about
Synthesis, biological evaluation, and molecular modeling of donepezil and N-[(5-(benzyloxy)-1-methyl-1H-indol-2-yl)methyl]-N-methylprop-2-yn-1-amine hybrids as new multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of AlzheimeReactivity versus steric effects in fluorinated ketones as esterase inhibitors: a quantum mechanical and molecular dynamics studyEnergetic contributions of residues to the formation of early amyloid-β oligomers.Molecular modelling of the differential interaction between several non-steroidal anti-inflammatory drugs and human prostaglandin endoperoxide H synthase-2 (h-PGHS-2).Structure-based QSAR study on differential inhibition of human prostaglandin endoperoxide H synthase-2 (COX-2) by nonsteroidal anti-inflammatory drugs.QSAR study of dual cyclooxygenase and 5-lipoxygenase inhibitors 2,6-di-tert-butylphenol derivatives.Evolution of a multicomponent system: computational and mechanistic studies on the chemo- and stereoselectivity of a divergent process.MMPBSA decomposition of the binding energy throughout a molecular dynamics simulation of amyloid-beta (Abeta(10-35)) aggregation.Determination of the encapsulation efficiency in liposomes obtained by the 'extruder method'Measurement of a glycoprotein with blood group A activity by light scatteringQSAR and conformational analysis of the antiinflammatory agent amfenac and analoguesThe structural and electronical factors that contribute affinity for the time-dependent inhibition of PGHS-1 by indomethacin, diclofenac and fenamatesSpectrophotometric determination of the stability of an ampicillin-dicloxacillin suspension
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Ramón Pouplana
@ast
Ramón Pouplana
@en
Ramón Pouplana
@es
Ramón Pouplana
@nl
type
label
Ramón Pouplana
@ast
Ramón Pouplana
@en
Ramón Pouplana
@es
Ramón Pouplana
@nl
prefLabel
Ramón Pouplana
@ast
Ramón Pouplana
@en
Ramón Pouplana
@es
Ramón Pouplana
@nl
P106
P31
P496
0000-0002-4770-5433