Lista de obras -

1,3,4-Oxadiazole-2(3H)-thione and its analogues: a new class of non-competitive nucleotide pyrophosphatases/phosphodiesterases 1 inhibitors.

artículo científico publicado en 2009

1-[(4'-Chlorophenyl) carbonyl-4-(aryl) thiosemicarbazide derivatives as potent urease inhibitors: Synthesis, in vitro and in silico studies

scientific article published on 23 May 2018

2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors.

artículo científico publicado en 2015

2-Arylquinazolin-4(3H)-ones: A novel class of thymidine phosphorylase inhibitors.

artículo científico publicado en 2015

2-Arylquinazolin-4(3H)-ones: Inhibitory Activities Against Xanthine Oxidase.

artículo científico publicado en 2015

4-Arylamino-6-nitroquinazolines: Synthesis and their activities against neglected disease leishmaniasis.

artículo científico publicado en 2015

5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes.

artículo científico publicado en 2017

A facile and improved synthesis of sildenafil (Viagra) analogs through solid support microwave irradiation possessing tyrosinase inhibitory potential, their conformational analysis and molecular dynamics simulation studies.

artículo científico publicado en 2005

Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers

artículo científico publicado en 2012

Benzothiazole derivatives: novel inhibitors of methylglyoxal mediated glycation of proteins in vitro

artículo científico publicado en 2014

Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.

artículo científico publicado en 2016

Biscoumarin: new class of urease inhibitors; economical synthesis and activity.

Biscoumarin: new class of urease inhibitors; economical synthesis and activity

Carbohydrazones as new class of carbonic anhydrase inhibitors: Synthesis, kinetics, and ligand docking studies.

artículo científico publicado en 2017

Coumarin sulfonates: As potential leads for ROS inhibition

artículo científico publicado en 2016

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.

artículo científico publicado en 2016

Evaluation of bisindole as potent β-glucuronidase inhibitors: synthesis and in silico based studies

artículo científico publicado en 2014

Evaluation of the thiazole Schiff bases as β-glucuronidase inhibitors and their in silico studies

artículo científico publicado en 2014

Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies.

artículo científico publicado en 2017

Identification of potent urease inhibitors via ligand- and structure-based virtual screening and in vitro assays

scientific article published on 17 February 2010

In vitro leishmanicidal activity of 3-substituted isocoumarins: synthesis and structure activity relationship.

artículo científico publicado en 2008

Insulinotropic action of 2, 4-dinitroanilino-benzoic acid through the attenuation of pancreatic beta-cell lesions in diabetic rats.

artículo científico publicado en 2017

Molecular modeling-based antioxidant arylidene barbiturates as urease inhibitors

scientific article published on 07 July 2011

New Hybrid Hydrazinyl Thiazole Substituted Chromones: As Potential α-Amylase Inhibitors and Radical (DPPH & ABTS) Scavengers

artículo científico publicado en 2017

Oxadiazoles and thiadiazoles: novel α-glucosidase inhibitors.

artículo científico publicado en 2014

Oxazolones: new tyrosinase inhibitors; synthesis and their structure-activity relationships

artículo científico publicado en 2006

Oxindole derivatives: synthesis and antiglycation activity

artículo científico publicado en 2013

Phenoxyacetohydrazide Schiff bases: β-glucuronidase inhibitors

artículo científico publicado en 2014

Piperidines: a new class of urease inhibitors

scientific article published on 01 May 2006

Structure-based design, synthesis and biological evaluation of β-glucuronidase inhibitors.

artículo científico publicado en 2014

Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies

artículo científico publicado en 2016

Synthesis and Biological Potential Assessment of 2-Substituted Quinazolin-4(3H)-ones as Inhibitors of Phosphodiesterase-I and Carbonic Anhydrase-II.

artículo científico publicado en 2015

Synthesis and DPPH radical scavenging activity of 5-arylidene-N,N-dimethylbarbiturates

artículo científico publicado en 2011

Synthesis and biological screening of 7-hydroxy-4-methyl-2H-chromen-2-one, 7-hydroxy-4,5-dimethyl-2H-chromen-2-one and their some derivatives.

artículo científico publicado en 2003

Synthesis and in vitro leishmanicidal activity of some hydrazides and their analogues

scientific article published on 01 April 2003

Synthesis and in vitro urease inhibitory activity of N,N'-disubstituted thioureas

artículo científico publicado en 2014

Synthesis and molecular docking studies of potent α-glucosidase inhibitors based on biscoumarin skeleton

scientific article published on 04 May 2014

Synthesis and structure-activity relationship of thiobarbituric acid derivatives as potent inhibitors of urease

artículo científico publicado en 2014

Synthesis and β-glucuronidase inhibitory activity of 2-arylquinazolin-4(3H)-ones.

artículo científico publicado en 2014

Synthesis of benzophenonehydrazone Schiff bases and their in vitro antiglycating activities.

artículo científico publicado en 2013

Synthesis of bis-Schiff bases of isatins and their antiglycation activity.

artículo científico publicado en 2009

Synthesis of diethyl 4-substituted-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates as a new series of inhibitors against yeast α-glucosidase

scientific article published on 11 March 2015

Synthesis of methyl ether analogues of sildenafil (Viagra) possessing tyrosinase inhibitory potential

artículo científico publicado en 2005

Synthesis of triazole Schiff bases: novel inhibitors of nucleotide pyrophosphatase/phosphodiesterase-1.

artículo científico publicado en 2014

Synthesis, antifungal, and phytotoxic effects of some benzopyrone derivatives.

artículo científico publicado en 2004

Synthesis, in vitro [Formula: see text]-glucosidase inhibitory activity, and in silico study of (E)-thiosemicarbazones and (E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivatives

artículo científico publicado en 2018

Synthesis, in vitro urease inhibitory activity, and molecular docking studies of thiourea and urea derivatives

artículo científico publicado en 2018

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives

artículo científico publicado en 2016

Synthesis, in vitro β-glucuronidase inhibitory activity and in silico studies of novel (E)-4-Aryl-2-(2-(pyren-1-ylmethylene)hydrazinyl)thiazoles.

artículo científico publicado en 2016

Synthesis, in vitro β-glucuronidase inhibitory potential and molecular docking studies of quinolines

artículo científico publicado en 2017

Synthesis, structure-activity relationships studies of benzoxazinone derivatives as α-chymotrypsin inhibitors.

artículo científico publicado en 2017

Synthetic indole Mannich bases: Their ability to modulate in vitro cellular immunity.

artículo científico publicado en 2015

Tetraketones: a new class of tyrosinase inhibitors.

artículo científico publicado en 2005

The immunomodulation potential of the synthetic derivatives of benzothiazoles: Implications in immune system disorders through in vitro and in silico studies.

artículo científico publicado en 2015

Thiadiazole derivatives as New Class of β-glucuronidase inhibitors.

artículo científico publicado en 2016

Unsymmetrically disubstituted urea derivatives: a potent class of antiglycating agents.

artículo científico publicado en 2009

β-glucuronidase inhibitory studies on coumarin derivatives.

artículo científico publicado en 2014

Lista de obras de

1,3,4-Oxadiazole-2(3H)-thione and its analogues: a new class of non-competitive nucleotide pyrophosphatases/phosphodiesterases 1 inhibitors.

1-[(4'-Chlorophenyl) carbonyl-4-(aryl) thiosemicarbazide derivatives as potent urease inhibitors: Synthesis, in vitro and in silico studies

2-Arylquinazolin-4(3H)-ones: A new class of α-glucosidase inhibitors.

2-Arylquinazolin-4(3H)-ones: A novel class of thymidine phosphorylase inhibitors.

2-Arylquinazolin-4(3H)-ones: Inhibitory Activities Against Xanthine Oxidase.

4-Arylamino-6-nitroquinazolines: Synthesis and their activities against neglected disease leishmaniasis.

5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes.

A facile and improved synthesis of sildenafil (Viagra) analogs through solid support microwave irradiation possessing tyrosinase inhibitory potential, their conformational analysis and molecular dynamics simulation studies.

Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers

Benzothiazole derivatives: novel inhibitors of methylglyoxal mediated glycation of proteins in vitro

Biology-oriented drug synthesis (BIODS): In vitro β-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.

Biscoumarin: new class of urease inhibitors; economical synthesis and activity.

Carbohydrazones as new class of carbonic anhydrase inhibitors: Synthesis, kinetics, and ligand docking studies.

Coumarin sulfonates: As potential leads for ROS inhibition

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.

Evaluation of bisindole as potent β-glucuronidase inhibitors: synthesis and in silico based studies

Evaluation of the thiazole Schiff bases as β-glucuronidase inhibitors and their in silico studies

Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies.

Identification of potent urease inhibitors via ligand- and structure-based virtual screening and in vitro assays

In vitro leishmanicidal activity of 3-substituted isocoumarins: synthesis and structure activity relationship.

Insulinotropic action of 2, 4-dinitroanilino-benzoic acid through the attenuation of pancreatic beta-cell lesions in diabetic rats.

Molecular modeling-based antioxidant arylidene barbiturates as urease inhibitors

New Hybrid Hydrazinyl Thiazole Substituted Chromones: As Potential α-Amylase Inhibitors and Radical (DPPH & ABTS) Scavengers

Oxadiazoles and thiadiazoles: novel α-glucosidase inhibitors.

Oxazolones: new tyrosinase inhibitors; synthesis and their structure-activity relationships

Oxindole derivatives: synthesis and antiglycation activity

Phenoxyacetohydrazide Schiff bases: β-glucuronidase inhibitors

Piperidines: a new class of urease inhibitors

Structure-based design, synthesis and biological evaluation of β-glucuronidase inhibitors.

Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies

Synthesis and Biological Potential Assessment of 2-Substituted Quinazolin-4(3H)-ones as Inhibitors of Phosphodiesterase-I and Carbonic Anhydrase-II.

Synthesis and DPPH radical scavenging activity of 5-arylidene-N,N-dimethylbarbiturates

Synthesis and biological screening of 7-hydroxy-4-methyl-2H-chromen-2-one, 7-hydroxy-4,5-dimethyl-2H-chromen-2-one and their some derivatives.

Synthesis and in vitro leishmanicidal activity of some hydrazides and their analogues

Synthesis and in vitro urease inhibitory activity of N,N'-disubstituted thioureas

Synthesis and molecular docking studies of potent α-glucosidase inhibitors based on biscoumarin skeleton

Synthesis and structure-activity relationship of thiobarbituric acid derivatives as potent inhibitors of urease

Synthesis and β-glucuronidase inhibitory activity of 2-arylquinazolin-4(3H)-ones.

Synthesis of benzophenonehydrazone Schiff bases and their in vitro antiglycating activities.

Synthesis of bis-Schiff bases of isatins and their antiglycation activity.

Synthesis of diethyl 4-substituted-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates as a new series of inhibitors against yeast α-glucosidase

Synthesis of methyl ether analogues of sildenafil (Viagra) possessing tyrosinase inhibitory potential

Synthesis of triazole Schiff bases: novel inhibitors of nucleotide pyrophosphatase/phosphodiesterase-1.

Synthesis, antifungal, and phytotoxic effects of some benzopyrone derivatives.

Synthesis, in vitro [Formula: see text]-glucosidase inhibitory activity, and in silico study of (E)-thiosemicarbazones and (E)-2-(2-(arylmethylene)hydrazinyl)-4-arylthiazole derivatives

Synthesis, in vitro urease inhibitory activity, and molecular docking studies of thiourea and urea derivatives

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives

Synthesis, in vitro β-glucuronidase inhibitory activity and in silico studies of novel (E)-4-Aryl-2-(2-(pyren-1-ylmethylene)hydrazinyl)thiazoles.

Synthesis, in vitro β-glucuronidase inhibitory potential and molecular docking studies of quinolines

Synthesis, structure-activity relationships studies of benzoxazinone derivatives as α-chymotrypsin inhibitors.

Synthetic indole Mannich bases: Their ability to modulate in vitro cellular immunity.

Tetraketones: a new class of tyrosinase inhibitors.

The immunomodulation potential of the synthetic derivatives of benzothiazoles: Implications in immune system disorders through in vitro and in silico studies.

Thiadiazole derivatives as New Class of β-glucuronidase inhibitors.

Unsymmetrically disubstituted urea derivatives: a potent class of antiglycating agents.

β-glucuronidase inhibitory studies on coumarin derivatives.