J. Vinšová

发表

Antimicrobial activity of rhodanine-3-acetic acid derivatives.

M. Krátký, J. Vinšová, J. Stolaříková, 2017, Bioorganic & medicinal chemistry.

Investigating Spectrum of Biological Activity of 4- and 5-Chloro-2-hydroxy-N-[2-(arylamino)-1-alkyl-2-oxoethyl]benzamides

J. Jampílek, K. Kráľová, J. Vinšová, 2011, Molecules.

New derivatives of salicylamides: Preparation and antimicrobial activity against various bacterial species.

J. Jampílek, J. Vinšová, A. Imramovský, 2013, Bioorganic & medicinal chemistry.

Salicylanilide carbamates: Promising antibacterial agents with high in vitro activity against methicillin-resistant Staphylococcus aureus (MRSA).

J. Férriz, Š. Pospíšilová, J. Jampílek, 2015, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Host cell targeting of novel antimycobacterial 4-aminosalicylic acid derivatives with tuftsin carrier peptides.

Gergely Kohut, Á. Babiczky, M. Krátký, 2022, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Substituted pyrazinecarboxamides: synthesis and biological evaluation.

V. Buchta, J. Jampílek, M. Doležal, 2006, Molecules.

Recent advances in drugs and prodrugs design of chitosan.

J. Vinšová, E. Vavříková, J Vinsova, 2008, Current pharmaceutical design.

Antimycobacterial Activity of Salicylanilide Benzenesulfonates

M. Krátký, J. Vinšová, J. Stolaříková, 2012, Molecules.

New amino acid esters of salicylanilides active against MDR-TB and other microbes.

V. Buchta, M. Krátký, J. Vinšová, 2010, European journal of medicinal chemistry.

A new modification of anti-tubercular active molecules.

J. Jampílek, J. Vinšová, A. Imramovský, 2007, Bioorganic & medicinal chemistry.

Synthesis of readily available fluorophenylalanine derivatives and investigation of their biological activity.

L. Navrátilová, M. Krátký, J. Vinšová, 2017, Bioorganic chemistry.

Triclosan and its derivatives as antimycobacterial active agents

M. Krátký, J. Vinšová, Rudolf Vosátka, 2018, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Combating highly resistant emerging pathogen Mycobacterium abscessus and Mycobacterium tuberculosis with novel salicylanilide esters and carbamates.

S. Bősze, M. Krátký, J. Vinšová, 2015, European journal of medicinal chemistry.

Phenolic N-monosubstituted carbamates: Antitubercular and toxicity evaluation of multi-targeting compounds.

E. Novotná, S. Bősze, M. Krátký, 2019, European journal of medicinal chemistry.

Novel derivatives of nitro-substituted salicylic acids: Synthesis, antimicrobial activity and cytotoxicity.

G. Besra, P. Pávek, M. Krátký, 2015, Bioorganic & medicinal chemistry.

Synthesis and in vitro biological evaluation of 2-(phenylcarbamoyl)phenyl 4-substituted benzoates.

S. Bősze, M. Krátký, J. Vinšová, 2015, Bioorganic & medicinal chemistry.

Synthesis and biological activity of new salicylanilide N,N-disubstituted carbamates and thiocarbamates.

E. Novotná, M. Krátký, J. Vinšová, 2014, Bioorganic & medicinal chemistry.

In Vitro Bactericidal Activity of 4- and 5-Chloro-2-hydroxy-N-[1-oxo-1-(phenylamino)alkan-2-yl]benzamides against MRSA

Š. Pospíšilová, J. Jampílek, J. Vinšová, 2015, BioMed research international.

Antioxidant Polymers by Chitosan Modification

J. Vinšová, Eva Vavřková, 2012 .

New lipophilic isoniazid derivatives and their 1,3,4-oxadiazole analogues: Synthesis, antimycobacterial activity and investigation of their mechanism of action.

Jana Korduláková, M. Krátký, J. Vinšová, 2018, European journal of medicinal chemistry.

Synthesis and antimicrobial activity of sulphamethoxazole-based ureas and imidazolidine-2,4,5-triones

V. Buchta, M. Krátký, J. Vinšová, 2015, Chemical Papers.

Hydrazones of 4-(Trifluoromethyl)benzohydrazide as New Inhibitors of Acetyl- and Butyrylcholinesterase

Q. A. Vu, M. Krátký, J. Vinšová, 2021, Molecules.

Salicylanilide esterification : unexpected formation of novel seven-membered rings

J. Férriz, M. Doležal, J. Vinšová, 2006 .

Antibacterial Activity of Salicylanilide 4-(Trifluoromethyl)benzoates

E. Novotná, M. Krátký, J. Vinšová, 2013, Molecules.

Synthesis and in vitro antimycobacterial activity of 2-methoxybenzanilides and their thioxo analogues.

E. Novotná, J. Vinšová, J. Stolaříková, 2012, European journal of medicinal chemistry.

Salicylanilide derivatives block Mycobacterium tuberculosis through inhibition of isocitrate lyase and methionine aminopeptidase.

Jun O. Liu, E. Novotná, M. Krátký, 2012, Tuberculosis.

5-Aryl-1,3,4-oxadiazol-2-amines Decorated with Long Alkyl and Their Analogues: Synthesis, Acetyl- and Butyrylcholinesterase Inhibition and Docking Study

M. Krátký, J. Vinšová, Šárka Štěpánková, 2022, Pharmaceuticals.

2-Hydroxy-N-phenylbenzamides and Their Esters Inhibit Acetylcholinesterase and Butyrylcholinesterase

M. Krátký, J. Vinšová, Šárka Štěpánková, 2019, Biomolecules.

Substituted N-phenylitaconamides as inhibitors of mycobacteria and mycobacterial isocitrate lyase.

E. Novotná, M. Krátký, J. Vinšová, 2022, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Synthesis and in vitro antimycobacterial and isocitrate lyase inhibition properties of novel 2-methoxy-2'-hydroxybenzanilides, their thioxo analogues and benzoxazoles.

E. Novotná, J. Vinšová, J. Stolaříková, 2012, European journal of medicinal chemistry.

Antimicrobial activity of sulfonamides containing 5-chloro-2-hydroxybenzaldehyde and 5-chloro-2-hydroxybenzoic acid scaffold.

V. Buchta, M. Krátký, J. Vinšová, 2012, European journal of medicinal chemistry.

Highly Lipophilic Benzoxazoles with Potential Antibacterial Activity

V. Buchta, J. Vinšová, V. Horák, 2004, Molecules.

Optimizing the structure of (salicylideneamino)benzoic acids: Towards selective antifungal and anti-staphylococcal agents.

K. Konečná, M. Krátký, J. Vinšová, 2021, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Spectroscopic investigations and computational study of 2-[acetyl(4-bromophenyl)carbamoyl]-4-chlorophenyl acetate

Y. Mary, C. Alsenoy, J. Vinšová, 2010 .

FT‐IR, FT‐Raman and DFT calculations of the salicylanilide derivate 4‐chloro‐2‐(4‐bromophenylcarbamoyl)phenyl acetate

C. Alsenoy, V. Madhavan, J. Vinšová, 2009 .

Spectroscopic investigations, concentration dependent SERS, and molecular docking studies of a hydroxybenzylidene derivative

Y. Mary, Y. Mary, Veena S. Kumar, 2021, Journal of biomolecular structure & dynamics.

SERS spectroscopy for the therapeutic N-butyl-2-isonicotinoylhydrazine-1-carboxamide in silver nanocolloids at different concentrations: Experimental and DFT investigations

Y. Mary, Y. Mary, J. S. Al-Otaibi, 2023, Journal of Molecular Structure.

Novel Cholinesterase Inhibitors Based on O-Aromatic N,N-Disubstituted Carbamates and Thiocarbamates

M. Krátký, J. Vinšová, Šárka Štěpánková, 2016, Molecules.

New fluorine-containing hydrazones active against MDR-tuberculosis.

S. Bősze, K. Vávrová, J. Vinšová, 2011, European journal of medicinal chemistry.

Synthesis and antimicrobial evaluation of new 2-substituted 5,7-di-tert-butylbenzoxazoles.

K. Cermakova, M. Ceckova, F. Staud, 2006, Bioorganic & medicinal chemistry.

Concentration and solvent dependent SERS, DFT, MD simulations and molecular docking studies of a thioxothiazolidine derivative with antimicrobial properties

Y. Mary, Y. Mary, M. Krátký, 2021 .

N-Alkyl-2-[4-(trifluoromethyl)benzoyl]hydrazine-1-carboxamides and Their Analogues: Synthesis and Multitarget Biological Activity

S. Bősze, M. Krátký, J. Vinšová, 2020, Molecules.

Synthesis and biological evolution of hydrazones derived from 4-(trifluoromethyl)benzohydrazide.

S. Bősze, M. Krátký, J. Vinšová, 2017, Bioorganic & medicinal chemistry letters.

N-Substituted 2-Isonicotinoylhydrazinecarboxamides — New Antimycobacterial Active Molecules

M. Krátký, J. Vinšová, J. Stolaříková, 2014, Molecules.

Recent Advances on Isoniazide Derivatives

J. Jampílek, M. Doležal, J. Vinšová, 2008 .

DFT, SERS-concentration and solvent dependent and docking studies of a bioactive benzenesulfonamide derivative

M. Krátký, J. Vinšová, Y. Sheena Mary, 2021 .

Synthesis and in vitro evaluation of novel rhodanine derivatives as potential cholinesterase inhibitors.

M. Krátký, J. Vinšová, Šárka Štěpánková, 2016 .

Sulfadiazine Salicylaldehyde-Based Schiff Bases: Synthesis, Antimicrobial Activity and Cytotoxicity

K. Konečná, M. Krátký, J. Vinšová, 2017, Molecules.

Antimycobacterial derivatives of tetrazole

A. Hrabálek, J. Vinšová, K. Waisser, 1991 .

Synthesis and Antimycobacterial and Photosynthesis-Inhibiting Evaluation of 2-[(E)-2-Substituted-ethenyl]-1,3-benzoxazoles

J. Jampílek, K. Kráľová, J. Vinšová, 2014, TheScientificWorldJournal.

Preparation, in vitro evaluation and molecular modelling of pyridinium-quinolinium/isoquinolinium non-symmetrical bisquaternary cholinesterase inhibitors.

K. Kuča, D. Jun, K. Musílek, 2013, Bioorganic & medicinal chemistry letters.

In vitro antibacterial and antifungal activity of salicylanilide pyrazine-2-carboxylates.

V. Buchta, M. Krátký, J. Vinšová, 2012, Medicinal chemistry (Shariqah (United Arab Emirates)).

New series of isoniazid hydrazones linked with electron-withdrawing substituents.

S. Bősze, J. Vinšová, J. Stolaříková, 2011, European journal of medicinal chemistry.

FT-IR, FT-Raman and DFT calculations of 4-chloro-2-(3,4-dichlorophenylcarbamoyl)phenyl acetate.

V. Madhavan, J. Vinšová, C. Y. Panicker, 2009, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

Antiviral activity of substituted salicylanilides--a review.

M. Krátký, J. Vinšová, 2011, Mini reviews in medicinal chemistry.

4-Aminobenzoic Acid Derivatives: Converting Folate Precursor to Antimicrobial and Cytotoxic Agents

K. Konečná, M. Krátký, J. Vinšová, 2019, Biomolecules.

FT-IR, FT-Raman, and computational calculations of 4-chloro-2-(3-chlorophenyl carbamoyl)phenyl acetate

Y. Mary, Y. Mary, C. Alsenoy, 2009 .

DFT, TD-DFT and SERS analysis of a bioactive benzohydrazide’s adsorption in silver hydrosols at various concentrations

Y. Mary, Y. Mary, J. S. Al-Otaibi, 2023, Journal of Molecular Liquids.

Salicylanilide carbamates: antitubercular agents active against multidrug-resistant Mycobacterium tuberculosis strains.

J. Férriz, K. Vávrová, J. Vinšová, 2010, Bioorganic & medicinal chemistry.

Vibrational spectroscopic studies and computational calculations of 5-chloro-2-(3-chlorophenylcarbamoyl)phenylacetate.

Y. Mary, C. Van Alsenoy, V. Madhavan, 2012, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

Antifungal Activity of Salicylanilides and Their Esters with 4-(Trifluoromethyl)benzoic Acid

M. Krátký, J. Vinšová, 2012, Molecules.

Photosynthesis-Inhibiting efficiency of 4-chloro-2-(chlorophenylcarbamoyl)phenyl alkylcarbamates.

J. Férriz, J. Jampílek, K. Kráľová, 2011, Bioorganic & medicinal chemistry letters.

Salicylanilide esters of N-protected amino acids as novel antimicrobial agents.

J. Férriz, V. Buchta, J. Jampílek, 2009, Bioorganic & medicinal chemistry letters.

CHITOSAN UTILIZATION IN ANTITUBERCULAR PRODRUGS DEVELOPMENT

V. Briedis, A. Savickas, L. Ivanauskas, 2010 .

Morpholine-2,5-diones - Their Preparation and Exploitation

J. Vinšová, 2001 .

Effect of alaptide, its analogues and oxiracetam on memory for an elevated plus-maze in mice.

J. Vinšová, Z. Hliňák, E. Kasafírek, 1996, European journal of pharmacology.

An unprecedented rearrangement of salicylanilide derivatives: imidazolinone intermediate formation

J. Férriz, A. Růžička, A. Lyčka, 2010 .

New antituberculotics originated from salicylanilides with promising in vitro activity against atypical mycobacterial strains.

J. Férriz, R. Doležal, J. Jampílek, 2009, Bioorganic & medicinal chemistry.

Cytotoxicity decreasing effect and antimycobacterial activity of chitosan conjugated with antituberculotic drugs

J. Vinšová, J. Stolaříková, J. Mandíková, 2011 .

Acetylcholinesterase-Inhibiting Activity of Salicylanilide N-Alkylcarbamates and Their Molecular Docking

J. Jampílek, J. Vinšová, A. Imramovský, 2012, Molecules.

Antimycobacterial activity of quaternary pyridinium salts and pyridinium N-oxides--review.

M. Krátký, J. Vinšová, 2012, Current pharmaceutical design.

Salicylanilide diethyl phosphates as cholinesterases inhibitors.

M. Krátký, J. Vinšová, Šárka Štěpánková, 2015, Bioorganic chemistry.

Salicylanilide diethyl phosphates: synthesis, antimicrobial activity and cytotoxicity.

V. Buchta, M. Krátký, J. Vinšová, 2014, Bioorganic & medicinal chemistry.

Salicylanilide acetates: synthesis and antibacterial evaluation.

V. Buchta, M. Ceckova, F. Staud, 2007, Molecules.

Synthesis, Biological Evaluation, and In Silico Modeling of N-Substituted Quinoxaline-2-Carboxamides

K. Konečná, M. Doležal, J. Vinšová, 2021, Pharmaceuticals.

Design and synthesis of 2-(2-isonicotinoylhydrazineylidene)propanamides as InhA inhibitors with high antitubercular activity.

S. Bősze, Jana Korduláková, M. Krátký, 2021, European journal of medicinal chemistry.

5-Alkylamino-N-phenylpyrazine-2-carboxamides: Design, Preparation, and Antimycobacterial Evaluation

K. Konečná, M. Doležal, J. Vinšová, 2020, Molecules.

Design, synthesis and antimycobacterial activity of hybrid molecules combining pyrazinamide with a 4-phenylthiazol-2-amine scaffold.

L. Navrátilová, M. Doležal, J. Vinšová, 2018, MedChemComm.

Salicylanilide pyrazinoates inhibit in vitro multidrug-resistant Mycobacterium tuberculosis strains, atypical mycobacteria and isocitrate lyase.

E. Novotná, M. Krátký, J. Vinšová, 2014, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Design and Synthesis of Highly Active Antimycobacterial Mutual Esters of 2-(2-Isonicotinoylhydrazineylidene)propanoic Acid

Jana Korduláková, M. Krátký, J. Vinšová, 2021, Pharmaceuticals.

Salicylanilide ester prodrugs as potential antimicrobial agents--a review.

M. Krátký, J. Vinšová, 2011, Current pharmaceutical design.

Synthesis and antimycobacterial evaluation of substituted pyrazinecarboxamides.

V. Buchta, J. Jampílek, M. Doležal, 2008, European journal of medicinal chemistry.

Synthesis and Hydrophobic Properties of Benzoxazoles

J. Jampílek, J. Vinšová, J. Dohnal, 2005 .

In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates.

S. Bősze, M. Krátký, J. Vinšová, 2017, European journal of medicinal chemistry.

Novel salicylanilides from 4,5-dihalogenated salicylic acids: Synthesis, antimicrobial activity and cytotoxicity.

L. Navrátilová, M. Krátký, J. Vinšová, 2017, Bioorganic & medicinal chemistry.

Advances in mycobacterial isocitrate lyase targeting and inhibitors.

M. Krátký, J. Vinšová, 2012, Current medicinal chemistry.

Antimycobacterial Assessment of Salicylanilide Benzoates including Multidrug-Resistant Tuberculosis Strains

M. Krátký, J. Vinšová, J. Stolaříková, 2012, Molecules.

Sulphur-Containing Heterocycles as Antimycobacterial Agents: Recent Advances in Thiophene and Thiadiazole Derivatives.

M. Krátký, J. Vinšová, 2016, Current topics in medicinal chemistry.

In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates

V. Buchta, M. Krátký, J. Vinšová, 2012, TheScientificWorldJournal.

Sulfonamide-salicylaldehyde imines active against methicillin- and trimethoprim/sulfonamide-resistant Staphylococci.

K. Konečná, M. Krátký, J. Vinšová, 2021, Future medicinal chemistry.

Investigation of salicylanilide and 4-chlorophenol-based N-monosubstituted carbamates as potential inhibitors of acetyl- and butyrylcholinesterase.

M. Krátký, J. Vinšová, Šárka Štěpánková, 2018, Bioorganic chemistry.

In vitro activity of salicylamide derivatives against vancomycin-resistant enterococci.

Š. Pospíšilová, J. Jampílek, J. Vinšová, 2018, Bioorganic & medicinal chemistry letters.

Concentration dependent SERS, DFT and molecular docking studies of a ureido derivative with antitubercular properties.

Y. Mary, Y. Mary, M. Krátký, 2020, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

5,7-Di-tert-butyl-2-(2-pyridyl)benzo[d]oxazole

J. Marek, J. Vinšová, J. Vančo, 2007 .

Novel Aminoguanidine Hydrazone Analogues: From Potential Antimicrobial Agents to Potent Cholinesterase Inhibitors

K. Konečná, M. Krátký, J. Vinšová, 2021, Pharmaceuticals.

Salicylanilide N-monosubstituted carbamates: Synthesis and in vitro antimicrobial activity.

M. Krátký, J. Vinšová, 2016, Bioorganic & medicinal chemistry.

SERS spectra of a bioactive carboximidamide derivative at different concentrations: Experimental and DFT investigations

Y. Mary, Y. Mary, J. S. Al-Otaibi, 2022, Journal of Molecular Structure.

Concentration dependent SERS study of a bioactive methylsulfonyl derivative

Y. Mary, Y. Mary, J. S. Al-Otaibi, 2022, Journal of Molecular Liquids.

The concentration dependent SERS studies of a bioactive 4-chlorobenzylidene derivative: Experimental and DFT investigations

M. Krátký, J. Vinšová, Y. Sheena Mary, 2023, Journal of Molecular Liquids.

DFT, molecular docking and SERS (concentration and solvent dependant) investigations of a methylisoxazole derivative with potential antimicrobial activity

M. Krátký, J. Vinšová, Y. Sheena Mary, 2021 .

Spectroscopic investigations, concentration dependent SERS, and molecular docking studies of a benzoic acid derivative.

Y. Mary, Y. Mary, M. Krátký, 2020, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

N-[3,5-Bis(trifluoromethyl)phenyl]-5-bromo-2-hydroxybenzamide Analogues: Novel Acetyl- and Butyrylcholinesterase Inhibitors.

M. Krátký, J. Vinšová, Šárka Štěpánková, 2020, Current topics in medicinal chemistry.

Novel Sulfamethoxazole Ureas and Oxalamide as Potential Antimycobacterial Agents

M. Krátký, J. Vinšová, J. Stolaříková, 2017, Molecules.

Improving the antimicrobial activity of old antibacterial drug mafenide: Schiff bases and their bioactivity targeting resistant pathogens.

K. Konečná, M. Krátký, J. Vinšová, 2023, Future medicinal chemistry.

Vibrational spectroscopic investigations and computational study of 5-chloro-2-[4-(trifluoromethyl)phenylcarbamoyl]phenyl acetate.

C. Van Alsenoy, J. Vinšová, C. Y. Panicker, 2013, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

Conformations, equilibrium thermodynamics and rotational barriers of secondary thiobenzanilides

J. Vinšová, J. Kuneš, V. Římal, 2016 .

Concentration dependent SERS profile of p-tolyl 2-acetamido-3-(4-fluorophenyl)propanoate (AFP) in silver colloidal nanohydrosols: Experimental and DFT investigations

Y. Mary, Y. Mary, J. S. Al-Otaibi, 2023, Journal of Molecular Structure.

TD-DFT, DFT, docking, MD simulations, and concentration-dependent SERS investigations of a bioactive trifluoromethyl derivative having human acetylcholinesterase and butyrylcholinesterase in silver colloids

Y. Mary, Y. Mary, T. Mahmood, 2023, Journal of Molecular Modeling.

Prodrug design of phenolic drugs.

J. Férriz, J. Vinšová, 2010, Current pharmaceutical design.

Novel propargylamine-based inhibitors of cholinesterases and monoamine oxidases: Synthesis, biological evaluation and docking study.

Q. A. Vu, M. Ambroz, S. Alcaro, 2021, Bioorganic chemistry.

Novel Inhibitors of Acetyl- and Butyrylcholinesterase Derived from Benzohydrazides: Synthesis, Evaluation and Docking Study

M. Krátký, J. Vinšová, Šárka Štěpánková, 2023, Pharmaceuticals.

In vitro biological evaluation of new antimycobacterial salicylanilide-tuftsin conjugates.

S. Bősze, M. Krátký, J. Vinšová, 2017, European journal of medicinal chemistry.

Iodinated 1,2-diacylhydrazines, benzohydrazide-hydrazones and their analogues as dual antimicrobial and cytotoxic agents.

K. Konečná, M. Krátký, J. Vinšová, 2021, Bioorganic & medicinal chemistry.

New derivatives of salicylamides: Preparation and antimicrobial activity against various bacterial species.

J. Jampílek, J. Vinšová, A. Imramovský, 2013, Bioorganic & medicinal chemistry.

Salicylanilide esters of N-protected amino acids as novel antimicrobial agents.

J. Férriz, V. Buchta, J. Jampílek, 2009, Bioorganic & medicinal chemistry letters.

Salicylanilide Diethyl Phosphates as Potential Inhibitors of Some Mycobacterial Enzymes

P. Yogeeswari, D. Sriram, E. Novotná, 2014, TheScientificWorldJournal.

New Salicylanilide Derivatives and Their Peptide Conjugates as Anticancer Compounds: Synthesis, Characterization, and In Vitro Effect on Glioblastoma

S. Bősze, M. Krátký, J. Vinšová, 2024, ACS omega.

Cellular Internalization and Inhibition Capacity of New Anti-Glioma Peptide Conjugates: Physicochemical Characterization and Evaluation on Various Monolayer- and 3D-Spheroid-Based in Vitro Platforms.

S. Bősze, É. Kiss, L. Cervenak, 2021, Journal of medicinal chemistry.

Hidden potential of hydrazinecarboxamides (semicarbazides) as potential antimicrobial agents: A review.

M. Krátký, J. Vinšová, N. Houngbedji, 2024, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Hydrazinecarboxamides: Comprehensive review of their anticancer, anticonvulsive, anti-inflammatory, enzyme inhibition, antioxidant and other activities.

M. Krátký, J. Vinšová, N. Houngbedji, 2024, European journal of medicinal chemistry.