about
From Production of Peptides in Milligram Amounts for Research to Multi-Tons Quantities for Drugs of the FutureThiopeptide antibiotics: retrospective and recent advancesSynthesis and NMR structure of p41icf, a potent inhibitor of human cathepsin LA trifluorinated thiazoline scaffold leading to pro-apoptotic agents targeting prohibitinsNeurotoxicity of prion peptides mimicking the central domain of the cellular prion proteinAmide-to-ester substitution in coiled coils: the effect of removing hydrogen bonds on protein structure.Peptide dendrimers based on polyproline helices.Screening of N-alkyl-cyanoacetamido oximes as substitutes for N-hydroxysuccinimideStellatolides, a new cyclodepsipeptide family from the sponge Ecionemia acervus: isolation, solid-phase total synthesis, and full structural assignment of stellatolide A.Nsc and Fmoc Nalpha-amino protection for solid-phase peptide synthesis: a parallel study.Multicomponent reactions with dihydroazines: efficient synthesis of a diverse set of pyrido-fused tetrahydroquinolines.Tentoxin as a scaffold for drug discovery. Total solid-phase synthesis of tentoxin and a library of analogues.Morpholine-based immonium and halogenoamidinium salts as coupling reagents in Peptide synthesis1.Peptide and amide bond-containing dendrimers.Bicyclic homodetic peptide libraries: comparison of synthetic strategies for their solid-phase synthesis.Solid-phase synthesis and characterization of N-methyl-rich peptides.Synthesis and screening of a small library of proline-based biodendrimers for use as delivery agents.Evolutionary combinatorial chemistry, a novel tool for SAR studies on peptide transport across the blood-brain barrier. Part 2. Design, synthesis and evaluation of a first generation of peptides.Evaluation of solution and solid-phase approaches to the synthesis of libraries of alpha,alpha-disubstituted-alpha-acylaminoketones.ChemMatrix, a poly(ethylene glycol)-based support for the solid-phase synthesis of complex peptides.IB-01212, a new cytotoxic cyclodepsipeptide isolated from the marine fungus Clonostachys sp. ESNA-A009.Total solid-phase synthesis of the azathiocoraline class of symmetric bicyclic peptides.New efficient substrates for semicarbazide-sensitive amine oxidase/VAP-1 enzyme: analysis by SARs and computational docking.Smallest peptoids with antiproliferative activity on human neoplastic cells.Novel ergopeptides as dual ligands for adenosine and dopamine receptors.Identification of protein-binding peptides by direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry analysis of peptide beads selected from the screening of one bead-one peptide combinatorial libraries.Solid-phase combinatorial synthesis of a lysyl-tRNA synthetase (LysRS) inhibitory library.Design and synthesis of FAJANU: a de novo C(2) symmetric cyclopeptide family.Phakellistatins: An Underwater Unsolved Puzzle.Synthesis and antitumor activity of mechercharmycin A analogues.Screening of one-bead-one-peptide combinatorial library using red fluorescent dyes. Presence of positive and false positive beads.COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents.Adenosine A2A receptor-antagonist/dopamine D2 receptor-agonist bivalent ligands as pharmacological tools to detect A2A-D2 receptor heteromers.COMU: a third generation of uronium-type coupling reagents.Microwave assisted SPPS of amylin and its toxicity of the pure product to RIN-5F cells.Sample preparation for sequencing hits from one-bead-one-peptide combinatorial libraries by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.Tetrahydropyranyl: A Non-aromatic, Mild-Acid-Labile Group for Hydroxyl Protection in Solid-Phase Peptide Synthesis.Understanding Tetrahydropyranyl as a Protecting Group in Peptide Chemistry.Affinity chromatography based on a combinatorial strategy for rerythropoietin purification.TRPV1 modulators: structure-activity relationships using a rational combinatorial approach.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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ricercatore
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հետազոտող
@hy
name
Fernando Albericio
@ast
Fernando Albericio
@en
Fernando Albericio
@es
Fernando Albericio
@nl
Fernando Albericio
@sl
type
label
Fernando Albericio
@ast
Fernando Albericio
@en
Fernando Albericio
@es
Fernando Albericio
@nl
Fernando Albericio
@sl
prefLabel
Fernando Albericio
@ast
Fernando Albericio
@en
Fernando Albericio
@es
Fernando Albericio
@nl
Fernando Albericio
@sl
P1006
P214
P244
P1006
P1053
B-4383-2013
P106
P1153
7005138070
P1580
P21
P213
0000 0001 1652 0850
P214
P244
P31
P3829
P496
0000-0002-8946-0462
P735
P7859
lccn-n97013881