This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Balgavý P. Devínsky F. Cut-off effects in biological activities of surfactants. Adv Colloid Interface Sci. 1996;66:23–63.BalgavýPDevínskyFCut-off effects in biological activities of surfactantsAdv Colloid Interface Sci199666236310.1016/0001-8686(96)00295-3Search in Google Scholar
Benkova M. Soukup O. Prchal L. et al. Synthesis, antimicrobial effect and lipophilicity-activity dependence of three series of dichained N-alkylammonium salts. Chemistry 2019;4:12076–12084.BenkovaMSoukupOPrchalLSynthesis, antimicrobial effect and lipophilicity-activity dependence of three series of dichained N-alkylammonium saltsChemistry20194120761208410.1002/slct.201902357Search in Google Scholar
Birnie CR. Malamud D. Schnaare RL. Antimicrobial evaluation of N-alkyl betaines and N-alkyl-N,N-dimethylamine oxides with variations in chain length. Antimicrob Agents Chemother. 2000;44:2514–2517.BirnieCRMalamudDSchnaareRLAntimicrobial evaluation of N-alkyl betaines and N-alkyl-N,N-dimethylamine oxides with variations in chain lengthAntimicrob Agents Chemother2000442514251710.1128/AAC.44.9.2514-2517.20009009410952604Search in Google Scholar
Brak K. Jacobsen EN. Asymmetric ion-pairing catalysis. Angew Chem Int Ed. 2013;52(2):534–561.BrakKJacobsenENAsymmetric ion-pairing catalysisAngew Chem Int Ed201352253456110.1002/anie.201205449428495123192886Search in Google Scholar
Brigham KL. Mezrick B. Christman B. Magnuson M. King G. Berry LC. In vivo Transfection of Murine Lungs with a Functioning Prokaryotic Gene Using a Liposome Vehicle. Am J Med Sci. 1989; 298: 278–281.BrighamKLMezrickBChristmanBMagnusonMKingGBerryLCIn vivo Transfection of Murine Lungs with a Functioning Prokaryotic Gene Using a Liposome VehicleAm J Med Sci198929827828110.1097/00000441-198910000-000132801762Search in Google Scholar
Bureš F. Quaternary Ammonium Compounds: Simple in Structure, Complex in Application. Top Curr Chem. 2019;377:14.BurešFQuaternary Ammonium Compounds: Simple in Structure, Complex in ApplicationTop Curr Chem20193771410.1007/s41061-019-0239-231062103Search in Google Scholar
Cortesi R. Bergamini P. Ravani L. et al. Long-chain cationic derivatives of PTA (1,3,5-triaza-7-phosphaadamantane) as new components of potential non-viral vectors. Int J Pharm. 2012; 431:176–182.CortesiRBergaminiPRavaniLLong-chain cationic derivatives of PTA (1,3,5-triaza-7-phosphaadamantane) as new components of potential non-viral vectorsInt J Pharm201243117618210.1016/j.ijpharm.2012.04.01422513391Search in Google Scholar
Denyer SP Hugo WB. The mode of action of cetyltrimethylammonium bromide (CTAB) on Staphylococcus aureus. J Pharm Pharmacol. 1977;29:66P.DenyerSPHugoWBThe mode of action of cetyltrimethylammonium bromide (CTAB) on Staphylococcus aureusJ Pharm Pharmacol19772966P10.1111/j.2042-7158.1977.tb11534.x22699Search in Google Scholar
Devínsky F. Lacko I. Mlynarčík D. Račanský V. Krasnec Ľ. Relationship between critical micelle concentrations and minimum inhibitory concentrations for some non-aromatic quaternary ammonium salts and amine oxides. Tenside Deterg. 1985;22:10–15.DevínskyFLackoIMlynarčíkDRačanskýVKrasnecĽRelationship between critical micelle concentrations and minimum inhibitory concentrations for some non-aromatic quaternary ammonium salts and amine oxidesTenside Deterg198522101510.1515/tsd-1985-220105Search in Google Scholar
Eagles JB. Hitchcock SR. Synthesis of D-camphor based γ-amino acid (1S,3R)-3-amino-2,2,3-trimethylcyclopentane carboxylic acid. Tetrahedron: Asymmetry. 2010;21(5):519–523.EaglesJBHitchcockSRSynthesis of D-camphor based γ-amino acid (1S,3R)-3-amino-2,2,3-trimethylcyclopentane carboxylic acidTetrahedron: Asymmetry201021551952310.1016/j.tetasy.2010.03.022Search in Google Scholar
Feder-Kubis J. Tomczuk K. The effect of the cationic structures of chiral ionic liquids on their antimicrobial activities. Tetrahedron 2013;69(21):4190–4198.Feder-KubisJTomczukKThe effect of the cationic structures of chiral ionic liquids on their antimicrobial activitiesTetrahedron201369214190419810.1016/j.tet.2013.03.107Search in Google Scholar
Gilbert P. Moore LE. Cationic antiseptics: diversity of action under a common Epithet. J. Appl Microbiol 2005; 99: 703–715.GilbertPMooreLECationic antiseptics: diversity of action under a common EpithetJ. Appl Microbiol20059970371510.1111/j.1365-2672.2005.02664.x16162221Search in Google Scholar
Jennings MC. Minbiole KPC. Wuest WM. Quaternary Ammonium Compounds: An Antimicrobial Mainstay and Platform for Innovation to Address Bacterial Resistance. ACS Infect Dis. 2015;1:288–303.JenningsMCMinbioleKPCWuestWMQuaternary Ammonium Compounds: An Antimicrobial Mainstay and Platform for Innovation to Address Bacterial ResistanceACS Infect Dis2015128830310.1021/acsinfecdis.5b0004727622819Search in Google Scholar
Joondan N. Jhaumeer-Laulloo S. Caumul P. A study of the antibacterial activity of L-Phenylalanine and L-Tyrosine esters in relation to their CMCs and their interactions with 1,2-dipalmitoylsn-glycero-3-phosphocholine, DPPC as model membrane. Microbiol Res. 2014;169:657–685.JoondanNJhaumeer-LaullooSCaumulPA study of the antibacterial activity of L-Phenylalanine and L-Tyrosine esters in relation to their CMCs and their interactions with 1,2-dipalmitoylsn-glycero-3-phosphocholine, DPPC as model membraneMicrobiol Res201416965768510.1016/j.micres.2014.02.01024667307Search in Google Scholar
Kaushik NK, Attri P, Kaushik N, Choi EH. Synthesis and Antiproliferative Activity of Ammonium and Imidazolium Ionic Liquids against T98G Brain Cancer Cells. Molecules 2012;17(12):13727–13739.KaushikNKAttriPKaushikNChoiEHSynthesis and Antiproliferative Activity of Ammonium and Imidazolium Ionic Liquids against T98G Brain Cancer CellsMolecules20121712137271373910.3390/molecules171213727626855023174892Search in Google Scholar
Kim YH. Sun G. Functional Finishing of Acrylic and Cationic Dyeable Fabrics: Intermolecular Interactions. Text Res J. 2002; 72: 1052–1056.KimYHSunGFunctional Finishing of Acrylic and Cationic Dyeable Fabrics: Intermolecular InteractionsText Res J2002721052105610.1177/004051750207201203Search in Google Scholar
Klevens HB. Structure and aggregation in divte solutions of surface aktive agents. J Am Oil Chem Soc. 1953;30:74–80.KlevensHBStructure and aggregation in divte solutions of surface aktive agentsJ Am Oil Chem Soc195330748010.1007/BF02635002Search in Google Scholar
Kopecká-Leitmanová A. Devinsky F. Mlynarčík D. Lacko I. Interaction of amine oxides and quaternary ammonium salts with membrane and membrane-associated processes in E. Coli cells: mode of action. Drug Metabol Drug Interact. 1989;7(1):29–51.Kopecká-LeitmanováADevinskyFMlynarčíkDLackoIInteraction of amine oxides and quaternary ammonium salts with membrane and membrane-associated processes in E. Coli cells: mode of actionDrug Metabol Drug Interact198971295110.1515/DMDI.1989.7.1.292699283Search in Google Scholar
Lukáč M, Lacko I, Bukovský M et al. Synthesis and antimicrobial activity of a series of optically active quaternary ammonium salts derived from phenylalanine. Cent Eur J Chem. 2010;8:194–201.LukáčMLackoIBukovskýMSynthesis and antimicrobial activity of a series of optically active quaternary ammonium salts derived from phenylalanineCent Eur J Chem2010819420110.2478/s11532-009-0126-8Search in Google Scholar
Malinak D. Dolezal R. Marek J. et al. 6-Hydroxyquinolinium salts differing in the length of alkyl side-chain: synthesis and antimicrobial activity. Bioorg Med Chem Lett. 2014;24:5238–5241.MalinakDDolezalRMarekJ6-Hydroxyquinolinium salts differing in the length of alkyl side-chain: synthesis and antimicrobial activityBioorg Med Chem Lett2014245238524110.1016/j.bmcl.2014.09.06025442318Search in Google Scholar
Marek J. Joskova V. Dolezal R. et al. Synthesis, antimicrobial effect and surface properties of hydroxymethyl-substituted pyridinium salts. Lett Drug Des Discov. 2018;15:828–842.MarekJJoskovaVDolezalRSynthesis, antimicrobial effect and surface properties of hydroxymethyl-substituted pyridinium saltsLett Drug Des Discov20181582884210.2174/1570180814666171110142233Search in Google Scholar
Menzel TM. Tischer M. Francois P. et al. Mode-of-Action studies of the Novel Bisquaternary Bisnaphthalimide MT02 against Staphylococcus aureus. Antimicrob Agents Chemother. 2011;55:311–320.MenzelTMTischerMFrancoisPMode-of-Action studies of the Novel Bisquaternary Bisnaphthalimide MT02 against Staphylococcus aureusAntimicrob Agents Chemother20115531132010.1128/AAC.00586-10Search in Google Scholar
Merianos JJ. Quaternary ammonium antimicrobial compounds. In Disinfection, sterilization, and preservation, 4th Edition, 1991, Lea & Febiger, Philadelphia. ISBN: 0-8121-1364-0.MerianosJJQuaternary ammonium antimicrobial compoundsInDisinfection, sterilization, and preservation4th Edition1991Lea & FebigerPhiladelphiaISBN: 0-8121-1364-0.Search in Google Scholar
Miguel G. Cruz C. Faleiro ML. Simoes MTF. Figueiredo AC. Barroso JG. Pedro LG. Salvia officinalis L. essential oils: effect of hydrodistillation time on the chemical composition, antioxidant and antimicrobial activities. Nat Prod Res. 2011;25(5):526–541.MiguelGCruzCFaleiroMLSimoesMTFFigueiredoACBarrosoJGPedroLGSalvia officinalis L. essential oils: effect of hydrodistillation time on the chemical composition, antioxidant and antimicrobial activitiesNat Prod Res201125552654110.1080/14786419.2010.499513Search in Google Scholar
Mikláš R, Miklášová N, Bukovský M, Devínsky F. Synthesis and antimicrobial properties of binaphthyl derived quaternary ammonium bromides. Acta Facult Pharm Univ Comenianae. 2012;59:39–47.MiklášRMiklášováNBukovskýMDevínskyFSynthesis and antimicrobial properties of binaphthyl derived quaternary ammonium bromidesActa Facult Pharm Univ Comenianae201259394710.2478/v10219-012-0017-5Search in Google Scholar
Mikláš R, Miklášová N, Bukovský M, Horváth B, Kubincová J, Devínsky F. Synthesis, surface and antimicrobial properties of some quaternary ammonium homochiral camphor sulfonamides. Eur J Pharm Sci. 2014;65:29–37.MiklášRMiklášováNBukovskýMHorváthBKubincováJDevínskyFSynthesis, surface and antimicrobial properties of some quaternary ammonium homochiral camphor sulfonamidesEur J Pharm Sci201465293710.1016/j.ejps.2014.08.013Search in Google Scholar
Mlynarčík D. Denyer SP. Hugo WB. A study of the action of a bisquaternary ammonium salt, an amine oxide and an alkoxy phenylcarbamic acid ester on some metabolic functions in Staphylococcus aureus. Microbios 1981;30:27–35.MlynarčíkDDenyerSPHugoWBA study of the action of a bisquaternary ammonium salt, an amine oxide and an alkoxy phenylcarbamic acid ester on some metabolic functions in Staphylococcus aureusMicrobios1981302735Search in Google Scholar
Morel A. Silarska E. Trzeciak A M. Pernak J. Palladium-catalyzed asymmetric Heck arylation of 2,3-dihydrofuran – effect of prolinate salts. Dalton Trans. 2013; 42(4): 1215–1222.MorelASilarskaETrzeciak AMPernakJPalladium-catalyzed asymmetric Heck arylation of 2,3-dihydrofuran – effect of prolinate saltsDalton Trans20134241215122210.1039/C2DT31672BSearch in Google Scholar
Pérez L. Pinazo A. García MT et al. Cationic surfactants from lysine: Synthesis, micellization and biological evaluation. Eur J Med Chem. 2009;44:1884–1892.PérezLPinazoAGarcíaMTCationic surfactants from lysine: Synthesis, micellization and biological evaluationEur J Med Chem2009441884189210.1016/j.ejmech.2008.11.003Search in Google Scholar
Pernak J. Skrzypczak A. 3-Alkylthiomethyl-1-ethylimidazolium chlorides. Correlation between critical micelle concentrations and minimum inhibitory concentrations. Eur J Med Chem. 1996;31:901–903.PernakJSkrzypczakA3-Alkylthiomethyl-1-ethylimidazolium chlorides. Correlation between critical micelle concentrations and minimum inhibitory concentrationsEur J Med Chem19963190190310.1016/S0223-5234(97)89853-4Search in Google Scholar
Pernak J. Kalewska J. Ksycińska H. Cybulski J. Synthesis and antimicrobial activities of some pyridinium salts with alkoxymethyl hydrophobic group. Eur J Med Chem. 2001;36:899–907.PernakJKalewskaJKsycińskaHCybulskiJSynthesis and antimicrobial activities of some pyridinium salts with alkoxymethyl hydrophobic groupEur J Med Chem20013689990710.1016/S0223-5234(01)01280-6Search in Google Scholar
Piętka-Ottlik M., Frąckowiak R., Maliszewska I., Kołwzan B., Wilk KA. Ecotoxicity and biodegradability of antielectrostatic dicephalic cationic surfactants. Chemosphere 2012; 89: 1103–1111.Piętka-OttlikM, FrąckowiakR.MaliszewskaI.KołwzanB.WilkKAEcotoxicity and biodegradability of antielectrostatic dicephalic cationic surfactantsChemosphere2012891103111110.1016/j.chemosphere.2012.05.09022743183Search in Google Scholar
Rice LM. Grogan CH. Hypotensive agents VI. Substitued 3-Azabicyclo[3.2.1]octane derivates. J Org Chem. 1957;22:185–189.RiceLMGroganCHHypotensive agents VI. Substitued 3-Azabicyclo[3.2.1]octane derivatesJ Org Chem19572218518910.1021/jo01353a025Search in Google Scholar
Rosen MJ. Surfactants and interfacial phenomena, 2nd Edition, New York, John Wiley & Sons. ISBN: 0-471-83651-6; 1989.RosenMJSurfactants and interfacial phenomena2nd EditionNew YorkJohn Wiley & SonsISBN: 0-471-83651-6;1989Search in Google Scholar
Ruiz-Navajas Y. Viuda-Martos M. Sendra M. Perez-Alvarez JA. Fernandez-Lopez J. Chemical characterization and antibacterial activity of Thymus moroderi and Thymus piperella essential oils, two Thymus endemic species from southeast of Spain. Food Control 2012;27(2):294–299.Ruiz-NavajasYViuda-MartosMSendraMPerez-AlvarezJAFernandez-LopezJChemical characterization and antibacterial activity of Thymus moroderi and Thymus piperella essential oils, two Thymus endemic species from southeast of SpainFood Control201227229429910.1016/j.foodcont.2012.04.005Search in Google Scholar
Sajomsang W. Gonil P. Ruktanonchai UR. Petchsangsai M. Opanasopit P. Puttipipatkhachorn S. Effects of molecular weight and pyridinium moiety on water-soluble chitosan derivatives for mediated gene delivery. Carbohydr Polym. 2013; 91(2): 508–517.SajomsangWGonilPRuktanonchaiURPetchsangsaiMOpanasopitPPuttipipatkhachornSEffects of molecular weight and pyridinium moiety on water-soluble chitosan derivatives for mediated gene deliveryCarbohydr Polym201391250851710.1016/j.carbpol.2012.08.053Search in Google Scholar
Schrank CL. Minbiole KPC. Wuest WM. Are Quaternary Ammonium Compounds, the Workhorse Disinfectants, effective against Severe Acute Respiratory Syndrome-Coronavirus-2? ACS Infect Dis. 2020;6(7):1553–1557.SchrankCLMinbioleKPCWuestWMAre Quaternary Ammonium Compounds, the Workhorse Disinfectants, effective against Severe Acute Respiratory Syndrome-Coronavirus-2?ACS Infect Dis2020671553155710.1021/acsinfecdis.0c00265Search in Google Scholar
Semenov VE. Mikhailov AS. Voloshina AD. Et al. Antimicrobial activity of pyrimidinophanes with thiocytosine and uracil moieties. Eur J Med Chem 2011;46(9):4715–4724.SemenovVEMikhailovASVoloshinaADAntimicrobial activity of pyrimidinophanes with thiocytosine and uracil moietiesEur J Med Chem20114694715472410.1016/j.ejmech.2011.05.034Search in Google Scholar
Shirakawa S. Liu K. Maruoka K. Catalytic Asymmetric Synthesis of Axially Chiral o-Iodoanilides by Phase-Transfer Catalyzed Alkylations. J Am Chem Soc. 2012; 134(2): 916–919.ShirakawaSLiuKMaruokaKCatalytic Asymmetric Synthesis of Axially Chiral o-Iodoanilides by Phase-Transfer Catalyzed AlkylationsJ Am Chem Soc2012134291691910.1021/ja211069fSearch in Google Scholar
Soukup O. Benkova M. Dolezal R. et al. The wide-spectrum antimicrobial effect of novel N-alkyl monoquaternary amonium salts and their mixtures; the QSAR study against bakteria. Eur J Med Chem. 2020;206:112584.SoukupOBenkovaMDolezalRThe wide-spectrum antimicrobial effect of novel N-alkyl monoquaternary amonium salts and their mixtures; the QSAR study against bakteriaEur J Med Chem202020611258410.1016/j.ejmech.2020.112584Search in Google Scholar
Thebault P. de Givenchi ET. Levy R. Vandenberghe Y. Guittard F. Géribaldi S. Preparation and antimicrobial behaviour of quaternary ammonium thiol derivatives able to be grafted on metal surfaces. Eur J Med Chem. 2009;44:717–724.ThebaultPde GivenchiETLevyRVandenbergheYGuittardFGéribaldiSPreparation and antimicrobial behaviour of quaternary ammonium thiol derivatives able to be grafted on metal surfacesEur J Med Chem20094471772410.1016/j.ejmech.2008.05.007Search in Google Scholar
Truong TKT. Olivier NVB. Aupoix A. Pegot B. Vo-Thanh G. Chiral Ionic Liquids Derived from (-)-Ephedrine and Carbohydrates: Synthesis, Properties and Applications to Asymmetric Synthesis and Catalysis. Curr Org Synth. 2012; 9(1): 53–64.TruongTKTOlivierNVBAupoixAPegotBVo-ThanhGChiral Ionic Liquids Derived from (-)-Ephedrine and Carbohydrates: Synthesis, Properties and Applications to Asymmetric Synthesis and CatalysisCurr Org Synth201291536410.2174/157017912798889143Search in Google Scholar
Wong Y-L, Hubieki MP, Curfaman CL et al. A Structure–Activity Study of Spermicidal and Anti-HIV Properties of Hydroxylated Cationic Surfactants. Bioorg Med Chem. 2002;10:3599–3608.WongY-LHubiekiMPCurfamanCLA Structure–Activity Study of Spermicidal and Anti-HIV Properties of Hydroxylated Cationic SurfactantsBioorg Med Chem2002103599360810.1016/S0968-0896(02)00245-6Search in Google Scholar
Zhang Y. Zhu W. Liu Y-L. et al. Chemo-Immunotherapeutic Antimalarials Targeting Isoprenoid Biosynthesis. ACS Med Chem Lett. 2013;4:423–427.ZhangYZhuWLiuY-LChemo-Immunotherapeutic Antimalarials Targeting Isoprenoid BiosynthesisACS Med Chem Lett2013442342710.1021/ml4000436363051623610597Search in Google Scholar
Zhi DF. Zhang SB. Qureshi F. et al. Synthesis and biological activity of carbamate-linked cationic lipids for gene delivery in vitro. Bioorg Med Chem Lett. 2012; 22(11): 3837–3841.ZhiDFZhangSBQureshiFSynthesis and biological activity of carbamate-linked cationic lipids for gene delivery in vitroBioorg Med Chem Lett201222113837384110.1016/j.bmcl.2012.01.09722542011Search in Google Scholar