-3049\/18\/8\/9397\/pdf<\/a>. [ISSN 1420-3049, IF2012<\/sub> = 2.428].<\/li>\n
  13. Sedl\u00e1k, M.; Bhosale, D. S.; Bene\u0161, L.; Palar\u010d\u00edk J.; Kalendov\u00e1 A.; Kr\u00e1lovec K.; Imramovsk\u00fd, A.<\/strong> Synthesis and characterization of a pH-sensitive conjugate of isoniazid with Fe3O4@SiO2 magnetic nanoparticles. Bioorganic & Medicinal Chemistry Letters<\/em> 2013<\/strong>, 23<\/em>(16), 4692\u20134695. [ISSN 0960-894X, IF2011<\/sub> = 2.338].<\/li>\n
  14. Sedl\u00e1k, M.; Pejchal, V.; Imramovsk\u00fd, A.<\/strong>; Hanusek, J. A Safe and Efficient Route For The Preparation of Nitro-, Dinitro-, and Trinitrofenyl Chloroformates. Synthetic Communications 2013<\/strong>, 43<\/em>, 2365-2369. [ISSN: 0039-7911 print=1532-2432 online, IF2011<\/sub> = 1.062].<\/li>\n
  15. Pejchal, V.; Imramovsk\u00fd, A.<\/strong> Development of optimised synthesis of 4-amino-N<\/em>-(4-carbamoylphenyl)benzamide for industrial application. Research on Chemical Intermediates<\/em> 2013<\/strong>, 39, 2237-2244. [ISSN: 1568-5675 (electronic version), ISSN: 0922-6168 (print version), IF2011<\/sub> = 0.697].<\/li>\n
  16. Imramovsk\u00fd, A.<\/strong>; Pejchal, V.; \u0160t\u011bp\u00e1nkov\u00e1, \u0160.; Vor\u010d\u00e1kov\u00e1, K.; Jamp\u00edlek, J.; Van\u010do, J.; \u0160im\u016fnek, P.; Kr\u00e1lovec, K.; Br\u016f\u010dkov\u00e1, L.; Mand\u00edkov\u00e1, J.; Trejtnar, F. Synthesis and in vitro evaluation of new derivatives of 2-substituted-6-fluorobenzo[d<\/em>]thiazoles as cholinesterase inhibitors. Bioorganic & Medicinal Chemistry<\/em> 2013<\/strong>, 21<\/em>(7), 1735-1748. [ISSN 0968-0896, IF2011<\/sub>= 2.921].<\/li>\n
  17. Imramovsk\u00fd, A.<\/strong>; Stepankova, S.; Vanco, J.; Pauk, K.<\/strong>; Monreal-Ferriz, J.; Vinsova, J.; Jampilek, J. Acetylcholinesterase-Inhibiting Activity of Salicylanilide N<\/em>-Alkylcarbamates and Their Molecular Docking. Molecules<\/em> 2012<\/strong>, 17<\/em>, 10142-10158. http:\/\/www.mdpi.com\/1420-3049\/17\/9\/10142\/pdf<\/a> . [ISSN 1420-3049, IF2011<\/sub> = 2.386].<\/li>\n
  18. Imramovsk\u00fd, A.<\/strong>; Grusov\u00e1, L.<\/strong>; Bene\u0161, L.; Pejchal, V.; Sedl\u00e1k, M. Synthesis and characterization of pH-sensitive conjugate of isoniazid \u2013 methoxypoly(ethylene glycol)-b<\/em>-poly(L-lysine). Bioorganic & Medicinal Chemistry Letters<\/em> 2012<\/strong>, 22<\/em>(18), 5952-5955. [ISSN 0960-894X, IF2011<\/sub> = 2.554].<\/li>\n
  19. Abdel-Mohsen, A. M.; Abdel-Rahman, R. M.; Hrdina, R.; Imramovsk\u00fd, A.<\/strong>; Burgert, L.; Aly, A. S. Antibacterial cotton fabrics treated with core\u2013shell nanoparticles. International Journal of Biological Macromolecules<\/em> 2012<\/strong>, 50<\/em>(5), 1245-1253. [ISSN 0141-8130, IF2010<\/sub> = 2.502].<\/li>\n
  20. Imramovsk\u00fd, A.<\/strong>; Pauk, K.<\/strong>; Pad\u011blkov\u00e1, Z.; Hanusek, J. Crystal Structure of the 5-Chloro Salicylamides: Three Different Types of the H-bonding Influenced Linear Chain Formation in the Solid State. Crystals<\/em> 201<\/strong>2<\/strong>, 2<\/em>, 349-361. http:\/\/www.mdpi.com\/2073-4352\/2\/2\/349<\/a>[ISSN 2073-4352]<\/li>\n
  21. Mollaghan, A.; Vin\u0161ov\u00e1, J.; Imramovsky, A.<\/strong>; Cotter, L.; Lucey, B.; O’Mahony, J., Costelloe, A. Antistaphylococcal activity of novel salicylanilide derivatives. Current Drug Discovery Technologies <\/em>2012<\/strong>, 9<\/em>(1), 39-47. [ISSN 1570-1638].<\/li>\n
  22. Bobal, P.; Sujan, J.; Otevrel, J.; Imramovsky, A.<\/strong>; Padelkova, Z.; Jampilek, J. Microwave-Assisted Synthesis of New Substituted Anilides of Quinaldic Acid. Molecules<\/em> 2012<\/strong>, 17<\/em>, 1292-1306.http:\/\/www.mdpi.com\/1420-3049\/17\/2\/1292\/pdf<\/a>[ISSN 1420-3049, IF2010<\/sub> = 1.988].<\/li>\n
  23. Gonec, T.; Bobal, P.; Sujan, J.; Pesko, M.; Guo, J.; Kralova, K.; Pavlacka, L.; Vesely, L.; Kreckova, E.; Kos, J.; Coffey, A.; Kollar, P.; Imramovsky, A.<\/strong>; Placek, L.; Jampilek, J. Investigating the Spectrum of Biological Activity of Substituted Quinoline-2-Carboxamides and Their Isosteres. Molecules<\/em> 2012<\/strong>, 17<\/em>, 613-644. http:\/\/www.mdpi.com\/1420-3049\/17\/1\/613\/pdf<\/a> [ISSN 1420-3049, IF2010<\/sub> = 1.988].<\/li>\n
  24. B\u00edlkov\u00e1, E.; Imramovsk\u00fd, A.<\/strong>; Sedl\u00e1k, M. Recent Advances in the Design and Synthesis of Prednisolone and Methylprednisolone Conjugates. Current Pharmaceutical Design<\/em> 2011<\/strong>, 17<\/em>, 3577-3595. [ISSN: 1381-6128, IF2010<\/sub> = 4.774].<\/li>\n
  25. Vav\u0159\u00edkov\u00e1, E.; Polanc, S.; Ko\u010devar, M.; Ko\u0161mrlj, J.; Horv\u00e1ti, K.; B\u0151sze, S.; Stola\u0159\u00edkov\u00e1, J.; Imramovsk\u00fd, A.<\/strong>; Vin\u0161ov\u00e1, J. New series of isoniazid hydrazones linked with electron-withdrawing substituents. European Journal of Medicinal Chemistry<\/em> 2011<\/strong>, 46<\/em>(12), 5902-5909. [<\/strong>ISSN: 0223-5234, IF2010<\/sub> = 3.193].<\/li>\n
  26. Pejchal, V.; Stepankova, S.; Padelkova, Z.; Imramovsky, A.<\/strong>; Jampilek, J. 1,3-Substituted Imidazolidine-2,4,5-triones: Synthesis and Inhibition of Cholinergic Enzymes. Molecules<\/em> 2011<\/strong>, 16<\/em>, 7565-7582. http:\/\/www.mdpi.com\/1420-3049\/16\/9\/7565\/pdf<\/a>. [ISSN 1420-3049, IF2010<\/sub> = 1.988].<\/li>\n
  27. Imramovsky, A.<\/strong>; Pesko, M.; Ferriz, J. M.; Kralova, K.; Vinsova, J.; Jampilek, J. Photosynthesis – Inhibiting efficiency of 4-chloro-2-(chlorophenylcarbamoyl)phenyl alkylcarbamates. Bioorg Med. Chem. Lett.<\/em> 2011<\/strong>, 21<\/em>(15), 4564\u20134567. [ISSN 0960-894X, IF2010<\/sub> = 2.661].<\/li>\n
  28. B\u00edlkov\u00e1, E.; Sedl\u00e1k, M.; Imramovsk\u00fd, A.<\/strong>; Ch\u00e1rov\u00e1, P.; Knotek, P.; Bene\u0161, L. Prednisolone-alpha-cyclodextrin-star poly(ethylene glycol) polypseudorotaxane with delayed pH-sensitivity as a targeted drug delivery system. Int. J. Pharm.<\/em>2011<\/strong>, 414<\/em>(1-2), 42-47. [ISSN 0378-5173, IF2010<\/sub>=3.607].<\/li>\n
  29. Imramovsk\u00fd, A.<\/strong>; Pauk, K.<\/strong>; Pejchal, V.; Hanusek, J. Salicylanilides and Their Derivates as Perspective Anti-tuberculosis Drugs: Synthetic Routes and Biological Evaluations. Mini-Reviews in Organic Chemistry<\/em> 2011<\/strong>, 8<\/em>, 211-220. [ISSN: 1570-193X, IF2010<\/sub>=1.448].<\/li>\n
  30. Imramovsk\u00fd, A.<\/strong>; Pe\u0161ko, M.; Kr\u00e1lov\u00e1, K.; Vejsov\u00e1, M.; Stola\u0159\u00edkov\u00e1, J.; Vin\u0161ov\u00e1, J.; Jamp\u00edlek, J. Investigating Spectrum of Biological Activity of 4- and 5-Chloro-2-hydroxy-N<\/em>-[2-(arylamino)-1-alkyl-2-oxoethyl]benzamides. Molecules<\/em> 2011<\/strong>, 16<\/em>, 2414-2430. [ISSN 1420-3049, IF2010<\/sub>=1.608].<\/li>\n
  31. Imramovsk\u00fd, A.<\/strong>; Monreal, J. F.; Pauk, K.<\/strong>; Kr\u00e1tk\u00fd, M.; Vin\u0161ov\u00e1, J. Synthetic Route for the Preparation of 2-Hydroxy-N<\/em>-[1-(2-hydroxyphenylamino)- 1-oxoalkan-2-yl]benzamides. J. Comb. Chem. <\/em>2010<\/strong>, 12<\/em>(4), <\/em>414-416. [ISSN 1520-4766, IF2009<\/sub>= 3.450]<\/li>\n
  32. Monreal, J. F.; V\u00e1vrov\u00e1, K.; Kunc, F.; Imramovsk\u00fd, A.<\/strong>; Stola\u0159\u00edkov\u00e1, J.; Vav\u0159\u00edkov\u00e1, E.; Vin\u0161ov\u00e1, J. Salicylanilide carbamates: Antitubercular agents active against multidrug-resistant Mycobacterium tuberculosis strains. Bioorg. Med. Chem.<\/em>, 2010<\/strong>, 18<\/em>(3), 1054\u20131061. [ISSN 0968-0896, IF2009<\/sub>= 2.822]<\/li>\n
  33. B\u00edlkov\u00e1, E; Imramovsk\u00fd, A.<\/strong>; Buchta, V.; Sedl\u00e1k, M. Targeted antifungal delivery system: Glucosidase sensitive nystatin\u2013star poly(ethylene glycol) conjugate. Int. J. Pharm.<\/em> 2010<\/strong>, 386<\/em>(1-2), 1-5. [ISSN 0378-5173, IF2009<\/sub>=3.061]<\/li>\n
  34. Vin\u0161ov\u00e1, J.; Imramovsk\u00fd, A.<\/strong>; Kr\u00e1tk\u00fd, M.; Monreal, J. F.; Pal\u00e1t, K.; Ly\u010dka A.; R\u016f\u017ei\u010dka, A.; An unprecedent rearrangement of salicylanilide derivates: imidazolinone intermediate formation. Tetrahedron Lett.<\/em> 2010<\/strong>, 51<\/em>(1), 23-26. [ISSN 0040-4039, IF2009<\/sub>= 2.539]<\/li>\n
  35. Imramovsk\u00fd, A.<\/strong>; Vin\u0161ov\u00e1, J.;Monreal, J. F.; Dole\u017eal, R.; Jamp\u00edlek, J.; Kaustov\u00e1, J.; Kunc, F. New Antituberculotics Originated from Salicylanilides with Promising In Vitro<\/em> Activity against Atypical Mycobacterial Strains. Bioorg. Med. Chem.<\/em>, 2009<\/strong>, 17<\/em>(10), 3572-3579. [ISSN 0968-0896, IF2007<\/sub>= 2.662]<\/li>\n
  36. Imramovsk\u00fd, A.<\/strong>; Vin\u0161ov\u00e1, J.;Monreal, J. F.; Buchta, V.; Jamp\u00edlek, J. Salicylanilide esters of N<\/em>-protected amino acids as novel antimicrobial agents. Bioorg. Med. Chem. Lett. <\/em>2009<\/strong>, 19<\/em>(2), 348-351. [ISSN 0960-894X, IF2007<\/sub> = 2.604]<\/li>\n
  37. Jampilek, J.; Reckova, Z.; Imramovsky, A.<\/strong>; Raich, I.; Vinsova, J.; Dohnal, J. Stability Study of New Effective Antimycobacterial Mutual Prodrugs. Curr. Org. Chem.<\/em> 2008<\/strong>, 12<\/em>(8), 667-674.[ISSN 1385-2728, IF2006<\/sub> = 3.961]<\/li>\n
  38. Vin\u0161ov\u00e1, J.; Imramovsk\u00fd, A.<\/strong>; Jamp\u00edlek, J.; Monreal, J. F.; Dole\u017eal M. Recent Advances on Isoniazide Derivatives. Anti-Infective agents Med. Chem.<\/em>2008<\/strong>, 7<\/em>(1), 1-20. [ISSN 1871-5214]<\/li>\n
  39. Imramovsk\u00fd, A.<\/strong>; Polanc, S.; Vin\u0161ov\u00e1, J.; Ko\u010devar, M.; Jamp\u00edlek, J.; Re\u010dkov\u00e1, Z.; Kaustov\u00e1, J. A new modification of anti-tubercular active molecules. Bioorg. Med. Chem.<\/em> 2007<\/strong>, 15<\/em>(7), 2551-2559. [ISSN 0968-0896, IF2006<\/sub>= 2.624]<\/li>\n
  40. Vin\u0161ov\u00e1, J.; Imramovsk\u00fd, A.<\/strong>; Buchta, V.; \u010ce\u010dkov\u00e1, M; Dole\u017eal, M; \u0160taud, F.; Jamp\u00edlek, J.; Kaustov\u00e1, J. Salicylanilide acetates: Synthesis and Antibacterial Evaluation. Molecules<\/em>, 2007<\/strong>, 12<\/em>, 1-12. [ISSN 1420-3049, IF2006<\/sub>= 0.841]<\/li>\n
  41. Imramovsk\u00fd, A.<\/strong>; Vin\u0161ov\u00e1, J.; Monreal F\u00e9rriz, J.; Kune\u0161, J.; Pour, M.; Dole\u017eal, M. Salicylanilide esterification: unexpected formation of novel 7-membered rings. Tetrahedron Lett.<\/em>, 2006<\/strong>, 47<\/em>(29), 5007-5011. [ISSN 0040-4039, IF2005<\/sub>= 2.477]<\/li>\n
  42. Vin\u0161ov\u00e1, J.; Imramovsk\u00fd, A.<\/strong> Intramolekul\u00e1rn\u00ed cyklizace vyu\u017e\u00edvan\u00e9 k uvol\u0148ov\u00e1n\u00ed \u00fa\u010dinn\u00fdch l\u00e1tek z prol\u00e9\u010div. Chem. Listy<\/em>, 2005<\/strong>, 99<\/em>(1), 21-29. [ISSN 0009-2770, IF2006<\/sub>= 0.445]<\/li>\n
  43. Vin\u0161ov\u00e1, J.; Imramovsk\u00fd, A.<\/strong> Salicylanilidy \u2013 st\u00e1le aktu\u00e1ln\u00ed skupina s potenci\u00e1ln\u00ed antibakteri\u00e1ln\u00ed aktivitou. Ces. Slov. Farm.<\/em> 2004<\/strong>, 53,<\/em> 294-299. [ISSN 1210-7816].<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    Publications in scientific journals (Oct 2017) Du\u0161ek, J.; Imramovsk\u00fd, A.; Pauk, K.; Jorda, R.; \u0158ezn\u00ed\u010dkov\u00e1, E.; Kry\u0161tof, V. Synthesis and Antiproliferative Activities of Novel O-Benzyl Salicylamide Derivatives. Letters in Drug Design & Discovery, 2017, 14, 662\u2013671. [ISSN: 1570-1808 (Print), IF2016 = 1,17]. Monteiro, S.; Imramovsk\u00fd, A.; Pauk, K.; Pavl\u00edk, J. \u2026 Continue reading → <\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":5,"comment_status":"closed","ping_status":"closed","template":"","meta":{"ngg_post_thumbnail":0,"footnotes":""},"class_list":["post-188","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=\/wp\/v2\/pages\/188","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=188"}],"version-history":[{"count":10,"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=\/wp\/v2\/pages\/188\/revisions"}],"predecessor-version":[{"id":1004,"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=\/wp\/v2\/pages\/188\/revisions\/1004"}],"wp:attachment":[{"href":"https:\/\/imramovsky.upce.cz\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=188"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}