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N‐Terminal Cu‐Binding Motifs (Xxx‐Zzz‐His, Xxx‐His) and Their Derivatives: Chemistry, Biology and Medicinal Applications
N‐Terminal Cu‐Binding Motifs (Xxx‐Zzz‐His, Xxx‐His) and Their Derivatives: Chemistry, Biology and Medicinal Applications
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N‐Terminal Cu‐Binding Motifs (Xxx‐Zzz‐His, Xxx‐His) and Their Derivatives: Chemistry, Biology and Medicinal Applications

Gonzalez, Paulina ; Bossak, Karolina ; Stefaniak, Ewelina ; Hureau, Christelle ; Raibaut, Laurent ; Bal, Wojciech ; Faller, Peter

Chemistry : a European journal, 2018-06, Vol.24 (32), p.8029-8041 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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Frontispiece: N‐Terminal Cu‐Binding Motifs (Xxx‐Zzz‐His, Xxx‐His) and Their Derivatives: Chemistry, Biology and Medicinal Applications
Frontispiece: N‐Terminal Cu‐Binding Motifs (Xxx‐Zzz‐His, Xxx‐His) and Their Derivatives: Chemistry, Biology and Medicinal Applications
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Frontispiece: N‐Terminal Cu‐Binding Motifs (Xxx‐Zzz‐His, Xxx‐His) and Their Derivatives: Chemistry, Biology and Medicinal Applications

Gonzalez, Paulina ; Bossak, Karolina ; Stefaniak, Ewelina ; Hureau, Christelle ; Raibaut, Laurent ; Bal, Wojciech ; Faller, Peter

Chemistry : a European journal, 2018-06, Vol.24 (32), p.n/a [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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3
Towards Understanding the Tandem Mass Spectra of Protonated Oligopeptides. 2: The Proline Effect in Collision-Induced Dissociation of Protonated Ala-Ala-Xxx-Pro-Ala (Xxx = Ala, Ser, Leu, Val, Phe, and Trp)
Towards Understanding the Tandem Mass Spectra of Protonated Oligopeptides. 2: The Proline Effect in Collision-Induced Dissociation of Protonated Ala-Ala-Xxx-Pro-Ala (Xxx = Ala, Ser, Leu, Val, Phe, and Trp)
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Towards Understanding the Tandem Mass Spectra of Protonated Oligopeptides. 2: The Proline Effect in Collision-Induced Dissociation of Protonated Ala-Ala-Xxx-Pro-Ala (Xxx = Ala, Ser, Leu, Val, Phe, and Trp)

Bleiholder, Christian ; Suhai, Sándor ; Harrison, Alex G. ; Paizs, Béla

Journal of the American Society for Mass Spectrometry, 2011-06, Vol.22 (6), p.1032-1039 [Periódico revisado por pares]

New York: Springer-Verlag

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4
Kinetic deconjugation: a gateway to the synthesis of Xxx-Gly (E)-alkene dipeptide isosteres
Kinetic deconjugation: a gateway to the synthesis of Xxx-Gly (E)-alkene dipeptide isosteres
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Kinetic deconjugation: a gateway to the synthesis of Xxx-Gly (E)-alkene dipeptide isosteres

Proteau-Gagné, Arnaud ; Nadon, Jean-François ; Bernard, Sylvain ; Guérin, Brigitte ; Gendron, Louis ; Dory, Yves L.

Tetrahedron letters, 2011-12, Vol.52 (49), p.6603-6605 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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5
Galectin-1-Asialofetuin Interaction Is Inhibited by Peptides Containing the Tyr-Xxx-Tyr Motif Acting on the Glycoprotein
Galectin-1-Asialofetuin Interaction Is Inhibited by Peptides Containing the Tyr-Xxx-Tyr Motif Acting on the Glycoprotein
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Galectin-1-Asialofetuin Interaction Is Inhibited by Peptides Containing the Tyr-Xxx-Tyr Motif Acting on the Glycoprotein

Wéber, Edit ; Hetényi, Anasztázia ; Váczi, Balázs ; Szolnoki, Éva ; Fajka-Boja, Roberta ; Tubak, Vilmos ; Monostori, Éva ; Martinek, Tamás A

Chembiochem : a European journal of chemical biology, 2010-01, Vol.11 (2), p.228-234 [Periódico revisado por pares]

Weinheim: Wiley-VCH Verlag

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6
A Short Synthesis of Bicyclic Dipeptides Corresponding to Xxx-l-Pro Xxx-d-Pro Having Constrained trans-Proline Amides
A Short Synthesis of Bicyclic Dipeptides Corresponding to Xxx-l-Pro Xxx-d-Pro Having Constrained trans-Proline Amides
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A Short Synthesis of Bicyclic Dipeptides Corresponding to Xxx-l-Pro Xxx-d-Pro Having Constrained trans-Proline Amides

Curran, Timothy P ; Marcaurelle, Lisa A ; O'Sullivan, Kathleen M

Organic letters, 1999-10, Vol.1 (8), p.1225-1228 [Periódico revisado por pares]

United States: American Chemical Society

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7
Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals
Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals
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Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals

Antimonova, A. N. ; Petrenko, N. I. ; Shults, E. E. ; Polienko, Yu. F. ; Shakirov, M. M. ; Irtegova, I. G. ; Pokrovskii, M. A. ; Sherman, K. M. ; Grigor’ev, I. A. ; Pokrovskii, A. G. ; Tolstikov, G. A.

Russian journal of bioorganic chemistry, 2013-03, Vol.39 (2), p.181-185 [Periódico revisado por pares]

Dordrecht: SP MAIK Nauka/Interperiodica

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8
ExoMars Mars Organic Molecule Analyzer (MOMA) Laser Desorption/Ionization Mass Spectrometry (LDI-MS) Analysis of Phototrophic Communities from a Silica-Depositing Hot Spring in Yellowstone National Park, USA
ExoMars Mars Organic Molecule Analyzer (MOMA) Laser Desorption/Ionization Mass Spectrometry (LDI-MS) Analysis of Phototrophic Communities from a Silica-Depositing Hot Spring in Yellowstone National Park, USA
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ExoMars Mars Organic Molecule Analyzer (MOMA) Laser Desorption/Ionization Mass Spectrometry (LDI-MS) Analysis of Phototrophic Communities from a Silica-Depositing Hot Spring in Yellowstone National Park, USA

Siljeström, Sandra ; Li, Xiang ; Brinckerhoff, William ; van Amerom, Friso ; Cady, Sherry L

Astrobiology, 2021-12, Vol.21 (12), p.1515-1525 [Periódico revisado por pares]

United States: Mary Ann Liebert, Inc

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9
A short synthesis of bicyclic dipeptides corresponding to Xxx-L-Pro and Xxx-D-Pro having constrained cis-proline amides
A short synthesis of bicyclic dipeptides corresponding to Xxx-L-Pro and Xxx-D-Pro having constrained cis-proline amides
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A short synthesis of bicyclic dipeptides corresponding to Xxx-L-Pro and Xxx-D-Pro having constrained cis-proline amides

Curran, Timothy P ; McEnaney, Patrick M

Tetrahedron letters, 1995-01, Vol.36 (2), p.191-194 [Periódico revisado por pares]

Elsevier Ltd

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10
Arene complexes of transition metals in reactions with nucleophilic reagents: XXX. Reaction of π-halomesitylene [Tetramethyl(ethyl)cyclopentadienyl]rhodium(II) complexes with anions derived from CH acids
Arene complexes of transition metals in reactions with nucleophilic reagents: XXX. Reaction of π-halomesitylene [Tetramethyl(ethyl)cyclopentadienyl]rhodium(II) complexes with anions derived from CH acids
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Arene complexes of transition metals in reactions with nucleophilic reagents: XXX. Reaction of π-halomesitylene [Tetramethyl(ethyl)cyclopentadienyl]rhodium(II) complexes with anions derived from CH acids

Goryunov, L. I. ; Romanova, N. M. ; Zhilovskii, G. S. ; Shteingarts, V. D.

Russian journal of organic chemistry, 2007-12, Vol.43 (12), p.1765-1772 [Periódico revisado por pares]

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