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A complete set of NMR chemical shifts and spin-spin coupling constants for L-Alanyl-L-alanine zwitterion and analysis of its conformational behavior.Rational design and synthesis of a double-stranded DNA-binder library.Glycopeptide dendrimers. Part II.Conformational properties of the Pro-Gly motif in the D-Ala-l-Pro-Gly-D-Ala model peptide explored by a statistical analysis of the NMR, Raman, and Raman optical activity spectra.Peptide and glycopeptide dendrimers and analogous dendrimeric structures and their biomedical applications.Resolution of organic polymorphic crystals by Raman spectroscopy.Intense chirality induction in nitrile solvents by a helquat dye monitored by near resonance Raman scattering.Molecular recognition of cyclic-nucleotides and current sensors for their detection.Peptide dendrimers.New peptide conjugates with 9-aminoacridine: synthesis and binding to DNA.Ramachandran Plot for Alanine Dipeptide as Determined from Raman Optical Activity.Ferric complexes of 3-hydroxy-4-pyridinones characterized by density functional theory and Raman and UV-vis spectroscopies.Interpretation of synchrotron radiation circular dichroism spectra of anionic, cationic, and zwitterionic dialanine forms.Comparative syntheses of peptides and peptide thioesters derived from mouse and human prion proteins.L-alanyl-L-alanine conformational changes induced by pH as monitored by the Raman optical activity spectra.New tripodal hydroxypyridinone based chelating agents for Fe(III), Al(III) and Ga(III): Synthesis, physico-chemical properties and bioevaluation.Dependence of the L-alanyl-L-alanine conformation on molecular charge determined from ab initio computations and NMR spectra.Diamagnetic Raman Optical Activity of Chlorine, Bromine, and Iodine Gases.Resolving Electronic Transitions in Synthetic Fluorescent Protein Chromophores by Magnetic Circular Dichroism.Rapid acidolysis of benzyl group as a suitable approach for syntheses of peptides naturally produced by oxidative stress and containing 3-nitrotyrosine.Reactivity of 9-aminoacridine drug quinacrine with glutathione limits its antiprion activity.Binding of Lanthanide Complexes to Histidine-Containing Peptides Inspected by Raman Optical Activity Spectroscopy.Glutamate carboxypeptidase II does not process amyloid-β peptide.Bifunctional phenolic-choline conjugates as anti-oxidants and acetylcholinesterase inhibitorsObservation of paramagnetic Raman optical activity of nitrogen dioxideDetermining the Absolute Configuration of Two Marine Compounds Using Vibrational Chiroptical SpectroscopyVibrational Optical Activity of Intermolecular, Overtone, and Combination Bands: 2-Chloropropionitrile and α-Pinene.In-source reduction of the azo group during matrix-assisted laser desorption/ionization time-of-flight mass spectrometry experimentsAcridin-9-yl exchange: a proposal for the action of some 9-aminoacridine drugsThree types of induced tryptophan optical activity compared in model dipeptides: theory and experimentQuinacrine reactivity with prion proteins and prion-derived peptidesTheoretical Modeling of the Surface-Enhanced Raman Optical ActivityUnderstanding CH-Stretching Raman Optical Activity in Ala-Ala Dipeptides
P50
Q31021827-2137A797-D0C9-474A-84D8-FBCFE6B6E458Q33234693-50E6C59D-A900-44B9-A3AB-E4E8114B4EECQ33306559-305FB657-9540-4696-9F85-336541AAE583Q33315437-6E06EB99-802B-47B2-BFC5-3E8FC7E68339Q33740696-7084BA38-A7CF-42BC-812D-5153EEF8EB50Q34747474-4E960223-5DCE-4ADE-BAF1-DA3B65DF340DQ35992112-3FDD2CA0-0F6D-49AE-A69E-6330F5176940Q36107349-C3EA8F40-26F5-42E7-878F-E71C1CA21B3FQ36273059-E9BA4D59-5095-4140-BD37-E574AB4ED78DQ38315415-680210DA-57CF-43EF-9970-D7DFD5348B34Q39367777-C45C5977-8972-4B76-B533-CA3F13A877F0Q39633652-C291C370-8A3C-4664-9968-0DC93C403A58Q40229836-7CCF9990-1459-4901-91EB-E218C03AEE62Q45058132-9E586127-D963-4D82-826A-5E437BCCCF35Q45968906-EFA54477-9CA0-4AE2-BEFD-FA6344D878F4Q46210587-9C21D392-5F2A-4398-B8FA-442249B1DC3CQ46826316-F8ED62AC-AC56-4CBB-970D-3747795ED467Q48044322-3E6B4EDB-4CE8-4667-89DB-16606BC8CB67Q50228928-39327B21-2647-43BC-91B8-96145C18735FQ50892006-32C7824F-064E-4B3B-906F-24822CFEFB3CQ51277578-9B3040AF-28DB-4F2D-99EF-EBA13530F35BQ52321106-6BB5B5A1-30DC-4744-BB81-2FB669EFC48FQ53449364-9CCE8301-C1B2-4E3D-9161-C95CD48FEA24Q56933230-9646E560-6A34-46C1-B9C3-E3337CFABA8DQ57162962-9511F52F-15BC-4070-8BCC-AA4A97525129Q59613402-FCB2147D-70E8-4012-803B-E4E0F5B26065Q64938408-9DBAF46D-7F88-4D7C-B8F0-EF6C421F61F9Q79722192-6B3271AB-13EE-4802-93BB-3F3FEF8FC941Q80168454-EB4B40BC-FD50-40BB-8FE2-5DA0D5CF719AQ84394790-408E693C-F84F-44CE-8B6B-9D04ECAA891EQ85936852-83690ED4-DB58-40BB-9A3C-1BD1E2AAB4F7Q86761485-A6BABF9D-750A-4B88-9A48-8D606485221DQ92436782-AFEC88FF-064A-4808-8399-2E2252B55878
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jaroslav Sebestík
@ast
Jaroslav Sebestík
@en
Jaroslav Sebestík
@nl
Jaroslav Sebestík
@sl
type
label
Jaroslav Sebestík
@ast
Jaroslav Sebestík
@en
Jaroslav Sebestík
@nl
Jaroslav Sebestík
@sl
prefLabel
Jaroslav Sebestík
@ast
Jaroslav Sebestík
@en
Jaroslav Sebestík
@nl
Jaroslav Sebestík
@sl
P1053
C-9166-2012
P106
P1153
6506076468
P21
P31
P3829
P496
0000-0002-0614-2064