Antinociceptive Effect of Ethowurtzine, a New Compound from the Class of Hexaazaizowurzitane

Analysis of specific pharmacological activity evaluated high antinociceptive efficacy of the first synthesized compound 10-di(ethoxyacetyl)-2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazatetracyclo[5,5,0,0 3,11 ,0 5,9 ]dodecane (ethowurtzine) in models of somatogenic pain of different genesis (thermal, v...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bulletin of experimental biology and medicine 2022-12, Vol.174 (2), p.230-235
Hauptverfasser: Krylova, S. G., Kiseleva, E. A., Povet’eva, T. N., Nesterova, Yu. V., Rybalkina, O. Yu, Kul’pin, P. V., Afanas’eva, O. G., Kulagina, D. A., Eremina, V. V., Baibakova, O. V., Zueva, E. P., Suslov, N. I., Sysolyatin, S. V., Zhdanov, V. V.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 235
container_issue 2
container_start_page 230
container_title Bulletin of experimental biology and medicine
container_volume 174
creator Krylova, S. G.
Kiseleva, E. A.
Povet’eva, T. N.
Nesterova, Yu. V.
Rybalkina, O. Yu
Kul’pin, P. V.
Afanas’eva, O. G.
Kulagina, D. A.
Eremina, V. V.
Baibakova, O. V.
Zueva, E. P.
Suslov, N. I.
Sysolyatin, S. V.
Zhdanov, V. V.
description Analysis of specific pharmacological activity evaluated high antinociceptive efficacy of the first synthesized compound 10-di(ethoxyacetyl)-2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazatetracyclo[5,5,0,0 3,11 ,0 5,9 ]dodecane (ethowurtzine) in models of somatogenic pain of different genesis (thermal, visceral pain, mechanical compression of paw).The new molecule from the class of hexaazaisowurtzitane effectively blocks nociceptive reactions at the supraspinal and peripheral levels of pain sensitivity organization. The effect of ethowurtzine was comparable or exceeded the effect of tramadol. The obtained results prove the possibility of creating new pharmacologically active molecules based on the high-energy substance hexaazaisowurtzitane.
doi_str_mv 10.1007/s10517-023-05679-4
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2760819685</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A746237702</galeid><sourcerecordid>A746237702</sourcerecordid><originalsourceid>FETCH-LOGICAL-c473t-3f85c980f3246a6420405685fd7f17275b8833698f01430454fa63d15ae81eb83</originalsourceid><addsrcrecordid>eNp9kV1rFDEYhYModl39A17IgCBeODWZfM7lsmytUPRG74SQnXnTTZlJ1iRjdX99M261VkRyEZI853DeHISeE3xKMJZvE8GcyBo3tMZcyLZmD9CCcElr1TTkIVrgQtVMKXWCnqR0NR-xII_RCRW8VUKwBfqy8tn50LkO9tl9g2pjLXS5Crba5F24nmI-OA9vKlN9gOtqHcZ9mHxf2RjGKu-gWg8mpRk_h-_GHIw7zKKDy8bDU_TImiHBs9t9iT6fbT6tz-uLj-_er1cXdcckzTW1inetwpY2TBjBGszKPIrbXloiG8m3SlEqWmUxYRQzzqwRtCfcgCKwVXSJXh999zF8nSBlPbrUwTCUDGFKupECK9IWy4K-_Au9ClP0Jd1MUSIIZeyOujQDaOdtyNF0s6leSSYaKmX59SU6_QdVVg-j64IH68r9PcGrPwQ7MEPepTBM2QWf7oPNEexiSCmC1fvoRhN_aIL13L0-dq8Lq392r-fQL25Hm7Yj9L8lv8ouAD0CqTz5S4h3s__H9gaYa7V4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2763161344</pqid></control><display><type>article</type><title>Antinociceptive Effect of Ethowurtzine, a New Compound from the Class of Hexaazaizowurzitane</title><source>MEDLINE</source><source>2022 ECC(Springer)</source><creator>Krylova, S. G. ; Kiseleva, E. A. ; Povet’eva, T. N. ; Nesterova, Yu. V. ; Rybalkina, O. Yu ; Kul’pin, P. V. ; Afanas’eva, O. G. ; Kulagina, D. A. ; Eremina, V. V. ; Baibakova, O. V. ; Zueva, E. P. ; Suslov, N. I. ; Sysolyatin, S. V. ; Zhdanov, V. V.</creator><creatorcontrib>Krylova, S. G. ; Kiseleva, E. A. ; Povet’eva, T. N. ; Nesterova, Yu. V. ; Rybalkina, O. Yu ; Kul’pin, P. V. ; Afanas’eva, O. G. ; Kulagina, D. A. ; Eremina, V. V. ; Baibakova, O. V. ; Zueva, E. P. ; Suslov, N. I. ; Sysolyatin, S. V. ; Zhdanov, V. V.</creatorcontrib><description>Analysis of specific pharmacological activity evaluated high antinociceptive efficacy of the first synthesized compound 10-di(ethoxyacetyl)-2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazatetracyclo[5,5,0,0 3,11 ,0 5,9 ]dodecane (ethowurtzine) in models of somatogenic pain of different genesis (thermal, visceral pain, mechanical compression of paw).The new molecule from the class of hexaazaisowurtzitane effectively blocks nociceptive reactions at the supraspinal and peripheral levels of pain sensitivity organization. The effect of ethowurtzine was comparable or exceeded the effect of tramadol. The obtained results prove the possibility of creating new pharmacologically active molecules based on the high-energy substance hexaazaisowurtzitane.</description><identifier>ISSN: 0007-4888</identifier><identifier>EISSN: 1573-8221</identifier><identifier>DOI: 10.1007/s10517-023-05679-4</identifier><identifier>PMID: 36598664</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Analgesics ; Analgesics - pharmacology ; Analgesics - therapeutic use ; Analgesics, Opioid - pharmacology ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Chemical synthesis ; Compression ; Dodecane ; Drug dosages ; Humans ; Internal Medicine ; Laboratory Medicine ; Medical research ; Opioids ; Pain ; Pain - drug therapy ; Pain Measurement - methods ; Pain perception ; Pain Threshold ; Pathology ; Pharmacology ; Regenerative medicine ; Research centers ; Tramadol ; Tramadol - pharmacology ; Tramadol - therapeutic use</subject><ispartof>Bulletin of experimental biology and medicine, 2022-12, Vol.174 (2), p.230-235</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>COPYRIGHT 2022 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-3f85c980f3246a6420405685fd7f17275b8833698f01430454fa63d15ae81eb83</citedby><cites>FETCH-LOGICAL-c473t-3f85c980f3246a6420405685fd7f17275b8833698f01430454fa63d15ae81eb83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10517-023-05679-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10517-023-05679-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36598664$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krylova, S. G.</creatorcontrib><creatorcontrib>Kiseleva, E. A.</creatorcontrib><creatorcontrib>Povet’eva, T. N.</creatorcontrib><creatorcontrib>Nesterova, Yu. V.</creatorcontrib><creatorcontrib>Rybalkina, O. Yu</creatorcontrib><creatorcontrib>Kul’pin, P. V.</creatorcontrib><creatorcontrib>Afanas’eva, O. G.</creatorcontrib><creatorcontrib>Kulagina, D. A.</creatorcontrib><creatorcontrib>Eremina, V. V.</creatorcontrib><creatorcontrib>Baibakova, O. V.</creatorcontrib><creatorcontrib>Zueva, E. P.</creatorcontrib><creatorcontrib>Suslov, N. I.</creatorcontrib><creatorcontrib>Sysolyatin, S. V.</creatorcontrib><creatorcontrib>Zhdanov, V. V.</creatorcontrib><title>Antinociceptive Effect of Ethowurtzine, a New Compound from the Class of Hexaazaizowurzitane</title><title>Bulletin of experimental biology and medicine</title><addtitle>Bull Exp Biol Med</addtitle><addtitle>Bull Exp Biol Med</addtitle><description>Analysis of specific pharmacological activity evaluated high antinociceptive efficacy of the first synthesized compound 10-di(ethoxyacetyl)-2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazatetracyclo[5,5,0,0 3,11 ,0 5,9 ]dodecane (ethowurtzine) in models of somatogenic pain of different genesis (thermal, visceral pain, mechanical compression of paw).The new molecule from the class of hexaazaisowurtzitane effectively blocks nociceptive reactions at the supraspinal and peripheral levels of pain sensitivity organization. The effect of ethowurtzine was comparable or exceeded the effect of tramadol. The obtained results prove the possibility of creating new pharmacologically active molecules based on the high-energy substance hexaazaisowurtzitane.</description><subject>Analgesics</subject><subject>Analgesics - pharmacology</subject><subject>Analgesics - therapeutic use</subject><subject>Analgesics, Opioid - pharmacology</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Chemical synthesis</subject><subject>Compression</subject><subject>Dodecane</subject><subject>Drug dosages</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Laboratory Medicine</subject><subject>Medical research</subject><subject>Opioids</subject><subject>Pain</subject><subject>Pain - drug therapy</subject><subject>Pain Measurement - methods</subject><subject>Pain perception</subject><subject>Pain Threshold</subject><subject>Pathology</subject><subject>Pharmacology</subject><subject>Regenerative medicine</subject><subject>Research centers</subject><subject>Tramadol</subject><subject>Tramadol - pharmacology</subject><subject>Tramadol - therapeutic use</subject><issn>0007-4888</issn><issn>1573-8221</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kV1rFDEYhYModl39A17IgCBeODWZfM7lsmytUPRG74SQnXnTTZlJ1iRjdX99M261VkRyEZI853DeHISeE3xKMJZvE8GcyBo3tMZcyLZmD9CCcElr1TTkIVrgQtVMKXWCnqR0NR-xII_RCRW8VUKwBfqy8tn50LkO9tl9g2pjLXS5Crba5F24nmI-OA9vKlN9gOtqHcZ9mHxf2RjGKu-gWg8mpRk_h-_GHIw7zKKDy8bDU_TImiHBs9t9iT6fbT6tz-uLj-_er1cXdcckzTW1inetwpY2TBjBGszKPIrbXloiG8m3SlEqWmUxYRQzzqwRtCfcgCKwVXSJXh999zF8nSBlPbrUwTCUDGFKupECK9IWy4K-_Au9ClP0Jd1MUSIIZeyOujQDaOdtyNF0s6leSSYaKmX59SU6_QdVVg-j64IH68r9PcGrPwQ7MEPepTBM2QWf7oPNEexiSCmC1fvoRhN_aIL13L0-dq8Lq392r-fQL25Hm7Yj9L8lv8ouAD0CqTz5S4h3s__H9gaYa7V4</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Krylova, S. G.</creator><creator>Kiseleva, E. A.</creator><creator>Povet’eva, T. N.</creator><creator>Nesterova, Yu. V.</creator><creator>Rybalkina, O. Yu</creator><creator>Kul’pin, P. V.</creator><creator>Afanas’eva, O. G.</creator><creator>Kulagina, D. A.</creator><creator>Eremina, V. V.</creator><creator>Baibakova, O. V.</creator><creator>Zueva, E. P.</creator><creator>Suslov, N. I.</creator><creator>Sysolyatin, S. V.</creator><creator>Zhdanov, V. V.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20221201</creationdate><title>Antinociceptive Effect of Ethowurtzine, a New Compound from the Class of Hexaazaizowurzitane</title><author>Krylova, S. G. ; Kiseleva, E. A. ; Povet’eva, T. N. ; Nesterova, Yu. V. ; Rybalkina, O. Yu ; Kul’pin, P. V. ; Afanas’eva, O. G. ; Kulagina, D. A. ; Eremina, V. V. ; Baibakova, O. V. ; Zueva, E. P. ; Suslov, N. I. ; Sysolyatin, S. V. ; Zhdanov, V. V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-3f85c980f3246a6420405685fd7f17275b8833698f01430454fa63d15ae81eb83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analgesics</topic><topic>Analgesics - pharmacology</topic><topic>Analgesics - therapeutic use</topic><topic>Analgesics, Opioid - pharmacology</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Chemical synthesis</topic><topic>Compression</topic><topic>Dodecane</topic><topic>Drug dosages</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Laboratory Medicine</topic><topic>Medical research</topic><topic>Opioids</topic><topic>Pain</topic><topic>Pain - drug therapy</topic><topic>Pain Measurement - methods</topic><topic>Pain perception</topic><topic>Pain Threshold</topic><topic>Pathology</topic><topic>Pharmacology</topic><topic>Regenerative medicine</topic><topic>Research centers</topic><topic>Tramadol</topic><topic>Tramadol - pharmacology</topic><topic>Tramadol - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krylova, S. G.</creatorcontrib><creatorcontrib>Kiseleva, E. A.</creatorcontrib><creatorcontrib>Povet’eva, T. N.</creatorcontrib><creatorcontrib>Nesterova, Yu. V.</creatorcontrib><creatorcontrib>Rybalkina, O. Yu</creatorcontrib><creatorcontrib>Kul’pin, P. V.</creatorcontrib><creatorcontrib>Afanas’eva, O. G.</creatorcontrib><creatorcontrib>Kulagina, D. A.</creatorcontrib><creatorcontrib>Eremina, V. V.</creatorcontrib><creatorcontrib>Baibakova, O. V.</creatorcontrib><creatorcontrib>Zueva, E. P.</creatorcontrib><creatorcontrib>Suslov, N. I.</creatorcontrib><creatorcontrib>Sysolyatin, S. V.</creatorcontrib><creatorcontrib>Zhdanov, V. V.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Bulletin of experimental biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krylova, S. G.</au><au>Kiseleva, E. A.</au><au>Povet’eva, T. N.</au><au>Nesterova, Yu. V.</au><au>Rybalkina, O. Yu</au><au>Kul’pin, P. V.</au><au>Afanas’eva, O. G.</au><au>Kulagina, D. A.</au><au>Eremina, V. V.</au><au>Baibakova, O. V.</au><au>Zueva, E. P.</au><au>Suslov, N. I.</au><au>Sysolyatin, S. V.</au><au>Zhdanov, V. V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antinociceptive Effect of Ethowurtzine, a New Compound from the Class of Hexaazaizowurzitane</atitle><jtitle>Bulletin of experimental biology and medicine</jtitle><stitle>Bull Exp Biol Med</stitle><addtitle>Bull Exp Biol Med</addtitle><date>2022-12-01</date><risdate>2022</risdate><volume>174</volume><issue>2</issue><spage>230</spage><epage>235</epage><pages>230-235</pages><issn>0007-4888</issn><eissn>1573-8221</eissn><abstract>Analysis of specific pharmacological activity evaluated high antinociceptive efficacy of the first synthesized compound 10-di(ethoxyacetyl)-2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazatetracyclo[5,5,0,0 3,11 ,0 5,9 ]dodecane (ethowurtzine) in models of somatogenic pain of different genesis (thermal, visceral pain, mechanical compression of paw).The new molecule from the class of hexaazaisowurtzitane effectively blocks nociceptive reactions at the supraspinal and peripheral levels of pain sensitivity organization. The effect of ethowurtzine was comparable or exceeded the effect of tramadol. The obtained results prove the possibility of creating new pharmacologically active molecules based on the high-energy substance hexaazaisowurtzitane.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>36598664</pmid><doi>10.1007/s10517-023-05679-4</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0007-4888
ispartof Bulletin of experimental biology and medicine, 2022-12, Vol.174 (2), p.230-235
issn 0007-4888
1573-8221
language eng
recordid cdi_proquest_miscellaneous_2760819685
source MEDLINE; 2022 ECC(Springer)
subjects Analgesics
Analgesics - pharmacology
Analgesics - therapeutic use
Analgesics, Opioid - pharmacology
Animals
Biomedical and Life Sciences
Biomedicine
Cell Biology
Chemical synthesis
Compression
Dodecane
Drug dosages
Humans
Internal Medicine
Laboratory Medicine
Medical research
Opioids
Pain
Pain - drug therapy
Pain Measurement - methods
Pain perception
Pain Threshold
Pathology
Pharmacology
Regenerative medicine
Research centers
Tramadol
Tramadol - pharmacology
Tramadol - therapeutic use
title Antinociceptive Effect of Ethowurtzine, a New Compound from the Class of Hexaazaizowurzitane
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T18%3A55%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antinociceptive%20Effect%20of%20Ethowurtzine,%20a%20New%20Compound%20from%20the%20Class%20of%20Hexaazaizowurzitane&rft.jtitle=Bulletin%20of%20experimental%20biology%20and%20medicine&rft.au=Krylova,%20S.%20G.&rft.date=2022-12-01&rft.volume=174&rft.issue=2&rft.spage=230&rft.epage=235&rft.pages=230-235&rft.issn=0007-4888&rft.eissn=1573-8221&rft_id=info:doi/10.1007/s10517-023-05679-4&rft_dat=%3Cgale_proqu%3EA746237702%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2763161344&rft_id=info:pmid/36598664&rft_galeid=A746237702&rfr_iscdi=true