Lista de obras - Muhammad Taha - Dominio Público Uruguay

(E)-2,4-Dimethyl-N'-(2-methyl-benzyl-idene)benzohydrazide.

artículo científico publicado en 2013

(E)-2-Meth-oxy-N'-(2,4,6-trihy-droxy-benzyl-idene)benzohydrazide.

artículo científico publicado en 2013

(E)-3-Chloro-N'-(2-fluoro-benzyl-idene)thio-phene-2-carbohydrazide.

artículo científico publicado en 2014

(E)-4-Meth-oxy-N'-(3,4,5-trihy-droxy-benzyl-idene)benzohydrazide methanol monosolvate.

artículo científico publicado en 2012

(E)-4-Meth-oxy-N'-[(pyridin-4-yl)methyl-idene]benzohydrazide monohydrate

artículo científico publicado en 2012

(E)-N'-(3,4-Dihy-droxy-benzyl-idene)-2,4-dimethyl-benzohydrazide monohydrate.

artículo científico publicado en 2013

(E)-N'-(3,4-Dimeth-oxy-benzyl-idene)-4-meth-oxy-benzohydrazide.

artículo científico publicado en 2012

(E)-N'-(4-Chloro-benzyl-idene)-2-meth-oxy-benzohydrazide.

artículo científico publicado en 2013

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

2,5-Disubstituted thiadiazoles as potent β-glucuronidase inhibitors; Synthesis, in vitro and in silico studies

artículo científico publicado en 2019

2-Aryl benzimidazoles: Synthesis, In vitro α-amylase inhibitory activity, and molecular docking study.

artículo científico publicado en 2018

2-{[2-(2-Hy-droxy-5-meth-oxy-benzyl-idene)hydrazin-1-yl-idene]meth-yl}-4-meth-oxy-phenol.

artículo científico publicado en 2014

3,4-Dimethoxybenzohydrazide derivatives as antiulcer: Molecular modeling and density functional studies.

artículo científico publicado en 2017

3-[2-(Triphenyl-phosphanyl-idene)acet-yl]-2H-chromen-2-one.

artículo científico publicado en 2013

5-Acetyl-6-methyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones: As potent urease inhibitors; synthesis, in vitro screening, and molecular modeling study

artículo científico publicado en 2017

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

artículo científico publicado en 2017

6-Nitrobenzimidazole derivatives: potential phosphodiesterase inhibitors: synthesis and structure-activity relationship

artículo científico publicado en 2011

Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers

artículo científico publicado en 2012

An expeditious synthetic approach towards the synthesis of Bis-Schiff bases (aldazines) using ultrasound.

artículo científico publicado en 2013

Antibiofilm potential of synthetic 2-amino-5-chlorobenzophenone Schiff bases and its confirmation through fluorescence microscopy.

artículo científico publicado en 2017

Antioxidant properties of phenolic Schiff bases: structure-activity relationship and mechanism of action.

artículo científico publicado en 2013

Atenolol thiourea hybrid as potent urease inhibitors: Design, biology-oriented drug synthesis, inhibitory activity screening, and molecular docking studies

artículo científico publicado en 2019

Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies.

artículo científico publicado en 2015

Benzimidazole derivatives protect against cytokine-induced apoptosis in pancreatic β-Cells

artículo científico publicado en 2015

Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies.

artículo científico publicado en 2017

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

Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Chalcones and bis-chalcones: As potential α-amylase inhibitors; synthesis, in vitro screening, and molecular modelling studies

artículo científico publicado en 2018

Coumarin sulfonates: As potential leads for ROS inhibition

artículo científico publicado en 2016

Crystal structure of (E)-N'-benzyl-idene-2-meth-oxy-benzohydrazide

artículo científico publicado en 2014

Design, synthesis, in vitro evaluation, molecular docking and ADME properties studies of hybrid bis-coumarin with thiadiazole as a new inhibitor of Urease

scientific article published on 30 August 2019

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.

artículo científico publicado en 2016

Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions.

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies

scientific article published on 24 March 2016

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

artículo científico publicado en 2017

In silico binding analysis and SAR elucidations of newly designed benzopyrazine analogs as potent inhibitors of thymidine phosphorylase.

artículo científico publicado en 2016

Indole bearing thiadiazole analogs: synthesis, β-glucuronidase inhibition and molecular docking study

scientific article published on 04 February 2019

Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies

scientific article published on 18 April 2015

Leishmanicidal potential of N-substituted morpholine derivatives: synthesis and structure-activity relationships

artículo científico publicado en 2009

Methyl (E)-3,5-dimeth-oxy-2-{[2-(4-meth-oxy-benzo-yl)hydrazin-1-yl-idene]meth-yl}benzoate.

artículo científico publicado en 2012

Molecular hybridization conceded exceptionally potent quinolinyl-oxadiazole hybrids through phenyl linked thiosemicarbazide antileishmanial scaffolds: In silico validation and SAR studies

artículo científico publicado en 2017

N'-[(E)-2,3-Dihy-droxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

artículo científico publicado en 2012

N'-[(E)-2-Hy-droxy-5-meth-oxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

artículo científico publicado en 2012

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

artículo científico publicado en 2017

New triazinoindole bearing thiazole/oxazole analogues: Synthesis, α-amylase inhibitory potential and molecular docking study

scientific article published on 17 September 2019

Novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone: a new class of β-glucuronidase inhibitors and in silico studies.

artículo científico publicado en 2015

Oxindole based oxadiazole hybrid analogs: Novel α-glucosidase inhibitors

artículo científico publicado en 2017

Oxindole derivatives: synthesis and antiglycation activity

artículo científico publicado en 2013

Phenoxyacetohydrazide Schiff bases: β-glucuronidase inhibitors

artículo científico publicado en 2014

Rational design of bis-indolylmethane-oxadiazole hybrids as inhibitors of thymidine phosphorylase

artículo científico publicado en 2018

Schiff bases of tryptamine as potent inhibitors of nucleoside triphosphate diphosphohydrolases (NTPDases): Structure-activity relationship

artículo científico publicado en 2018

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

artículo científico publicado en 2011

Synthesis and biological evaluation of indole derivatives as α-amylase inhibitor

artículo científico publicado en 2017

Synthesis and biological evaluation of novel N-arylidenequinoline-3-carbohydrazides as potent β-glucuronidase inhibitors.

artículo científico publicado en 2016

Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As β-glucuronidase inhibitors.

artículo científico publicado en 2017

Synthesis and in vitro Leishmanicidal Activity of Disulfide Derivatives ⬇️

artículo científico publicado el 1 de noviembre de 2011

Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases

artículo científico publicado en 2016

Synthesis and in vitro study of benzofuran hydrazone derivatives as novel alpha-amylase inhibitor

artículo científico publicado en 2017

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 molecular docking study of piperazine derivatives as potent inhibitor of thymidine phosphorylase

artículo científico publicado en 2018

Synthesis and molecular docking study of piperazine derivatives as potent urease inhibitors

artículo científico publicado en 2018

Synthesis and molecular modelling studies of phenyl linked oxadiazole-phenylhydrazone hybrids as potent antileishmanial agents.

artículo científico publicado en 2016

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

artículo científico publicado en 2014

Synthesis and study of the α-amylase inhibitory potential of thiadiazole quinoline derivatives

artículo científico publicado en 2017

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

artículo científico publicado en 2014

Synthesis of 2,4,6-Trichlorophenyl Hydrazones and their Inhibitory Potential Against Glycation of Protein ⬇️

artículo científico publicado el 1 de noviembre de 2011

Synthesis of 2-acylated and sulfonated 4-hydroxycoumarins: In vitro urease inhibition and molecular docking studies

scientific article published on 26 April 2016

Synthesis of 2-methoxybenzoylhydrazone and evaluation of their antileishmanial activity

artículo científico publicado en 2013

Synthesis of 3,4,5-trihydroxybenzohydrazone and evaluation of their urease inhibition potential

Synthesis of 4-methoxybenzoylhydrazones and evaluation of their antiglycation activity

artículo científico publicado en 2014

Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents

artículo científico publicado en 2015

Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies

artículo científico publicado en 2016

Synthesis of Benzimidazole-Based Analogs as Anti Alzheimer's Disease Compounds and Their Molecular Docking Studies

artículo científico publicado en 2020

Synthesis of Bis-indolylmethane sulfonohydrazides derivatives as potent α-Glucosidase inhibitors

artículo científico publicado en 2018

Synthesis of Chromen-4-One-Oxadiazole Substituted Analogs as Potent -Glucuronidase Inhibitors

artículo científico publicado en 2019

Synthesis of Novel Triazinoindole-Based Thiourea Hybrid: A Study on α-Glucosidase Inhibitors and Their Molecular Docking

scientific article published on 23 October 2019

Synthesis of Thymidine Phosphorylase Inhibitor Based on Quinoxaline Derivatives and Their Molecular Docking Study

artículo científico publicado en 2019

Synthesis of alpha amylase inhibitors based on privileged indole scaffold

artículo científico publicado en 2017

Synthesis of benzimidazole derivatives as potent β-glucuronidase inhibitors

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Synthesis of benzothiazole derivatives as a potent α-glucosidase inhibitor

artículo científico publicado en 2018

Synthesis of benzotriazoles derivatives and their dual potential as α-amylase and α-glucosidase inhibitors in vitro: Structure-activity relationship, molecular docking, and kinetic studies

artículo científico publicado en 2019

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

artículo científico publicado en 2009

Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies

artículo científico publicado en 2017

Synthesis of indole analogs as potent β-glucuronidase inhibitors.

artículo científico publicado en 2017

Synthesis of new arylhydrazide bearing Schiff bases/thiazolidinone: α-Amylase, urease activities and their molecular docking studies

artículo científico publicado en 2019

Synthesis of new indazole based dual inhibitors of α-glucosidase and α-amylase enzymes, their in vitro, in silico and kinetics studies

scientific article published on 23 August 2019

Synthesis of new isoquinoline-base-oxadiazole derivatives as potent inhibitors of thymidine phosphorylase and molecular docking study

artículo científico publicado en 2019

Synthesis of new oxadiazole derivatives as α-glucosidase inhibitors

scientific article published on 02 July 2015

Synthesis of novel benzohydrazone-oxadiazole hybrids as β-glucuronidase inhibitors and molecular modeling studies

scientific article published on 26 October 2015

Synthesis of novel bisindolylmethane Schiff bases and their antibacterial activity.

artículo científico publicado en 2014

Synthesis of novel bisindolylmethanes: New carbonic anhydrase II inhibitors, docking, and 3D pharmacophore studies.

artículo científico publicado en 2016

Synthesis of novel derivatives of 4-methylbenzimidazole and evaluation of their biological activities.

artículo científico publicado en 2014

Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies

artículo científico publicado en 2015

Synthesis of novel disulfide and sulfone hybrid scaffolds as potent β-glucuronidase inhibitor.

artículo científico publicado en 2016

Synthesis of novel flavone hydrazones: in-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies.

artículo científico publicado en 2015

Synthesis of novel inhibitors of α-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies

artículo científico publicado en 2015

Synthesis of novel inhibitors of β-glucuronidase based on benzothiazole skeleton and study of their binding affinity by molecular docking

artículo científico publicado en 2011

Synthesis of novel quinoline-based thiadiazole, evaluation of their antileishmanial potential and molecular docking studies

scientific article published on 21 December 2018

Synthesis of oxadiazole-coupled-thiadiazole derivatives as a potent β-glucuronidase inhibitors and their molecular docking study

scientific article published on 04 June 2019

Synthesis of piperazine sulfonamide analogs as diabetic-II inhibitors and their molecular docking study

artículo científico publicado en 2017

Synthesis of potent urease inhibitors based on disulfide scaffold and their molecular docking studies.

artículo científico publicado en 2015

Synthesis of quinoline derivatives as diabetic II inhibitors and molecular docking studies

scientific article published on 20 July 2019

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

artículo científico publicado en 2014

Synthesis, Molecular Docking and β-Glucuronidase Inhibitory Potential of Indole Base Oxadiazole Derivatives ⬇️

artículo científico publicado en 2019

Synthesis, SAR elucidations and molecular docking study of newly designed isatin based oxadiazole analogs as potent inhibitors of thymidine phosphorylase

scientific article published on 17 May 2018

Synthesis, anti-leishmanial and molecular docking study of bis-indole derivatives

scientific article published on 06 August 2019

Synthesis, biological evaluation, and docking studies of novel thiourea derivatives of bisindolylmethane as carbonic anhydrase II inhibitor

artículo científico publicado en 2015

Synthesis, crystal structure, DFT studies and evaluation of the antioxidant activity of 3,4-dimethoxybenzenamine schiff bases.

artículo científico publicado en 2014

Synthesis, evaluation of antioxidant activity and crystal structure of 2,4-dimethylbenzoylhydrazones.

artículo científico publicado en 2013

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 alpha-glucosidase inhibitory potential of benzimidazole bearing bis-Schiff bases and their molecular docking study

artículo científico publicado en 2019

Synthesis, in vitro evaluation and molecular docking studies of biscoumarin thiourea as a new inhibitor of α-glucosidases

artículo científico publicado en 2015

Synthesis, in vitro evaluation and molecular docking studies of thiazole derivatives as new inhibitors of α-glucosidase.

artículo científico publicado en 2015

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

artículo científico publicado en 2018

Synthesis, in vitro urease inhibitory potential and molecular docking study of Benzimidazole analogues

artículo científico publicado en 2019

Synthesis, in vitro α-amylase inhibitory, and radicals (DPPH & ABTS) scavenging potentials of new N-sulfonohydrazide substituted indazoles

scientific article published on 31 October 2019

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

artículo científico publicado en 2016

Synthesis, in vitro α-glucosidase inhibitory potential and molecular docking study of thiadiazole analogs

artículo científico publicado en 2018

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, molecular docking and α-glucosidase inhibition of 5-aryl-2-(6'-nitrobenzofuran-2'-yl)-1,3,4-oxadiazoles

artículo científico publicado en 2016

Synthesis, molecular docking studies of hybrid benzimidazole as α-glucosidase inhibitor

artículo científico publicado en 2016

Synthesis, molecular docking study and in vitro thymidine phosphorylase inhibitory potential of oxadiazole derivatives

scientific article published on 07 March 2018

Synthesis, molecular docking study and thymidine phosphorylase inhibitory activity of 3-formylcoumarin derivatives

artículo científico publicado en 2018

Synthesis, molecular docking, acetylcholinesterase and butyrylcholinesterase inhibitory potential of thiazole analogs as new inhibitors for Alzheimer disease

artículo científico publicado en 2015

Synthesis, thymidine phosphorylase, angiogenic inhibition and molecular docking study of isoquinoline derivatives

artículo científico publicado en 2019

Synthesis, α-amylase inhibitory potential and molecular docking study of indole derivatives

artículo científico publicado en 2018

Synthesis, α-glucosidase inhibition and molecular docking study of coumarin based derivatives

artículo científico publicado en 2018

Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes mellitus.

artículo científico publicado en 2017

Synthesis, α-glucosidase inhibitory, cytotoxicity and docking studies of 2-aryl-7-methylbenzimidazoles

artículo científico publicado en 2016

Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs

artículo científico publicado en 2016

Synthesis,In vitroand Docking Studies of New Flavone Ethers asα-Glucosidase Inhibitors

artículo científico publicado en 2015

Synthesis: Small library of hybrid scaffolds of benzothiazole having hydrazone and evaluation of their β-glucuronidase activity

artículo científico publicado en 2018

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

artículo científico publicado en 2015

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

Triazinoindole analogs as potent inhibitors of α-glucosidase: synthesis, biological evaluation and molecular docking studies

artículo científico publicado en 2014

Lista de obras de Muhammad Taha

(E)-2,4-Dimethyl-N'-(2-methyl-benzyl-idene)benzohydrazide.

(E)-2-Meth-oxy-N'-(2,4,6-trihy-droxy-benzyl-idene)benzohydrazide.

(E)-3-Chloro-N'-(2-fluoro-benzyl-idene)thio-phene-2-carbohydrazide.

(E)-4-Meth-oxy-N'-(3,4,5-trihy-droxy-benzyl-idene)benzohydrazide methanol monosolvate.

(E)-4-Meth-oxy-N'-[(pyridin-4-yl)methyl-idene]benzohydrazide monohydrate

(E)-N'-(3,4-Dihy-droxy-benzyl-idene)-2,4-dimethyl-benzohydrazide monohydrate.

(E)-N'-(3,4-Dimeth-oxy-benzyl-idene)-4-meth-oxy-benzohydrazide.

(E)-N'-(4-Chloro-benzyl-idene)-2-meth-oxy-benzohydrazide.

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

2,5-Disubstituted thiadiazoles as potent β-glucuronidase inhibitors; Synthesis, in vitro and in silico studies

2-Aryl benzimidazoles: Synthesis, In vitro α-amylase inhibitory activity, and molecular docking study.

2-{[2-(2-Hy-droxy-5-meth-oxy-benzyl-idene)hydrazin-1-yl-idene]meth-yl}-4-meth-oxy-phenol.

3,4-Dimethoxybenzohydrazide derivatives as antiulcer: Molecular modeling and density functional studies.

3-[2-(Triphenyl-phosphanyl-idene)acet-yl]-2H-chromen-2-one.

5-Acetyl-6-methyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones: As potent urease inhibitors; synthesis, in vitro screening, and molecular modeling study

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

6-Nitrobenzimidazole derivatives: potential phosphodiesterase inhibitors: synthesis and structure-activity relationship

Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers

An expeditious synthetic approach towards the synthesis of Bis-Schiff bases (aldazines) using ultrasound.

Antibiofilm potential of synthetic 2-amino-5-chlorobenzophenone Schiff bases and its confirmation through fluorescence microscopy.

Antioxidant properties of phenolic Schiff bases: structure-activity relationship and mechanism of action.

Atenolol thiourea hybrid as potent urease inhibitors: Design, biology-oriented drug synthesis, inhibitory activity screening, and molecular docking studies

Benzimidazole derivatives as new α-glucosidase inhibitors and in silico studies.

Benzimidazole derivatives protect against cytokine-induced apoptosis in pancreatic β-Cells

Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies.

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.

Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies

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

Chalcones and bis-chalcones: As potential α-amylase inhibitors; synthesis, in vitro screening, and molecular modelling studies

Coumarin sulfonates: As potential leads for ROS inhibition

Crystal structure of (E)-N'-benzyl-idene-2-meth-oxy-benzohydrazide

Design, synthesis, in vitro evaluation, molecular docking and ADME properties studies of hybrid bis-coumarin with thiadiazole as a new inhibitor of Urease

Dihydropyrimidones: As novel class of β-glucuronidase inhibitors.

Evaluation of 2-indolcarbohydrazones as potent α-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions.

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

Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies

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

In silico binding analysis and SAR elucidations of newly designed benzopyrazine analogs as potent inhibitors of thymidine phosphorylase.

Indole bearing thiadiazole analogs: synthesis, β-glucuronidase inhibition and molecular docking study

Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies

Leishmanicidal potential of N-substituted morpholine derivatives: synthesis and structure-activity relationships

Methyl (E)-3,5-dimeth-oxy-2-{[2-(4-meth-oxy-benzo-yl)hydrazin-1-yl-idene]meth-yl}benzoate.

Molecular hybridization conceded exceptionally potent quinolinyl-oxadiazole hybrids through phenyl linked thiosemicarbazide antileishmanial scaffolds: In silico validation and SAR studies

N'-[(E)-2,3-Dihy-droxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

N'-[(E)-2-Hy-droxy-5-meth-oxy-benzyl-idene]-2-meth-oxy-benzohydrazide.

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

New triazinoindole bearing thiazole/oxazole analogues: Synthesis, α-amylase inhibitory potential and molecular docking study

Novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone: a new class of β-glucuronidase inhibitors and in silico studies.

Oxindole based oxadiazole hybrid analogs: Novel α-glucosidase inhibitors

Oxindole derivatives: synthesis and antiglycation activity

Phenoxyacetohydrazide Schiff bases: β-glucuronidase inhibitors

Rational design of bis-indolylmethane-oxadiazole hybrids as inhibitors of thymidine phosphorylase

Schiff bases of tryptamine as potent inhibitors of nucleoside triphosphate diphosphohydrolases (NTPDases): Structure-activity relationship

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

Synthesis and biological evaluation of indole derivatives as α-amylase inhibitor

Synthesis and biological evaluation of novel N-arylidenequinoline-3-carbohydrazides as potent β-glucuronidase inhibitors.

Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As β-glucuronidase inhibitors.

Synthesis and in vitro Leishmanicidal Activity of Disulfide Derivatives ⬇️

Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases

Synthesis and in vitro study of benzofuran hydrazone derivatives as novel alpha-amylase inhibitor

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 molecular docking study of piperazine derivatives as potent inhibitor of thymidine phosphorylase

Synthesis and molecular docking study of piperazine derivatives as potent urease inhibitors

Synthesis and molecular modelling studies of phenyl linked oxadiazole-phenylhydrazone hybrids as potent antileishmanial agents.

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

Synthesis and study of the α-amylase inhibitory potential of thiadiazole quinoline derivatives

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

Synthesis of 2,4,6-Trichlorophenyl Hydrazones and their Inhibitory Potential Against Glycation of Protein ⬇️

Synthesis of 2-acylated and sulfonated 4-hydroxycoumarins: In vitro urease inhibition and molecular docking studies

Synthesis of 2-methoxybenzoylhydrazone and evaluation of their antileishmanial activity

Synthesis of 3,4,5-trihydroxybenzohydrazone and evaluation of their urease inhibition potential

Synthesis of 4-methoxybenzoylhydrazones and evaluation of their antiglycation activity

Synthesis of 4-thiazolidinone analogs as potent in vitro anti-urease agents

Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies

Synthesis of Benzimidazole-Based Analogs as Anti Alzheimer's Disease Compounds and Their Molecular Docking Studies

Synthesis of Bis-indolylmethane sulfonohydrazides derivatives as potent α-Glucosidase inhibitors