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In-vitro biological evaluation of 3,3′,5,5′-tetramethoxy-biphenyl-4,4′-diol and molecular docking studies on trypanothione reductase and Gp63 from Leishmania amazonensis demonstrated anti-leishmania potential

Scientific reports, 2023-04, Vol.13 (1), p.6928-6928, Article 6928

2023

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Novel Organic Salts Based on Mefloquine: Synthesis, Solubility, Permeability, and In Vitro Activity against Mycobacterium tuberculosis

Molecules (Basel, Switzerland), 2022-08, Vol.27 (16), p.5167

2022

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Benzoylthioureas: Design, Synthesis and Antimycobacterial Evaluation

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2020-01, Vol.16 (1), p.93-103

2020

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7-Chloro-4-quinolinyl Hydrazones: A Promising and Potent Class of Antileishmanial Compounds

Chemical biology & drug design, 2013-05, Vol.81 (5), p.658-665

2013

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Computational Strategies Targeting Inhibition of Helicobacter pylori and Cryptococcus neoformans Ureases

Current pharmaceutical design, 2023-01, Vol.29 (10), p.777-792

2023

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Promising Molecular Targets Related to Polyamine Biosynthesis in Drug Discovery against Leishmaniasis

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2023-01, Vol.19 (1), p.2-9

2023

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Anti-Mycobacterial Evaluation of 7-Chloro-4-Aminoquinolines and Hologram Quantitative Structure-Activity Relationship (HQSAR) Modeling of Amino-Imino Tautomers

Pharmaceuticals (Basel, Switzerland), 2017-06, Vol.10 (2), p.52

2017

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Carvacrol and its Semi-synthetic Derivatives as Potential Antibacterial Agents

Revista Virtual de Química, 2023-09, Vol.15 (5), p.984-1009

2023

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In vitro evaluation of antitrypanosomal activity and molecular docking of benzoylthioureas

Parasitology international, 2021-02, Vol.80, p.102225-102225, Article 102225

2021

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Anti-Tuberculosis Evaluation and Conformational Study of N-Acylhydrazones Containing the Thiophene Nucleus

Archiv der Pharmazie (Weinheim), 2014-06, Vol.347 (6), p.432-448

2014

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A new and potent class of quinoline derivatives against cancer

Monatshefte für Chemie, 2015-12, Vol.146 (12), p.2041-2052

2015

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Structures of a co-crystal of tautomers of ( E )-N-7-chloro-4-(2-methoxycinnamolyhydrazinyl)quinoline and a single tautomer of the 4-methoxy analogue

Zeitschrift für Kristallographie. Crystalline materials, 2013-05, Vol.228 (5), p.232-239

2013

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Exploring Urease Inhibition by Coumarin Derivatives through in silico and in vitro Methods

Journal of the Brazilian Chemical Society, 2024, Vol.35 (4)

2024

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Variations in the intermolecular interactions in ( E ) benzaldehyde 7-chloro-1-methyl- 4H-quinolinyl-4-ylidene-hydrazone and seven halo derivatives

Zeitschrift für Kristallographie. Crystalline materials, 2016-04, Vol.231 (4), p.219-235

2016

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Novel Organic Salts Based on Mefloquine: Synthesis, Solubility, Permeability, and In Vitro Activity against IMycobacterium tuberculosis/I

Molecules (Basel, Switzerland), 2022-08, Vol.27 (16)

2022

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In Vitro Anti-Mycobacterial Activity of (E)-N´-(Monosubstituted-benzylidene) Isonicotinohydrazide Derivatives against Isoniazid-Resistant Strains

Infectious disease reports, 2012-02, Vol.4 (1), p.e13-e13

2012

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In Vitro Antimicrobial Screening of Benzoylthioureas: Synthesis, Antibacterial Activity toward Streptococcus agalactiae and Molecular Docking Study

ChemistrySelect (Weinheim), 2022-09, Vol.7 (34), p.n/a

2022

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Structures of three methoxy-substituted benzaldehyde 7-chloro-1-methyl-4H-quinolinyl-4-ylidene-hydrazones: variations in π···π interactions

Zeitschrift für Kristallographie. Crystalline materials, 2015-08, Vol.230 (8), p.519-530

2015

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Amodiaquine analogs. Synthesis and anti-leishmanial activity

Mediterranean journal of chemistry, 2011-09, Vol.1 (3), p.106-113

2011

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Cyclodextrin-encapsulated new drug with promising anti-Trypanosoma cruzi activity

Journal of thermal analysis and calorimetry, 2023-10, Vol.148 (20), p.10821-10834

2023

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In-vitro biological evaluation of 3,3′,5,5′-tetramethoxy-biphenyl-4,4′-diol and molecular docking studies on trypanothione reductase and Gp63 from Leishmania amazonensis demonstrated anti-leishmania potential

Novel Organic Salts Based on Mefloquine: Synthesis, Solubility, Permeability, and In Vitro Activity against Mycobacterium tuberculosis

Benzoylthioureas: Design, Synthesis and Antimycobacterial Evaluation

7-Chloro-4-quinolinyl Hydrazones: A Promising and Potent Class of Antileishmanial Compounds

Computational Strategies Targeting Inhibition of Helicobacter pylori and Cryptococcus neoformans Ureases

Promising Molecular Targets Related to Polyamine Biosynthesis in Drug Discovery against Leishmaniasis

Anti-Mycobacterial Evaluation of 7-Chloro-4-Aminoquinolines and Hologram Quantitative Structure-Activity Relationship (HQSAR) Modeling of Amino-Imino Tautomers

Carvacrol and its Semi-synthetic Derivatives as Potential Antibacterial Agents

In vitro evaluation of antitrypanosomal activity and molecular docking of benzoylthioureas

Anti-Tuberculosis Evaluation and Conformational Study of N-Acylhydrazones Containing the Thiophene Nucleus

A new and potent class of quinoline derivatives against cancer

Structures of a co-crystal of tautomers of ( E )-N-7-chloro-4-(2-methoxycinnamolyhydrazinyl)quinoline and a single tautomer of the 4-methoxy analogue

Exploring Urease Inhibition by Coumarin Derivatives through in silico and in vitro Methods

Variations in the intermolecular interactions in ( E ) benzaldehyde 7-chloro-1-methyl- 4H-quinolinyl-4-ylidene-hydrazone and seven halo derivatives

Novel Organic Salts Based on Mefloquine: Synthesis, Solubility, Permeability, and In Vitro Activity against IMycobacterium tuberculosis/I

In Vitro Anti-Mycobacterial Activity of (E)-N´-(Monosubstituted-benzylidene) Isonicotinohydrazide Derivatives against Isoniazid-Resistant Strains

In Vitro Antimicrobial Screening of Benzoylthioureas: Synthesis, Antibacterial Activity toward Streptococcus agalactiae and Molecular Docking Study

Structures of three methoxy-substituted benzaldehyde 7-chloro-1-methyl-4H-quinolinyl-4-ylidene-hydrazones: variations in π···π interactions

Amodiaquine analogs. Synthesis and anti-leishmanial activity

Cyclodextrin-encapsulated new drug with promising anti-Trypanosoma cruzi activity

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