Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm

There is a pressing need to develop new antimicrobials to help combat the increase in antibiotic resistance that is occurring worldwide. In the current research, short amphiphilic antibacterial and antibiofilm agents were produced by tuning the hydrophobic and cationic groups of anthranilamide pepti...
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Autor*in:	Rajesh Kuppusamy [verfasserIn] Muhammad Yasir [verfasserIn] Tsz Tin Yu [verfasserIn] Florida Voli [verfasserIn] Orazio Vittorio [verfasserIn] Michael J. Miller [verfasserIn] Peter Lewis [verfasserIn] David StC Black [verfasserIn] Mark Willcox [verfasserIn] Naresh Kumar [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2023

Schlagwörter:	peptidomimetics biofilm anthranilamide

Übergeordnetes Werk:	In: Antibiotics - MDPI AG, 2013, 12(2023), 3, p 585
Übergeordnetes Werk:	volume:12 ; year:2023 ; number:3, p 585

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.3390/antibiotics12030585

Katalog-ID:	DOAJ087450534

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allfieldsSound	10.3390/antibiotics12030585 doi (DE-627)DOAJ087450534 (DE-599)DOAJ7e6a6aceea644ab5b17e529e28105b80 DE-627 ger DE-627 rakwb eng RM1-950 Rajesh Kuppusamy verfasserin aut Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier There is a pressing need to develop new antimicrobials to help combat the increase in antibiotic resistance that is occurring worldwide. In the current research, short amphiphilic antibacterial and antibiofilm agents were produced by tuning the hydrophobic and cationic groups of anthranilamide peptidomimetics. The attachment of a lysine cationic group at the tail position increased activity against <i<E. coli</i< by <16-fold (from <125 μM to 15.6 μM) and greatly reduced cytotoxicity against mammalian cells (from ≤20 μM to ≥150 μM). These compounds showed significant disruption of preformed biofilms of <i<S. aureus</i< at micromolar concentrations. peptidomimetics biofilm anthranilamide Therapeutics. Pharmacology Muhammad Yasir verfasserin aut Tsz Tin Yu verfasserin aut Florida Voli verfasserin aut Orazio Vittorio verfasserin aut Michael J. Miller verfasserin aut Peter Lewis verfasserin aut David StC Black verfasserin aut Mark Willcox verfasserin aut Naresh Kumar verfasserin aut In Antibiotics MDPI AG, 2013 12(2023), 3, p 585 (DE-627)726120596 (DE-600)2681345-2 20796382 nnns volume:12 year:2023 number:3, p 585 https://doi.org/10.3390/antibiotics12030585 kostenfrei https://doaj.org/article/7e6a6aceea644ab5b17e529e28105b80 kostenfrei https://www.mdpi.com/2079-6382/12/3/585 kostenfrei https://doaj.org/toc/2079-6382 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 3, p 585
language	English
source	In Antibiotics 12(2023), 3, p 585 volume:12 year:2023 number:3, p 585
sourceStr	In Antibiotics 12(2023), 3, p 585 volume:12 year:2023 number:3, p 585
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	peptidomimetics biofilm anthranilamide Therapeutics. Pharmacology
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container_title	Antibiotics
authorswithroles_txt_mv	Rajesh Kuppusamy @@aut@@ Muhammad Yasir @@aut@@ Tsz Tin Yu @@aut@@ Florida Voli @@aut@@ Orazio Vittorio @@aut@@ Michael J. Miller @@aut@@ Peter Lewis @@aut@@ David StC Black @@aut@@ Mark Willcox @@aut@@ Naresh Kumar @@aut@@
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callnumber-first	R - Medicine
author	Rajesh Kuppusamy
spellingShingle	Rajesh Kuppusamy misc RM1-950 misc peptidomimetics misc biofilm misc anthranilamide misc Therapeutics. Pharmacology Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm
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topic_title	RM1-950 Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm peptidomimetics biofilm anthranilamide
topic	misc RM1-950 misc peptidomimetics misc biofilm misc anthranilamide misc Therapeutics. Pharmacology
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title	Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm
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title_full	Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm
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title_auth	Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm
abstract	There is a pressing need to develop new antimicrobials to help combat the increase in antibiotic resistance that is occurring worldwide. In the current research, short amphiphilic antibacterial and antibiofilm agents were produced by tuning the hydrophobic and cationic groups of anthranilamide peptidomimetics. The attachment of a lysine cationic group at the tail position increased activity against <i<E. coli</i< by <16-fold (from <125 μM to 15.6 μM) and greatly reduced cytotoxicity against mammalian cells (from ≤20 μM to ≥150 μM). These compounds showed significant disruption of preformed biofilms of <i<S. aureus</i< at micromolar concentrations.
abstractGer	There is a pressing need to develop new antimicrobials to help combat the increase in antibiotic resistance that is occurring worldwide. In the current research, short amphiphilic antibacterial and antibiofilm agents were produced by tuning the hydrophobic and cationic groups of anthranilamide peptidomimetics. The attachment of a lysine cationic group at the tail position increased activity against <i<E. coli</i< by <16-fold (from <125 μM to 15.6 μM) and greatly reduced cytotoxicity against mammalian cells (from ≤20 μM to ≥150 μM). These compounds showed significant disruption of preformed biofilms of <i<S. aureus</i< at micromolar concentrations.
abstract_unstemmed	There is a pressing need to develop new antimicrobials to help combat the increase in antibiotic resistance that is occurring worldwide. In the current research, short amphiphilic antibacterial and antibiofilm agents were produced by tuning the hydrophobic and cationic groups of anthranilamide peptidomimetics. The attachment of a lysine cationic group at the tail position increased activity against <i<E. coli</i< by <16-fold (from <125 μM to 15.6 μM) and greatly reduced cytotoxicity against mammalian cells (from ≤20 μM to ≥150 μM). These compounds showed significant disruption of preformed biofilms of <i<S. aureus</i< at micromolar concentrations.
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title_short	Tuning the Anthranilamide Peptidomimetic Design to Selectively Target Planktonic Bacteria and Biofilm
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