Lista de obras - Fazeer Sheik Rahim - Dominio Público Uruguay

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

artículo científico publicado en 2017

Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers

artículo científico publicado en 2012

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

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

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

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

artículo científico publicado en 2016

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

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

artículo científico publicado en 2016

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

scientific article published on 04 May 2014

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 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 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 indole analogs as potent β-glucuronidase inhibitors.

artículo científico publicado en 2017

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

scientific article published on 26 October 2015

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

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 α-glucosidase inhibitory potential and molecular docking study of thiadiazole analogs

artículo científico publicado en 2018

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, 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

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

Lista de obras de Fazeer Sheik Rahim

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

Acylhydrazide Schiff bases: DPPH radical and superoxide anion scavengers

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

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.

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

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

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

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

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

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 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

Synthesis of alpha amylase inhibitors based on privileged indole scaffold

Synthesis of benzimidazole derivatives as potent β-glucuronidase inhibitors

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

Synthesis of indole analogs as potent β-glucuronidase inhibitors.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

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