Hochschulschrift
Synthesis of conformationally restricted amino acids and their use in the preparation of biologically active peptides and peptidomimetics
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Sprache
-
Englisch
- Anmerkungen
-
Regensburg, Univ., Diss., 2008 und Milano, Univ., Diss., 2008
- Schlagwort
-
Naturstoff
Polymere
Makromolekulare Chemie
Makromolekül
- Urheber
-
Cattaneo, Cristian
- URN
-
urn:nbn:de:bvb:355-epub-133899
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:32 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Objekttyp
- Hochschulschrift
Beteiligte
- Cattaneo, Cristian
Ähnliche Objekte (12)
Preparation of Thioacid-Containing Amino Acids and Peptides and Their Application in Ligation Reactions
Interaction and aggregation mechanisms of peptides at biologically relevant interfaces
HLA-F*01:01-restricted peptides reveal to prefer a length of 16 amino acids with N-terminal flexibility
Computational studies of the interactions of biologically active peptides with membrane
Special issue Amino acids, peptides and proteins
Special issue Amino acids, peptides and proteins
Lecture 18. Amino Acids, Peptides, and Proteins.
β-amino [Beta-amino] acids as secondary structure inducers in peptides
Amino acids, peptides and proteins in organic chemistry, Vol. 5.. Analysis and function of amino acids and peptides
Engineering the genetic code and expanding the genetic code for in vivo incorporation of noncanonical amino acids into biologically active ribosomal peptides
Synthesis of conformationally restricted amino acids : highly versatile scaffolds
Synthesis of conformationally restricted amino acids : highly versatile scaffolds
Preparation of Thioacid-Containing Amino Acids and Peptides and Their Application in Ligation Reactions
Interaction and aggregation mechanisms of peptides at biologically relevant interfaces
HLA-F*01:01-restricted peptides reveal to prefer a length of 16 amino acids with N-terminal flexibility
Computational studies of the interactions of biologically active peptides with membrane
Special issue Amino acids, peptides and proteins
Special issue Amino acids, peptides and proteins
Lecture 18. Amino Acids, Peptides, and Proteins.
β-amino [Beta-amino] acids as secondary structure inducers in peptides
Amino acids, peptides and proteins in organic chemistry, Vol. 5.. Analysis and function of amino acids and peptides
Engineering the genetic code and expanding the genetic code for in vivo incorporation of noncanonical amino acids into biologically active ribosomal peptides
Synthesis of conformationally restricted amino acids : highly versatile scaffolds
Synthesis of conformationally restricted amino acids : highly versatile scaffolds
Preparation of Thioacid-Containing Amino Acids and Peptides and Their Application in Ligation Reactions
Interaction and aggregation mechanisms of peptides at biologically relevant interfaces
HLA-F*01:01-restricted peptides reveal to prefer a length of 16 amino acids with N-terminal flexibility
Computational studies of the interactions of biologically active peptides with membrane
Special issue Amino acids, peptides and proteins
Special issue Amino acids, peptides and proteins
Lecture 18. Amino Acids, Peptides, and Proteins.
β-amino [Beta-amino] acids as secondary structure inducers in peptides
Amino acids, peptides and proteins in organic chemistry, Vol. 5.. Analysis and function of amino acids and peptides
Engineering the genetic code and expanding the genetic code for in vivo incorporation of noncanonical amino acids into biologically active ribosomal peptides
Synthesis of conformationally restricted amino acids : highly versatile scaffolds