Lista de obras - Julie Charton - Dominio Público Uruguay

A library of novel hydroxamic acids targeting the metallo-protease family: design, parallel synthesis and screening

artículo científico publicado en 2006

A versatile solid-phase synthesis of 3-aryl-1,2,4-oxadiazolones and analogues

Access to newly functionalized imidazole derivatives: efficient synthesis of novel 5-amino-2-thioimidazoles using propylphosphonic anhydride (®T3P)

Alkylsquarates as key intermediates for the rapid preparation of original drug-inspired compounds

artículo científico publicado en 2008

Catalytic site inhibition of insulin-degrading enzyme by a small molecule induces glucose intolerance in mice

artículo científico publicado en 2015

Characterization of monoclonal antibodies by a fast and easy liquid chromatography-mass spectrometry time-of-flight analysis on culture supernatant

artículo científico publicado en 2015

Convenient synthesis of 4H-1,2,4-triazole-3-thiols using di-2-pyridylthionocarbonate

Convenient synthesis of tetrahydroisoquinoline-hydantoins

article published in 2001

Conversion of sterically hindered diacylated 1,2-phenylenediamines into 2-substituted benzimidazoles

artículo científico publicado en 2005

Determination of pKa values of benzimidazole derivatives from mobility obtained by capillary electrophoresis

artículo científico publicado en 2010

Development of HPLC/fluorescence detection method for chiral resolution of dansylated benzimidazoles derivatives

artículo científico publicado en 2013

Drug to Genome to Drug: Discovery of New Antiplasmodial Compounds

artículo científico publicado en 2011

Drug-to-genome-to-drug, step 2: reversing selectivity in a series of antiplasmodial compounds

artículo científico publicado en 2012

Enantioseparation of chiral benzimidazole derivatives by electrokinetic chromatography using sulfated cyclodextrins.

artículo científico publicado en 2009

Hydroxamates: relationships between structure and plasma stability

artículo científico publicado en 2009

Imidazole-derived 2-[N-carbamoylmethyl-alkylamino]acetic acids, substrate-dependent modulators of insulin-degrading enzyme in amyloid-β hydrolysis

artículo científico publicado en 2014

Novel non-carboxylic acid retinoids: 1,2,4-oxadiazol-5-one derivatives

artículo científico publicado en 2008

Optimized synthesis of tetrahydroisoquinoline-hydantoins

Preparative enantiomeric separation of potent AMP-activated protein kinase activator by HPLC on amylose-based chiral stationary phase. Determination of enantiomeric purity and assignment of absolute configuration

artículo científico publicado en 2008

Single and dual cyclodextrins systems for the enantiomeric and diastereoisomeric separations of structurally related dihydropyridone analogues

artículo científico publicado en 2017

Squaric acid is a suitable building-block in 4C-Ugi reaction: access to original bivalent compounds

Structure-activity relationships of imidazole-derived 2-[N-carbamoylmethyl-alkylamino]acetic acids, dual binders of human insulin-degrading enzyme.

artículo científico publicado en 2014

Supercritical fluid chromatography versus high performance liquid chromatography for enantiomeric and diastereoisomeric separations on coated polysaccharides-based stationary phases: Application to dihydropyridone derivatives

artículo científico publicado en 2018

Synthesis and biological evaluation of benzimidazole derivatives as potent AMP-activated protein kinase activators

artículo científico publicado en 2006

Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective sigma1 ligands. Part 2.

artículo científico publicado en 2005

Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective σ1 ligands. Part 1

artículo científico publicado en 2005

Synthesis of a 200-member library of squaric acid N-hydroxylamide amides

artículo científico publicado en 2008

The Bile Acid Chenodeoxycholic Acid Increases Human Brown Adipose Tissue Activity

artículo científico publicado en 2015

Topical Intestinal Aminoimidazole Agonists of G-Protein-Coupled Bile Acid Receptor 1 Promote Glucagon Like Peptide-1 Secretion and Improve Glucose Tolerance

artículo científico publicado en 2017

Lista de obras de Julie Charton

A library of novel hydroxamic acids targeting the metallo-protease family: design, parallel synthesis and screening

A versatile solid-phase synthesis of 3-aryl-1,2,4-oxadiazolones and analogues

Access to newly functionalized imidazole derivatives: efficient synthesis of novel 5-amino-2-thioimidazoles using propylphosphonic anhydride (®T3P)

Alkylsquarates as key intermediates for the rapid preparation of original drug-inspired compounds

Catalytic site inhibition of insulin-degrading enzyme by a small molecule induces glucose intolerance in mice

Characterization of monoclonal antibodies by a fast and easy liquid chromatography-mass spectrometry time-of-flight analysis on culture supernatant

Convenient synthesis of 4H-1,2,4-triazole-3-thiols using di-2-pyridylthionocarbonate

Convenient synthesis of tetrahydroisoquinoline-hydantoins

Conversion of sterically hindered diacylated 1,2-phenylenediamines into 2-substituted benzimidazoles

Determination of pKa values of benzimidazole derivatives from mobility obtained by capillary electrophoresis

Development of HPLC/fluorescence detection method for chiral resolution of dansylated benzimidazoles derivatives

Drug to Genome to Drug: Discovery of New Antiplasmodial Compounds

Drug-to-genome-to-drug, step 2: reversing selectivity in a series of antiplasmodial compounds

Enantioseparation of chiral benzimidazole derivatives by electrokinetic chromatography using sulfated cyclodextrins.

Hydroxamates: relationships between structure and plasma stability

Imidazole-derived 2-[N-carbamoylmethyl-alkylamino]acetic acids, substrate-dependent modulators of insulin-degrading enzyme in amyloid-β hydrolysis

Novel non-carboxylic acid retinoids: 1,2,4-oxadiazol-5-one derivatives

Optimized synthesis of tetrahydroisoquinoline-hydantoins

Preparative enantiomeric separation of potent AMP-activated protein kinase activator by HPLC on amylose-based chiral stationary phase. Determination of enantiomeric purity and assignment of absolute configuration

Single and dual cyclodextrins systems for the enantiomeric and diastereoisomeric separations of structurally related dihydropyridone analogues

Squaric acid is a suitable building-block in 4C-Ugi reaction: access to original bivalent compounds

Structure-activity relationships of imidazole-derived 2-[N-carbamoylmethyl-alkylamino]acetic acids, dual binders of human insulin-degrading enzyme.

Supercritical fluid chromatography versus high performance liquid chromatography for enantiomeric and diastereoisomeric separations on coated polysaccharides-based stationary phases: Application to dihydropyridone derivatives

Synthesis and biological evaluation of benzimidazole derivatives as potent AMP-activated protein kinase activators

Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective sigma1 ligands. Part 2.

Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective σ1 ligands. Part 1

Synthesis of a 200-member library of squaric acid N-hydroxylamide amides

The Bile Acid Chenodeoxycholic Acid Increases Human Brown Adipose Tissue Activity

Topical Intestinal Aminoimidazole Agonists of G-Protein-Coupled Bile Acid Receptor 1 Promote Glucagon Like Peptide-1 Secretion and Improve Glucose Tolerance