Now showing items 21-30 of 116
Identification Of A New Hormone-binding Site On The Surface Of Thyroid Hormone Receptor
(Endocrine Society, 2014)
NNAlign-MA; MHC peptidome deconvolution for accurate MHC binding motif characterization and improved t-cell epitope predictions
(American Society for Biochemistry and Molecular Biology, 2019-10)
The set of peptides presented on a cell´s surface by MHC molecules is known as the immunopeptidome. Current mass spectrometry technologies allow for identification of large peptidomes, and studies have proven these data ...
Novel green and more efficient reaction for the synthesis of aromatic hydrazides
(Sociedade Brasileira de Química, 2022)
Development of new lanthanide-based sensors depends on the rational design of ligands containing multiple coordination sites and planar π-delocalized systems for light reception. In this work we present a novel, one-step ...
Dynamic active site modeling for efficient drug design of human acetylcholinesterase inhibitors: an approach based on pharmacophore modeling and experimental data
(Universidad de los AndesMaestría en Ingeniería QuímicaFacultad de Ingeniería, 2023-05-30)
El aumento en la esperanza de vida de la población mundial ha impulsado el descubrimiento de nuevas enfermedades relacionadas con el envejecimiento, como la enfermedad de Alzheimer (EA). Esto ha llevado a la comunidad ...
Lumican Peptides: Rational Design Targeting ALK5/TGFBRI
(Nature Publishing Group, 2017)
Lumican, a small leucine rich proteoglycan (SLRP), is a component of extracellular matrix which also functions as a matrikine regulating multiple cell activities. In the cornea, lumican maintains corneal transparency by ...
Computer-aided drug design against spike glycoprotein of SARS-CoV-2 to aid COVID-19 treatment
Background: SARS-CoV-2 has the Spike glycoprotein (S) which is crucial in attachment with host receptor and cell entry leading to COVID-19 infection. The current study was conducted to explore drugs against Receptor ...
Three-dimensional QSAR analysis and design of new 1,2,4-oxadiazole antibacterials
(Pergamon-Elsevier Science Ltd, 2016-01)
The oxadiazole antibacterials, a class of newly discovered compounds that are active against Gram-positive bacteria, target bacterial cell-wall biosynthesis by inhibition of a family of essential enzymes, the penicillin-binding ...
Design, synthesis and evaluation of cholinesterase hybrid inhibitors using a natural steroidal alkaloid as precursor
(Academic Press Inc Elsevier Science, 2021-06-11)
To date, Alzheimers disease is the most alarming neurodegenerative disorder worldwide. This illness is multifactorialin nature and cholinesterase inhibitors have been the ones used in clinical treatments. In this context,many ...