Loading…
Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteriaElectronic supplementary information (ESI) available. ESI and CCDC 1819893 and 1819894. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c9nj00563c
Selenocyanates represent an interesting class of organic selenium compounds. Due to their similarity with better known natural (iso-)thiocyanates, they promise high biological activity and may also be metabolized to other Reactive Selenium Species (RSeS), such as selenols, diselenides and seleninic...
Saved in:
| Main Authors: | , , , , , , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Online Access: | Get full text |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| cited_by | |
|---|---|
| cites | |
| container_end_page | 631 |
| container_issue | 15 |
| container_start_page | 621 |
| container_title | |
| container_volume | 43 |
| creator | Nasim, Muhammad Jawad Witek, Karolina Kincses, Annamária Abdin, Ahmad Yaman es awska, Ewa Mar, Ma gorzata Anna Gajdács, Márió Spengler, Gabriella Nitek, Wojciech Latacz, Gniewomir Karczewska, El bieta Kie -Kononowicz, Katarzyna Handzlik, Jadwiga Jacob, Claus |
| description | Selenocyanates represent an interesting class of organic selenium compounds. Due to their similarity with better known natural (iso-)thiocyanates, they promise high biological activity and may also be metabolized to other Reactive Selenium Species (RSeS), such as selenols, diselenides and seleninic acids. Thirteen arylmethyl selenocyanates (
1-13
) have been synthesized and evaluated for potential antimicrobial, nematicidal and cytotoxic activity. The compounds exhibit pronounced antimicrobial activity against various strains of Gram-positive and Gram-negative bacteria and yeasts, including multidrug resistant strains. The results obtained so far demonstrate that these arylmethyl selenocyanates are also non-mutagenic and have limited cytotoxicity against human cells. Here, benzyl selenocyanate (
1
) represents the most active anti-ESKAPE agent, with potent activity against multidrug resistant MRSA strains (HEMSA 5) - with a competitive MIC value of just 0.76 μg mL
−1
(3.88 μM), whereas it exhibits low(er) cytotoxicity (IC
50
= 31 μM) and no mutagenicity against mammalian cells. Due to this selective antimicrobial activity, aromatic selenocyanates may provide an interesting lead in the development of antimicrobial agents, particularly in the context of drug resistance.
Selenocyanates demonstrate pronounced activity against bacteria of the ESKAPE family, yeast and nematodes with limited cytotoxicity against human cells. |
| doi_str_mv | 10.1039/c9nj00563c |
| format | article |
| fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c9nj00563c</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c9nj00563c</sourcerecordid><originalsourceid>FETCH-rsc_primary_c9nj00563c3</originalsourceid><addsrcrecordid>eNqFkEFLw0AQhVdRsFYv3oXxpofWrEmj8SZpisGDhXov082kXdnsht1NIf_erRV6EPQ0w8zje2-GsSsejXkUZ_ci059RNEljccwGPE6zUfaQ8pPQ8yQZRZMkPWPnzgUN548pHxwN5tZo02lBFaDwcit9D6YGtKZBLwU4UqSN6FGjJwe4Rqmdh6ZTXla2W4MlJ51H7aFYvL3MC1gFDlmJhSLhA30H6dpWUUPao-1B6trYHd1ouC0W5R3gFqXClaJxgJSAuoI8n-bAn3j2lMXfg32fjGFmLAjbB0-lzNpiuwkOFXoMYMjLGYS98RuyQIcEe8dwDcH0vXyG3w-7YKc1KkeXP3XIrmfFR_46sk4sWyubEH15kMdDdvPXftlWdfwf4wvWfImI</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteriaElectronic supplementary information (ESI) available. ESI and CCDC 1819893 and 1819894. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c9nj00563c</title><source>Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)</source><creator>Nasim, Muhammad Jawad ; Witek, Karolina ; Kincses, Annamária ; Abdin, Ahmad Yaman ; es awska, Ewa ; Mar, Ma gorzata Anna ; Gajdács, Márió ; Spengler, Gabriella ; Nitek, Wojciech ; Latacz, Gniewomir ; Karczewska, El bieta ; Kie -Kononowicz, Katarzyna ; Handzlik, Jadwiga ; Jacob, Claus</creator><creatorcontrib>Nasim, Muhammad Jawad ; Witek, Karolina ; Kincses, Annamária ; Abdin, Ahmad Yaman ; es awska, Ewa ; Mar, Ma gorzata Anna ; Gajdács, Márió ; Spengler, Gabriella ; Nitek, Wojciech ; Latacz, Gniewomir ; Karczewska, El bieta ; Kie -Kononowicz, Katarzyna ; Handzlik, Jadwiga ; Jacob, Claus</creatorcontrib><description>Selenocyanates represent an interesting class of organic selenium compounds. Due to their similarity with better known natural (iso-)thiocyanates, they promise high biological activity and may also be metabolized to other Reactive Selenium Species (RSeS), such as selenols, diselenides and seleninic acids. Thirteen arylmethyl selenocyanates (
1-13
) have been synthesized and evaluated for potential antimicrobial, nematicidal and cytotoxic activity. The compounds exhibit pronounced antimicrobial activity against various strains of Gram-positive and Gram-negative bacteria and yeasts, including multidrug resistant strains. The results obtained so far demonstrate that these arylmethyl selenocyanates are also non-mutagenic and have limited cytotoxicity against human cells. Here, benzyl selenocyanate (
1
) represents the most active anti-ESKAPE agent, with potent activity against multidrug resistant MRSA strains (HEMSA 5) - with a competitive MIC value of just 0.76 μg mL
−1
(3.88 μM), whereas it exhibits low(er) cytotoxicity (IC
50
= 31 μM) and no mutagenicity against mammalian cells. Due to this selective antimicrobial activity, aromatic selenocyanates may provide an interesting lead in the development of antimicrobial agents, particularly in the context of drug resistance.
Selenocyanates demonstrate pronounced activity against bacteria of the ESKAPE family, yeast and nematodes with limited cytotoxicity against human cells.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c9nj00563c</identifier><language>eng</language><creationdate>2019-04</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,786,790,27957,27958</link.rule.ids></links><search><creatorcontrib>Nasim, Muhammad Jawad</creatorcontrib><creatorcontrib>Witek, Karolina</creatorcontrib><creatorcontrib>Kincses, Annamária</creatorcontrib><creatorcontrib>Abdin, Ahmad Yaman</creatorcontrib><creatorcontrib>es awska, Ewa</creatorcontrib><creatorcontrib>Mar, Ma gorzata Anna</creatorcontrib><creatorcontrib>Gajdács, Márió</creatorcontrib><creatorcontrib>Spengler, Gabriella</creatorcontrib><creatorcontrib>Nitek, Wojciech</creatorcontrib><creatorcontrib>Latacz, Gniewomir</creatorcontrib><creatorcontrib>Karczewska, El bieta</creatorcontrib><creatorcontrib>Kie -Kononowicz, Katarzyna</creatorcontrib><creatorcontrib>Handzlik, Jadwiga</creatorcontrib><creatorcontrib>Jacob, Claus</creatorcontrib><title>Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteriaElectronic supplementary information (ESI) available. ESI and CCDC 1819893 and 1819894. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c9nj00563c</title><description>Selenocyanates represent an interesting class of organic selenium compounds. Due to their similarity with better known natural (iso-)thiocyanates, they promise high biological activity and may also be metabolized to other Reactive Selenium Species (RSeS), such as selenols, diselenides and seleninic acids. Thirteen arylmethyl selenocyanates (
1-13
) have been synthesized and evaluated for potential antimicrobial, nematicidal and cytotoxic activity. The compounds exhibit pronounced antimicrobial activity against various strains of Gram-positive and Gram-negative bacteria and yeasts, including multidrug resistant strains. The results obtained so far demonstrate that these arylmethyl selenocyanates are also non-mutagenic and have limited cytotoxicity against human cells. Here, benzyl selenocyanate (
1
) represents the most active anti-ESKAPE agent, with potent activity against multidrug resistant MRSA strains (HEMSA 5) - with a competitive MIC value of just 0.76 μg mL
−1
(3.88 μM), whereas it exhibits low(er) cytotoxicity (IC
50
= 31 μM) and no mutagenicity against mammalian cells. Due to this selective antimicrobial activity, aromatic selenocyanates may provide an interesting lead in the development of antimicrobial agents, particularly in the context of drug resistance.
Selenocyanates demonstrate pronounced activity against bacteria of the ESKAPE family, yeast and nematodes with limited cytotoxicity against human cells.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkEFLw0AQhVdRsFYv3oXxpofWrEmj8SZpisGDhXov082kXdnsht1NIf_erRV6EPQ0w8zje2-GsSsejXkUZ_ci059RNEljccwGPE6zUfaQ8pPQ8yQZRZMkPWPnzgUN548pHxwN5tZo02lBFaDwcit9D6YGtKZBLwU4UqSN6FGjJwe4Rqmdh6ZTXla2W4MlJ51H7aFYvL3MC1gFDlmJhSLhA30H6dpWUUPao-1B6trYHd1ouC0W5R3gFqXClaJxgJSAuoI8n-bAn3j2lMXfg32fjGFmLAjbB0-lzNpiuwkOFXoMYMjLGYS98RuyQIcEe8dwDcH0vXyG3w-7YKc1KkeXP3XIrmfFR_46sk4sWyubEH15kMdDdvPXftlWdfwf4wvWfImI</recordid><startdate>20190408</startdate><enddate>20190408</enddate><creator>Nasim, Muhammad Jawad</creator><creator>Witek, Karolina</creator><creator>Kincses, Annamária</creator><creator>Abdin, Ahmad Yaman</creator><creator>es awska, Ewa</creator><creator>Mar, Ma gorzata Anna</creator><creator>Gajdács, Márió</creator><creator>Spengler, Gabriella</creator><creator>Nitek, Wojciech</creator><creator>Latacz, Gniewomir</creator><creator>Karczewska, El bieta</creator><creator>Kie -Kononowicz, Katarzyna</creator><creator>Handzlik, Jadwiga</creator><creator>Jacob, Claus</creator><scope/></search><sort><creationdate>20190408</creationdate><title>Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteriaElectronic supplementary information (ESI) available. ESI and CCDC 1819893 and 1819894. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c9nj00563c</title><author>Nasim, Muhammad Jawad ; Witek, Karolina ; Kincses, Annamária ; Abdin, Ahmad Yaman ; es awska, Ewa ; Mar, Ma gorzata Anna ; Gajdács, Márió ; Spengler, Gabriella ; Nitek, Wojciech ; Latacz, Gniewomir ; Karczewska, El bieta ; Kie -Kononowicz, Katarzyna ; Handzlik, Jadwiga ; Jacob, Claus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c9nj00563c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nasim, Muhammad Jawad</creatorcontrib><creatorcontrib>Witek, Karolina</creatorcontrib><creatorcontrib>Kincses, Annamária</creatorcontrib><creatorcontrib>Abdin, Ahmad Yaman</creatorcontrib><creatorcontrib>es awska, Ewa</creatorcontrib><creatorcontrib>Mar, Ma gorzata Anna</creatorcontrib><creatorcontrib>Gajdács, Márió</creatorcontrib><creatorcontrib>Spengler, Gabriella</creatorcontrib><creatorcontrib>Nitek, Wojciech</creatorcontrib><creatorcontrib>Latacz, Gniewomir</creatorcontrib><creatorcontrib>Karczewska, El bieta</creatorcontrib><creatorcontrib>Kie -Kononowicz, Katarzyna</creatorcontrib><creatorcontrib>Handzlik, Jadwiga</creatorcontrib><creatorcontrib>Jacob, Claus</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nasim, Muhammad Jawad</au><au>Witek, Karolina</au><au>Kincses, Annamária</au><au>Abdin, Ahmad Yaman</au><au>es awska, Ewa</au><au>Mar, Ma gorzata Anna</au><au>Gajdács, Márió</au><au>Spengler, Gabriella</au><au>Nitek, Wojciech</au><au>Latacz, Gniewomir</au><au>Karczewska, El bieta</au><au>Kie -Kononowicz, Katarzyna</au><au>Handzlik, Jadwiga</au><au>Jacob, Claus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteriaElectronic supplementary information (ESI) available. ESI and CCDC 1819893 and 1819894. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c9nj00563c</atitle><date>2019-04-08</date><risdate>2019</risdate><volume>43</volume><issue>15</issue><spage>621</spage><epage>631</epage><pages>621-631</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><notes>and</notes><notes>For crystallographic data in CIF or other electronic format see DOI</notes><notes>1819894</notes><notes>10.1039/c9nj00563c</notes><notes>Electronic supplementary information (ESI) available. ESI and CCDC</notes><notes>1819893</notes><abstract>Selenocyanates represent an interesting class of organic selenium compounds. Due to their similarity with better known natural (iso-)thiocyanates, they promise high biological activity and may also be metabolized to other Reactive Selenium Species (RSeS), such as selenols, diselenides and seleninic acids. Thirteen arylmethyl selenocyanates (
1-13
) have been synthesized and evaluated for potential antimicrobial, nematicidal and cytotoxic activity. The compounds exhibit pronounced antimicrobial activity against various strains of Gram-positive and Gram-negative bacteria and yeasts, including multidrug resistant strains. The results obtained so far demonstrate that these arylmethyl selenocyanates are also non-mutagenic and have limited cytotoxicity against human cells. Here, benzyl selenocyanate (
1
) represents the most active anti-ESKAPE agent, with potent activity against multidrug resistant MRSA strains (HEMSA 5) - with a competitive MIC value of just 0.76 μg mL
−1
(3.88 μM), whereas it exhibits low(er) cytotoxicity (IC
50
= 31 μM) and no mutagenicity against mammalian cells. Due to this selective antimicrobial activity, aromatic selenocyanates may provide an interesting lead in the development of antimicrobial agents, particularly in the context of drug resistance.
Selenocyanates demonstrate pronounced activity against bacteria of the ESKAPE family, yeast and nematodes with limited cytotoxicity against human cells.</abstract><doi>10.1039/c9nj00563c</doi><tpages>11</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1144-0546 |
| ispartof | |
| issn | 1144-0546 1369-9261 |
| language | eng |
| recordid | cdi_rsc_primary_c9nj00563c |
| source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
| title | Pronounced activity of aromatic selenocyanates against multidrug resistant ESKAPE bacteriaElectronic supplementary information (ESI) available. ESI and CCDC 1819893 and 1819894. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c9nj00563c |
| url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-09-21T18%3A06%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pronounced%20activity%20of%20aromatic%20selenocyanates%20against%20multidrug%20resistant%20ESKAPE%20bacteriaElectronic%20supplementary%20information%20(ESI)%20available.%20ESI%20and%20CCDC%201819893%20and%201819894.%20For%20crystallographic%20data%20in%20CIF%20or%20other%20electronic%20format%20see%20DOI:%2010.1039/c9nj00563c&rft.au=Nasim,%20Muhammad%20Jawad&rft.date=2019-04-08&rft.volume=43&rft.issue=15&rft.spage=621&rft.epage=631&rft.pages=621-631&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/c9nj00563c&rft_dat=%3Crsc%3Ec9nj00563c%3C/rsc%3E%3Cgrp_id%3Ecdi_FETCH-rsc_primary_c9nj00563c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |