Novel Acylhydrazones Based on 1-Decylisatins and Girard Reagent T Possessing Antimicrobial Activity
By the reaction of new 1-decyl substituted isatin derivatives with Girard reagent T novel ammonium salts were obtained. These compounds display a moderate antimicrobial activity against gram-positive Staphylococcus aureus and Bacillus cereus bacterial strains with low hemotoxicity. Study of the infl...
Gespeichert in:
Veröffentlicht in: | Russian journal of general chemistry 2024-11, Vol.94 (11), p.3099-3103 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3103 |
---|---|
container_issue | 11 |
container_start_page | 3099 |
container_title | Russian journal of general chemistry |
container_volume | 94 |
creator | Bogdanov, A. V. Voloshina, A. D. Il’in, A. V. Kadomtseva, M. E. Pashirova, T. N. Shaihutdinova, Z. M. Mironov, V. F. |
description | By the reaction of new 1-decyl substituted isatin derivatives with Girard reagent T novel ammonium salts were obtained. These compounds display a moderate antimicrobial activity against gram-positive
Staphylococcus aureus
and
Bacillus cereus
bacterial strains with low hemotoxicity. Study of the influence of the structure of substituents in the heterocycle aromatic fragment on the self-assembly process and antimicrobial activity may indirectly indicate that the antimicrobial action of amphiphilic ammonium compounds based on the isatin scaffold is different from classical cationic surfactants. |
doi_str_mv | 10.1134/S1070363224110331 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_3146496795</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3146496795</sourcerecordid><originalsourceid>FETCH-LOGICAL-c198t-8edd116e06bbee953f62a36e6706c9b7349b15d3f6bda05fa94935baa75822e63</originalsourceid><addsrcrecordid>eNp1kEFPwzAMhSMEEmPwA7hF4lyImzZtj2OwgTQBgnGu0sYdmbZ0xN2k8uvJNCQOiJMtv_c-W2bsEsQ1gExu3kBkQioZxwmAkBKO2ACUyCMpU3Ec-iBHe_2UnREthQAhVDxg9VO7wxUf1f3qozdef7UOid9qQsNbxyG6wyBZ0p11xLUzfGq99oa_ol6g6_icv7RESGTdgo9cZ9e29m1l9R7a2Z3t-nN20ugV4cVPHbL3yf18_BDNnqeP49EsqqHIuyhHYwAUClVViEUqGxVrqVBlQtVFlcmkqCA1YVwZLdJGF0kh00rrLM3jGJUcsqsDd-Pbzy1SVy7brXdhZSkhUUmhskAdMji4wplEHpty4-1a-74EUe5_Wf75ZcjEhwwFr1ug_yX_H_oGUw11tA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3146496795</pqid></control><display><type>article</type><title>Novel Acylhydrazones Based on 1-Decylisatins and Girard Reagent T Possessing Antimicrobial Activity</title><source>SpringerLink Journals - AutoHoldings</source><creator>Bogdanov, A. V. ; Voloshina, A. D. ; Il’in, A. V. ; Kadomtseva, M. E. ; Pashirova, T. N. ; Shaihutdinova, Z. M. ; Mironov, V. F.</creator><creatorcontrib>Bogdanov, A. V. ; Voloshina, A. D. ; Il’in, A. V. ; Kadomtseva, M. E. ; Pashirova, T. N. ; Shaihutdinova, Z. M. ; Mironov, V. F.</creatorcontrib><description>By the reaction of new 1-decyl substituted isatin derivatives with Girard reagent T novel ammonium salts were obtained. These compounds display a moderate antimicrobial activity against gram-positive
Staphylococcus aureus
and
Bacillus cereus
bacterial strains with low hemotoxicity. Study of the influence of the structure of substituents in the heterocycle aromatic fragment on the self-assembly process and antimicrobial activity may indirectly indicate that the antimicrobial action of amphiphilic ammonium compounds based on the isatin scaffold is different from classical cationic surfactants.</description><identifier>ISSN: 1070-3632</identifier><identifier>EISSN: 1608-3350</identifier><identifier>DOI: 10.1134/S1070363224110331</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Ammonium compounds ; Aromatic compounds ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Reagents ; Self-assembly</subject><ispartof>Russian journal of general chemistry, 2024-11, Vol.94 (11), p.3099-3103</ispartof><rights>Pleiades Publishing, Ltd. 2024</rights><rights>Copyright Springer Nature B.V. 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c198t-8edd116e06bbee953f62a36e6706c9b7349b15d3f6bda05fa94935baa75822e63</cites><orcidid>0009-0008-5713-4137 ; 0000-0002-9547-5564 ; 0000-0002-4198-3774 ; 0000-0002-2706-9898 ; 0000-0002-3540-8554 ; 0000-0002-2483-4742 ; 0000-0002-2001-1570</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1070363224110331$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1070363224110331$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Bogdanov, A. V.</creatorcontrib><creatorcontrib>Voloshina, A. D.</creatorcontrib><creatorcontrib>Il’in, A. V.</creatorcontrib><creatorcontrib>Kadomtseva, M. E.</creatorcontrib><creatorcontrib>Pashirova, T. N.</creatorcontrib><creatorcontrib>Shaihutdinova, Z. M.</creatorcontrib><creatorcontrib>Mironov, V. F.</creatorcontrib><title>Novel Acylhydrazones Based on 1-Decylisatins and Girard Reagent T Possessing Antimicrobial Activity</title><title>Russian journal of general chemistry</title><addtitle>Russ J Gen Chem</addtitle><description>By the reaction of new 1-decyl substituted isatin derivatives with Girard reagent T novel ammonium salts were obtained. These compounds display a moderate antimicrobial activity against gram-positive
Staphylococcus aureus
and
Bacillus cereus
bacterial strains with low hemotoxicity. Study of the influence of the structure of substituents in the heterocycle aromatic fragment on the self-assembly process and antimicrobial activity may indirectly indicate that the antimicrobial action of amphiphilic ammonium compounds based on the isatin scaffold is different from classical cationic surfactants.</description><subject>Ammonium compounds</subject><subject>Aromatic compounds</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Reagents</subject><subject>Self-assembly</subject><issn>1070-3632</issn><issn>1608-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kEFPwzAMhSMEEmPwA7hF4lyImzZtj2OwgTQBgnGu0sYdmbZ0xN2k8uvJNCQOiJMtv_c-W2bsEsQ1gExu3kBkQioZxwmAkBKO2ACUyCMpU3Ec-iBHe_2UnREthQAhVDxg9VO7wxUf1f3qozdef7UOid9qQsNbxyG6wyBZ0p11xLUzfGq99oa_ol6g6_icv7RESGTdgo9cZ9e29m1l9R7a2Z3t-nN20ugV4cVPHbL3yf18_BDNnqeP49EsqqHIuyhHYwAUClVViEUqGxVrqVBlQtVFlcmkqCA1YVwZLdJGF0kh00rrLM3jGJUcsqsDd-Pbzy1SVy7brXdhZSkhUUmhskAdMji4wplEHpty4-1a-74EUe5_Wf75ZcjEhwwFr1ug_yX_H_oGUw11tA</recordid><startdate>20241101</startdate><enddate>20241101</enddate><creator>Bogdanov, A. V.</creator><creator>Voloshina, A. D.</creator><creator>Il’in, A. V.</creator><creator>Kadomtseva, M. E.</creator><creator>Pashirova, T. N.</creator><creator>Shaihutdinova, Z. M.</creator><creator>Mironov, V. F.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0009-0008-5713-4137</orcidid><orcidid>https://orcid.org/0000-0002-9547-5564</orcidid><orcidid>https://orcid.org/0000-0002-4198-3774</orcidid><orcidid>https://orcid.org/0000-0002-2706-9898</orcidid><orcidid>https://orcid.org/0000-0002-3540-8554</orcidid><orcidid>https://orcid.org/0000-0002-2483-4742</orcidid><orcidid>https://orcid.org/0000-0002-2001-1570</orcidid></search><sort><creationdate>20241101</creationdate><title>Novel Acylhydrazones Based on 1-Decylisatins and Girard Reagent T Possessing Antimicrobial Activity</title><author>Bogdanov, A. V. ; Voloshina, A. D. ; Il’in, A. V. ; Kadomtseva, M. E. ; Pashirova, T. N. ; Shaihutdinova, Z. M. ; Mironov, V. F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c198t-8edd116e06bbee953f62a36e6706c9b7349b15d3f6bda05fa94935baa75822e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Ammonium compounds</topic><topic>Aromatic compounds</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Reagents</topic><topic>Self-assembly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bogdanov, A. V.</creatorcontrib><creatorcontrib>Voloshina, A. D.</creatorcontrib><creatorcontrib>Il’in, A. V.</creatorcontrib><creatorcontrib>Kadomtseva, M. E.</creatorcontrib><creatorcontrib>Pashirova, T. N.</creatorcontrib><creatorcontrib>Shaihutdinova, Z. M.</creatorcontrib><creatorcontrib>Mironov, V. F.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of general chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bogdanov, A. V.</au><au>Voloshina, A. D.</au><au>Il’in, A. V.</au><au>Kadomtseva, M. E.</au><au>Pashirova, T. N.</au><au>Shaihutdinova, Z. M.</au><au>Mironov, V. F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel Acylhydrazones Based on 1-Decylisatins and Girard Reagent T Possessing Antimicrobial Activity</atitle><jtitle>Russian journal of general chemistry</jtitle><stitle>Russ J Gen Chem</stitle><date>2024-11-01</date><risdate>2024</risdate><volume>94</volume><issue>11</issue><spage>3099</spage><epage>3103</epage><pages>3099-3103</pages><issn>1070-3632</issn><eissn>1608-3350</eissn><abstract>By the reaction of new 1-decyl substituted isatin derivatives with Girard reagent T novel ammonium salts were obtained. These compounds display a moderate antimicrobial activity against gram-positive
Staphylococcus aureus
and
Bacillus cereus
bacterial strains with low hemotoxicity. Study of the influence of the structure of substituents in the heterocycle aromatic fragment on the self-assembly process and antimicrobial activity may indirectly indicate that the antimicrobial action of amphiphilic ammonium compounds based on the isatin scaffold is different from classical cationic surfactants.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1070363224110331</doi><tpages>5</tpages><orcidid>https://orcid.org/0009-0008-5713-4137</orcidid><orcidid>https://orcid.org/0000-0002-9547-5564</orcidid><orcidid>https://orcid.org/0000-0002-4198-3774</orcidid><orcidid>https://orcid.org/0000-0002-2706-9898</orcidid><orcidid>https://orcid.org/0000-0002-3540-8554</orcidid><orcidid>https://orcid.org/0000-0002-2483-4742</orcidid><orcidid>https://orcid.org/0000-0002-2001-1570</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1070-3632 |
ispartof | Russian journal of general chemistry, 2024-11, Vol.94 (11), p.3099-3103 |
issn | 1070-3632 1608-3350 |
language | eng |
recordid | cdi_proquest_journals_3146496795 |
source | SpringerLink Journals - AutoHoldings |
subjects | Ammonium compounds Aromatic compounds Chemistry Chemistry and Materials Science Chemistry/Food Science Reagents Self-assembly |
title | Novel Acylhydrazones Based on 1-Decylisatins and Girard Reagent T Possessing Antimicrobial Activity |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T15%3A59%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20Acylhydrazones%20Based%20on%201-Decylisatins%20and%20Girard%20Reagent%20T%20Possessing%20Antimicrobial%20Activity&rft.jtitle=Russian%20journal%20of%20general%20chemistry&rft.au=Bogdanov,%20A.%20V.&rft.date=2024-11-01&rft.volume=94&rft.issue=11&rft.spage=3099&rft.epage=3103&rft.pages=3099-3103&rft.issn=1070-3632&rft.eissn=1608-3350&rft_id=info:doi/10.1134/S1070363224110331&rft_dat=%3Cproquest_cross%3E3146496795%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3146496795&rft_id=info:pmid/&rfr_iscdi=true |