about
Conformational restriction through C alpha i C alpha i cyclization: Ac12c, the largest cycloaliphatic C alpha,alpha- disubstituted glycine knownEnergy transport in peptide helicesCIDEP effects of intramolecular quenching of singlet and triplet excited states by nitroxide radicals in oligopeptides: a potentially useful new method for investigating peptide secondary structures in solution.(+)-syn-Benzotriborneol an enantiopure C3-symmetric receptor for water.Trichogin: a paradigm for lipopeptaibols.Molecular spacers for physicochemical investigations based on novel helical and extended peptide structures.Peptide helices based on alpha-amino acids.Handedness preference and switching of peptide helices. Part I: Helices based on protein amino acids.Handedness preference and switching of peptide helices. Part II: Helices based on noncoded α-amino acids.Endothioxopeptides: A conformational overview.New naphthoquinone derivatives against glioma cells.Intramolecular backbone···backbone hydrogen bonds in polypeptide conformations. The other way around: ɛ-turn.En route towards the peptide γ-helix: X-ray diffraction analyses and conformational energy calculations of Adm-rich short peptides.Rational design of gold(III)-dithiocarbamato peptidomimetics for the targeted anticancer chemotherapy.Peptide-based rotaxanes and catenanes: an emerging class of supramolecular chemistry systems.Peptide δ-Turn: Literature Survey and Recent Progress.Structures of peptides from alpha-amino acids methylated at the alpha-carbon.A new tool for photoaffinity labeling studies: a partially constrained, benzophenone based, alpha-amino acid.Dynamical transition in a small helical peptide and its implication for vibrational energy transport.Vibrational energy transport in peptide helices after excitation of C-D modes in Leu-d10.Ac10c: a medium-ring, cycloaliphatic Calpha,alpha-disubstituted glycine. Incorporation into model peptides and preferred conformation.The crystal structure of the 1:1 inclusion complex of beta-cyclodextrin with squaric acid.Disaccharide modulation of the mitochondrial membrane fluidity changes induced by the membrane potential.Partial [alphaMe]Aun scan of [l-Leu11-OMe]-trichogin GA IV, a membrane active synthetic precursor of the natural lipopeptaibol.Structural versatility of peptides containing C alpha, alpha-dialkylated glycines. An X-ray diffraction study of six 1-aminocyclopropane-1-carboxylic acid rich peptides.C(alpha)-hydroxymethyl methionine: synthesis, optical resolution and crystal structure of its (+)-N(alpha)-benzoyl derivative.Nitroxyl peptides as catalysts of enantioselective oxidations.Probing structural requirements of fMLP receptor: on the size of the hydrophobic pocket corresponding to residue 2 of the tripeptide.Synthesis, conformational analysis, and spectroscopic characterization of peptides based on Daf, the first rigid transition-metal receptor, cyclic C(alpha,alpha)-disubstituted glycine.Reactive intermediates in peptide synthesis. ortho-Nitrophenyl Nalpha-para-toluenesulfonyl-alpha-aminoisobutyrate.Reactive intermediates in peptide synthesis: the N-oxysuccinimido ester of Nalpha-para-toluenesulfonyl-alpha-aminoisobutyric acid.Peptoid residues and beta-turn formation.Pseudopeptide foldamers: the homo-oligomers of pyroglutamic acid.Multiple, consecutive, fully-extended 2.0₅-helix peptide conformation.Insights into the free-energy dependence of intramolecular dissociative electron transfers.Studies of peptides forming 3(10)- and alpha-helices and beta-bend ribbon structures in organic solution and in model biomembranes by Fourier transform infrared spectroscopy.Zinc(II) as an allosteric regulator of liposomal membrane permeability induced by synthetic template-assembled tripodal polypeptides.Folding of peptides characterized by c3Val, a highly constrained analogue of valine.Structural modifications of the permeability transition pore complex in resealed mitochondria induced by matrix-entrapped disaccharides.N-benzhydryl-glycolamide: the first protecting group in peptide synthesis with a strong conformational bias.
P50
Q28370640-905E5F8F-9FA9-43DD-8BDA-E0966A7A141FQ30479840-A3507235-3173-4234-AC4B-E8D20A11B937Q30924433-4A21A3DA-ECD6-4F6F-84C5-9D69D263589DQ34164332-AFD4CA02-AA1E-4C35-BE24-FFD867BEEB01Q35601457-5D218E50-52FD-490E-A476-B5C18D907100Q35726691-46B2EF9A-1C99-4552-92C7-A93B4B470EE4Q36241364-24C0AE7C-5A2D-4DEF-B662-28B0B8E79F0DQ38206760-1E769F4B-AC0C-4693-835B-A3C22A4E6283Q38340034-C0F6CF7C-04B0-42E9-B002-CC47BF9D850DQ38880136-A7714F9A-D999-46F9-8051-03E1B2C287BFQ38881820-722C433D-2A4D-453D-94DA-C043A6B30DDEQ38893938-2267FCB2-2FE6-4861-8631-F2455C37414FQ39075913-A091951C-F754-4A47-9090-50A4EEDD9D98Q39300146-8BD7EEE0-4EE6-46B5-A2CD-10392811C2AAQ39634589-5C0E3E3B-55A8-4B6C-A1FF-45BC3D1A01E4Q40659418-54E51678-5595-41AF-9EAF-71C1CA1BBD3AQ40831000-C087DF79-BCA6-4446-8D13-2A6CB7152FE4Q43053340-2917A6E5-6ADB-4360-BF04-BDAF5E017763Q43276646-4EF27860-D493-4FA7-B96E-3D3C7EDA8620Q43276656-4FD8753E-6D68-42CF-9F5A-2426CE634B77Q43591994-7BDCCAFE-762E-4D84-A332-A17CEEFFED60Q43670670-6C8CF54B-8AD1-4C21-815C-4DFD8DCE12ABQ43681465-2DB7340A-00EB-4B56-8E4F-F8FA468B33ECQ43770160-CDD7B144-D881-4578-92E3-467B6F813B7EQ43783992-A4B945E9-E2D3-4B2B-925B-E711B0C109E8Q43858744-7857DEF8-15A2-4D7C-872D-0966E3D36836Q43873375-6D487FAD-E855-426D-BB12-9AF80ECD1EC3Q43892192-B7802E9B-4F5C-4E3B-97F7-96C6C6E0A07AQ43904939-6FCD759B-5335-4F32-B67D-5D2C3F62BEFCQ43947119-93ADA87E-3F87-4E60-B550-52E524E06A3FQ43976378-F34DDD13-76D1-4A8F-8E80-275C983DA2F2Q44046870-C1509DE4-3143-4164-9443-B3874C344CEEQ44103233-9240564C-505E-4F6D-8989-0C14A274F7CAQ44117329-59DDAA23-6CAB-47E6-85CB-06373F3F1533Q44140467-602F0EE3-A748-4A28-BD90-2EB1DAB01075Q44150638-2AED16AF-9EBD-4584-AA78-BC5146913F9EQ44188054-27E963D0-3AB0-46C0-8741-86C92084B7C5Q44291830-81D63253-959B-4F04-A426-449C4DC0F03AQ44298071-BB5A14F1-C0C0-49D0-AE82-C963D79908C1Q44415324-EEB3BC79-1561-403D-A10A-F3E637C31381
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Marco Crisma
@ast
Marco Crisma
@en
Marco Crisma
@es
Marco Crisma
@nl
Marco Crisma
@sl
type
label
Marco Crisma
@ast
Marco Crisma
@en
Marco Crisma
@es
Marco Crisma
@nl
Marco Crisma
@sl
prefLabel
Marco Crisma
@ast
Marco Crisma
@en
Marco Crisma
@es
Marco Crisma
@nl
Marco Crisma
@sl
P1053
K-6626-2013
P106
P1153
7005328233
P21
P31
P3829
P496
0000-0003-3552-4106