Lista de obras - Sandeep Sundriyal - Dominio Público Uruguay

'Sum of activities' as dependent parameter: a new CoMFA-based approach for the design of pan PPAR agonists

artículo científico publicado en 2008

2-Substituted 4,5-dihydrothiazole-4-carboxylic acids are novel inhibitors of metallo-β-lactamases

artículo científico publicado en 2012

Apicoplast isoprenoid precursor synthesis and the molecular basis of fosmidomycin resistance in Toxoplasma gondii.

artículo científico publicado en 2011

Apicoplast isoprenoid precursor synthesis and the molecular basis of fosmidomycin resistance inToxoplasma gondii

scholarly article by Sethu C. Nair et al published 30 April 2012 in Journal of Experimental Medicine

Conformational polymorphism in sulfonylurea drugs: electronic structure analysis.

artículo científico publicado en 2010

Coordination chemistry based approach to lipophilic inhibitors of 1-deoxy-D-xylulose-5-phosphate reductoisomerase.

artículo científico publicado en 2009

Current advances in antifungal targets and drug development

artículo científico publicado en 2006

Development of diaminoquinazoline histone lysine methyltransferase inhibitors as potent blood-stage antimalarial compounds

artículo científico publicado en 2014

Histone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-Plasmodium activity

artículo científico publicado en 2017

Histone methyltransferase inhibitors are orally bioavailable, fast-acting molecules with activity against different species causing malaria in humans

artículo científico publicado en 2014

Identification of 2,4-diamino-6,7-dimethoxyquinoline derivatives as G9a inhibitors†Electronic supplementary information (ESI) available. See DOI: 10.1039/c4md00274a.

artículo científico publicado en 2014

Identification of antimalarial leads with dual falcipain-2 and falcipain-3 inhibitory activity

scientific article published on 09 November 2019

Important pharmacophoric features of pan PPAR agonists: common chemical feature analysis and virtual screening

artículo científico publicado en 2009

Minimum requirements of hydrophobic and hydrophilic features in cationic peptide antibiotics (CPAs): pharmacophore generation and validation with cationic steroid antibiotics (CSAs).

artículo científico publicado en 2008

Modeling and informatics in designing anti-diabetic agents

artículo científico publicado en 2007

Molecular electrostatic potentials in the design of dendrimers for the delivery of glitazones

scientific article published on 01 September 2006

New PPARgamma ligands based on 2-hydroxy-1,4-naphthoquinone: computer-aided design, synthesis, and receptor-binding studies

artículo científico publicado en 2008

New PPARgamma ligands based on barbituric acid: virtual screening, synthesis and receptor binding studies

artículo científico publicado en 2008

New antimicrobial hexapeptides: synthesis, antimicrobial activities, cytotoxicity, and mechanistic studies

artículo científico publicado en 2010

On the histone lysine methyltransferase activity of fungal metabolite chaetocin.

artículo científico publicado en 2013

Thienopyrimidinone Based Sirtuin-2 (SIRT2)-Selective Inhibitors Bind in the Ligand Induced Selectivity Pocket.

artículo científico publicado en 2017

Lista de obras de Sandeep Sundriyal

'Sum of activities' as dependent parameter: a new CoMFA-based approach for the design of pan PPAR agonists

2-Substituted 4,5-dihydrothiazole-4-carboxylic acids are novel inhibitors of metallo-β-lactamases

Apicoplast isoprenoid precursor synthesis and the molecular basis of fosmidomycin resistance in Toxoplasma gondii.

Apicoplast isoprenoid precursor synthesis and the molecular basis of fosmidomycin resistance inToxoplasma gondii

Conformational polymorphism in sulfonylurea drugs: electronic structure analysis.

Coordination chemistry based approach to lipophilic inhibitors of 1-deoxy-D-xylulose-5-phosphate reductoisomerase.

Current advances in antifungal targets and drug development

Development of diaminoquinazoline histone lysine methyltransferase inhibitors as potent blood-stage antimalarial compounds

Histone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-Plasmodium activity

Histone methyltransferase inhibitors are orally bioavailable, fast-acting molecules with activity against different species causing malaria in humans

Identification of 2,4-diamino-6,7-dimethoxyquinoline derivatives as G9a inhibitors†Electronic supplementary information (ESI) available. See DOI: 10.1039/c4md00274a.

Identification of antimalarial leads with dual falcipain-2 and falcipain-3 inhibitory activity

Important pharmacophoric features of pan PPAR agonists: common chemical feature analysis and virtual screening

Minimum requirements of hydrophobic and hydrophilic features in cationic peptide antibiotics (CPAs): pharmacophore generation and validation with cationic steroid antibiotics (CSAs).

Modeling and informatics in designing anti-diabetic agents

Molecular electrostatic potentials in the design of dendrimers for the delivery of glitazones

New PPARgamma ligands based on 2-hydroxy-1,4-naphthoquinone: computer-aided design, synthesis, and receptor-binding studies

New PPARgamma ligands based on barbituric acid: virtual screening, synthesis and receptor binding studies

New antimicrobial hexapeptides: synthesis, antimicrobial activities, cytotoxicity, and mechanistic studies

On the histone lysine methyltransferase activity of fungal metabolite chaetocin.

Thienopyrimidinone Based Sirtuin-2 (SIRT2)-Selective Inhibitors Bind in the Ligand Induced Selectivity Pocket.