Lista de obras -

11-Keto-β-Boswellic Acids Prevent Development of Autoimmune Reactions, Insulitis and Reduce Hyperglycemia During Induction of Multiple Low-Dose Streptozotocin (MLD-STZ) Diabetes in Mice

artículo científico publicado en 2015

A residue W756 in the P-loop segment of the sodium channel is critical for primaquine binding.

artículo científico publicado en 2011

Antiprotozoal Nitazoxanide Derivatives: Synthesis, Bioassays and QSAR Study Combined with Docking for Mechanistic Insight.

artículo científico publicado en 2015

Application of drug repositioning strategy to TOFISOPAM.

artículo científico publicado en 2008

Are vanadium compounds drugable? Structures and effects of antidiabetic vanadium compounds: a critical review.

artículo científico publicado en 2005

Characterization of specific allosteric effects of the Na+ channel β1 subunit on the Nav1.4 isoform

artículo científico publicado en 2016

Chemometric Models of Differential Amino Acids at the Navα and Navβ Interface of Mammalian Sodium Channel Isoforms

artículo científico publicado en 2020

Chimeric design, synthesis, and biological assays of a new nonpeptide insulin-mimetic vanadium compound to inhibit protein tyrosine phosphatase 1B ⬇️

artículo científico publicado el 24 de septiembre de 2010

Computational Binding Study Hints at Ecdysone 20-Mono-Oxygenase as the Hitherto Unknown Target for Ring C-Seco Limonoid-Type Insecticides

artículo científico publicado en 2024

Elucidation of the fragmentation pathways of different phosphatidylinositol phosphate species (PIPx) using IRMPD implemented on a FT-ICR MS.

artículo científico publicado en 2010

Ethnopharmacology and bioinformatic combination for leads discovery: application to phospholipase A2 inhibitors ⬇️

artículo científico publicado el 1 de noviembre de 2001

Exploring electrostatic patterns of human, murine, equine and canine TLR4/MD-2 receptors

artículo científico publicado en 2019

Five Novel Non-Sialic Acid-Like Scaffolds Inhibit In Vitro H1N1 and H5N2 Neuraminidase Activity of Influenza a Virus

scientific article published on 16 September 2020

How to Valorize Biodiversity? Let's Go Hashing, Extracting, Filtering, Mining, Fishing.

artículo científico publicado en 2015

How to recognize and workaround pitfalls in QSAR studies: a critical review

scientific article published on January 2009

Identification of Navβ1 residues involved in the modulation of the sodium channel Nav1.4.

artículo científico publicado en 2013

Integrating computational and mixture-based screening of combinatorial libraries.

artículo científico publicado en 2010

Interference of boswellic acids with the ligand binding domain of the glucocorticoid receptor

artículo científico publicado en 2014

Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: a critical review.

artículo científico publicado en 2006

Large compound databases for structure-activity relationships studies in drug discovery.

artículo científico publicado en 2007

Mefloquine inhibits voltage dependent Nav1.4 channel by overlapping the local anaesthetic binding site.

artículo científico publicado en 2017

Modulating testosterone pathway: a new strategy to tackle male skin aging?

artículo científico publicado en 2012

Pharmacophore design of p38α MAP kinase inhibitors with either 2,4,5-trisubstituted or 1,2,4,5-tetrasubstituted imidazole scaffold.

artículo científico publicado en 2011

Predicting a double mutant in the twilight zone of low homology modeling for the skeletal muscle voltage-gated sodium channel subunit beta-1 (Nav1.4 β1).

artículo científico publicado en 2015

Prolyl isomerases in a minimal cell. Catalysis of protein folding by trigger factor from Mycoplasma genitalium.

artículo científico publicado en 2000

Reverse pharmacognosy: another way to harness the generosity of nature

artículo científico publicado en 2010

Reviewing and identifying amino acids of human, murine, canine and equine TLR4 / MD-2 receptor complexes conferring endotoxic innate immunity activation by LPS/lipid A, or antagonistic effects by Eritoran, in contrast to species-dependent modulation

artículo científico

Synthesis and biological testing of purine derivatives as potential ATP-competitive kinase inhibitors.

artículo científico publicado en 2005

Synthesis, biological testing, and binding mode prediction of 6,9-diarylpurin-8-ones as p38 MAP kinase inhibitors

scientific article published on 06 April 2007

Three-dimensional mapping of differential amino acids of human, murine, canine and equine TLR4/MD-2 receptor complexes conferring endotoxic activation by lipid A, antagonism by Eritoran and species-dependent activities of Lipid IVA in the mammalian L

artículo científico publicado en 2013

Why Antidiabetic Vanadium Complexes are Not in the Pipeline of "Big Pharma" Drug Research? A Critical Review

artículo científico publicado en 2016

Lista de obras de

11-Keto-β-Boswellic Acids Prevent Development of Autoimmune Reactions, Insulitis and Reduce Hyperglycemia During Induction of Multiple Low-Dose Streptozotocin (MLD-STZ) Diabetes in Mice

A residue W756 in the P-loop segment of the sodium channel is critical for primaquine binding.

Antiprotozoal Nitazoxanide Derivatives: Synthesis, Bioassays and QSAR Study Combined with Docking for Mechanistic Insight.

Application of drug repositioning strategy to TOFISOPAM.

Are vanadium compounds drugable? Structures and effects of antidiabetic vanadium compounds: a critical review.

Characterization of specific allosteric effects of the Na+ channel β1 subunit on the Nav1.4 isoform

Chemometric Models of Differential Amino Acids at the Navα and Navβ Interface of Mammalian Sodium Channel Isoforms

Chimeric design, synthesis, and biological assays of a new nonpeptide insulin-mimetic vanadium compound to inhibit protein tyrosine phosphatase 1B ⬇️

Computational Binding Study Hints at Ecdysone 20-Mono-Oxygenase as the Hitherto Unknown Target for Ring C-Seco Limonoid-Type Insecticides

Elucidation of the fragmentation pathways of different phosphatidylinositol phosphate species (PIPx) using IRMPD implemented on a FT-ICR MS.

Ethnopharmacology and bioinformatic combination for leads discovery: application to phospholipase A2 inhibitors ⬇️

Exploring electrostatic patterns of human, murine, equine and canine TLR4/MD-2 receptors

Five Novel Non-Sialic Acid-Like Scaffolds Inhibit In Vitro H1N1 and H5N2 Neuraminidase Activity of Influenza a Virus

How to Valorize Biodiversity? Let's Go Hashing, Extracting, Filtering, Mining, Fishing.

How to recognize and workaround pitfalls in QSAR studies: a critical review

Identification of Navβ1 residues involved in the modulation of the sodium channel Nav1.4.

Integrating computational and mixture-based screening of combinatorial libraries.

Interference of boswellic acids with the ligand binding domain of the glucocorticoid receptor

Isoniazid is not a lead compound for its pyridyl ring derivatives, isonicotinoyl amides, hydrazides, and hydrazones: a critical review.

Large compound databases for structure-activity relationships studies in drug discovery.

Mefloquine inhibits voltage dependent Nav1.4 channel by overlapping the local anaesthetic binding site.

Modulating testosterone pathway: a new strategy to tackle male skin aging?

Pharmacophore design of p38α MAP kinase inhibitors with either 2,4,5-trisubstituted or 1,2,4,5-tetrasubstituted imidazole scaffold.

Predicting a double mutant in the twilight zone of low homology modeling for the skeletal muscle voltage-gated sodium channel subunit beta-1 (Nav1.4 β1).

Prolyl isomerases in a minimal cell. Catalysis of protein folding by trigger factor from Mycoplasma genitalium.

Reverse pharmacognosy: another way to harness the generosity of nature

Reviewing and identifying amino acids of human, murine, canine and equine TLR4 / MD-2 receptor complexes conferring endotoxic innate immunity activation by LPS/lipid A, or antagonistic effects by Eritoran, in contrast to species-dependent modulation

Synthesis and biological testing of purine derivatives as potential ATP-competitive kinase inhibitors.

Synthesis, biological testing, and binding mode prediction of 6,9-diarylpurin-8-ones as p38 MAP kinase inhibitors

Three-dimensional mapping of differential amino acids of human, murine, canine and equine TLR4/MD-2 receptor complexes conferring endotoxic activation by lipid A, antagonism by Eritoran and species-dependent activities of Lipid IVA in the mammalian L

Why Antidiabetic Vanadium Complexes are Not in the Pipeline of "Big Pharma" Drug Research? A Critical Review