about
Spiroimidazolidinone library derivatives on SynPhase lanterns.Improvement of cyclic decapeptides against plant pathogenic bacteria using a combinatorial chemistry approach.On-line synthesis of pseudopeptide library incorporating a benzodiazepinone turn mimic: biological evaluation on MC1 receptors.A library of linear undecapeptides with bactericidal activity against phytopathogenic bacteria.Sporicidal activity of synthetic antifungal undecapeptides and control of Penicillium rot of applesPrediction of antibacterial activity from physicochemical properties of antimicrobial peptides.Inhibition of plant-pathogenic bacteria by short synthetic cecropin A-melittin hybrid peptidesDerivatives of the antimicrobial peptide BP100 for expression in plant systems.Synthetic Cyclolipopeptides Selective against Microbial, Plant and Animal Cell Targets by Incorporation of D-Amino Acids or HistidineAdvances in solid-phase cycloadditions for heterocyclic synthesis.Antimicrobial peptides incorporating non-natural amino acids as agents for plant protection.Enzyme-triggered delivery of chlorambucil from conjugates based on the cell-penetrating peptide BP16.Identification of BP16 as a non-toxic cell-penetrating peptide with highly efficient drug delivery properties.Synergistic effects of the membrane actions of cecropin-melittin antimicrobial hybrid peptide BP100Escherichia coli cell surface perturbation and disruption induced by antimicrobial peptides BP100 and pepRImprovement of the efficacy of linear undecapeptides against plant-pathogenic bacteria by incorporation of D-amino acids.A convenient solid-phase strategy for the synthesis of antimicrobial cyclic lipopeptides.Synthesis and Biological Evaluation of Ru(II) and Pt(II) Complexes Bearing Carboxyl Groups as Potential Anticancer Targeted Drugs.Tryptophan-Containing Cyclic Decapeptides with Activity against Plant Pathogenic Bacteria.Rational Design of Cyclic Antimicrobial Peptides Based on BPC194 and BPC198.Solid-Phase Synthesis of Cyclic Depsipeptides Containing a Tyrosine Phenyl Ester Bond.Delivering aminopyridine ligands into cancer cells through conjugation to the cell-penetrating peptide BP16.Peptide-mediated vectorization of metal complexes: conjugation strategies and biomedical applications.Design, Preparation, and Characterization of Zn and Cu Metallopeptides Based On Tetradentate Aminopyridine Ligands Showing Enhanced DNA Cleavage Activity.Solid-phase synthesis of 5-arylhistidines via a microwave-assisted Suzuki–Miyaura cross-couplingSynthesis of an 8-Benzyl-4-(p-substituted-benzyl)-1,4,8-triazaspiro[4.5]decan-2-one Library on SynPhase TMLanternsOptimization of spiroimidazolidinone derivatives synthesis on solid phase using SynPhase™ LanternsComparison of migration disturbance potency of epigallocatechin gallate (EGCG) synthetic analogs and EGCG PEGylated PLGA nanoparticles in rat neurospheresPeptidotriazoles with antimicrobial activity against bacterial and fungal plant pathogensSolid-Phase Synthesis of Biaryl Cyclic Peptides Containing a 3-AryltyrosineSolid-phase synthesis of biaryl bicyclic peptides containing a 3-aryltyrosine or a 4-arylphenylalanine moietyEGCG-Derivative G28 Shows High Efficacy Inhibiting the Mammosphere-Forming Capacity of Sensitive and Resistant TNBC ModelsStructural basis for the enhanced activity of cyclic antimicrobial peptides: the case of BPC194(-)-Epigallocatechin 3-Gallate Synthetic Analogues Inhibit Fatty Acid Synthase and Show Anticancer Activity in Triple Negative Breast CancerDesign, synthesis, and biological evaluation of cyclic peptidotriazoles derived from BPC194 as novel agents for plant protectionAntimicrobial peptide KSL-W and analogues: Promising agents to control plant diseasesTotal Solid-Phase Synthesis of Dehydroxy Fengycin DerivativesAntimicrobial activity of linear lipopeptides derived from BP100 towards plant pathogens
P50
Q31149359-BCA9C443-E2A9-4A34-AA2E-E81D075AD906Q33246209-F345DCF0-4F2F-4BC5-B751-0F4EC4165E37Q33277629-4DBC7CD1-E703-4B5D-8CE4-E5A2C397C8D1Q33304920-36C400C1-D3CA-4892-A362-E15449F40CEAQ33484091-2F79B816-7749-4EC0-86EC-3CDBD37F228AQ34110097-14BB6261-1E1D-44FC-9EE5-65089E0CC5CCQ34649469-E80E54AA-B786-4E51-889B-2927ABDEFB15Q35078607-CC6D46F8-4301-4E98-A10B-BB9F4C8593D8Q35967862-659E7389-CAA9-41DC-9A81-4AC3F5DC617FQ36819762-36DF6508-587B-41C0-B6C5-1ACB529FF17EQ38155900-8EA38B28-FCA8-47A9-AA82-05D48D6E0853Q38932275-32FECD45-2B5B-4AF6-BD33-FE21807B5A3CQ39028900-5956768E-E136-427F-82E9-50729F984936Q39878043-A8ABB961-1D10-4795-985F-FC4B55EEC79BQ40355921-F816601D-428C-4C0E-90B1-58CD1E56C0B2Q42246168-17D35190-148D-4FC4-8983-A52156C1AAF0Q46920049-BCA4D180-DAAD-4D78-8A9F-5FF3E9DEDA17Q47664079-909B0D96-9B13-4DA2-9180-28BFBDABDC08Q47714243-750B3870-05A7-48B7-9E11-38A5BA0DD7BAQ48734845-FD31E0FA-6755-4023-ABB2-98126B44BB66Q50776480-719C981C-4D33-4306-81F5-5A7617D3E873Q50857768-E982E37D-4531-4C77-B207-0A2D70FE0EC9Q50860069-A3783681-553C-4A5D-B6E7-418F6B84E81EQ52906863-807F2578-D72A-4A8E-BC98-EAB44BB7785CQ58102196-40835D8B-1A49-4AE6-9AF3-5C730D8C31D3Q58103154-4D12CBBD-8D83-4242-B83B-2DCF8FCD3E4AQ58103252-0D9D5411-E41D-4495-958F-2D770E56A267Q58118297-27E65653-9669-4724-A663-538D67CDA794Q63315464-41741DC0-05C3-4054-AC6B-0FD7F8D8BD36Q63982460-6A0B6E73-B02F-452E-B64C-15A29A835A74Q64059481-A45E962D-2CBE-4A1F-BB14-F3368DADF2DCQ64089216-43A207BC-B9AD-4D64-8ABB-0F454741A2EBQ84131050-B48BA3A5-71E2-4088-ADD8-A31EECF2B2D2Q88643680-E65CF5BC-C1B0-4FD2-B3E7-A934676A4D5CQ89347856-54985ADF-6572-4D05-A483-86D4979EF22EQ90217947-58978339-2E34-4BEB-8FF4-499223DCB1D4Q90331505-4AAFDD95-DDF5-4B0B-A371-730D1182A018Q90568731-D8D92CEA-35EC-4CE1-9083-EAE857ECD927
P50
description
hulumtuese
@sq
researcher
@en
ricercatrice
@it
wetenschapper
@nl
հետազոտող
@hy
name
Lidia Feliu
@ast
Lidia Feliu
@en
Lidia Feliu
@es
Lidia Feliu
@nl
Lidia Feliu
@sl
type
label
Lidia Feliu
@ast
Lidia Feliu
@en
Lidia Feliu
@es
Lidia Feliu
@nl
Lidia Feliu
@sl
prefLabel
Lidia Feliu
@ast
Lidia Feliu
@en
Lidia Feliu
@es
Lidia Feliu
@nl
Lidia Feliu
@sl
P214
P106
P1153
9042517300
P1580
P21
P214
P31
P496
0000-0001-9792-6106
P735
P7859
viaf-305868450