Add to ORKGThe solid phase procedure, based on the Fmoc (9-fluorenylmethyloxycarbonyl) chemistry, was used to prepare some peptide T analogues in which D-glucopyranosyl units are beta-O-glycosidically linked to Thr4 and/or Thr5 side chains. All glycopeptides showed significant human monocyte chemotaxis and high resistance to degradation by plasma or brain enzymes
The glycopeptide antibiotics are an important class of complex, medically relevant peptide natural p...
A series of UDP-disaccharide peptide compounds were synthesized as synthetic substrate analogues or ...
Glycosylation of proteins is the most complex form of posttranslational modification. Glycan chains ...
Four Major Histocompatibility Complex (MHC) Class I binding glycopeptides and two peptide analogues,...
The synthesis of a series of N-9-fluorenylmethoxycarbonyl (N-FMOC) protected amino acid glycosides i...
Linear and head to tail cyclic hexapeptide analogs (Xaa-Thr-Thr-Asn-Tyr-Thr, Xaa = D-Asp or D-iso-As...
A C-linked isostere of beta-D-galactosylated hydroxynorvaline has been prepared in eight steps from ...
Acquired immunodeficiency syndrome (AIDS) is initiated by the attachment of the human immunodeficien...
Protein glycosylation is a key post-translational modification important to many facets of biology. ...
Over the past few years, synthetic methods for the preparation of complex glycopeptides have been dr...
Fmoc-N,N'-Bis-Boc-7-guanyl-Tic-OH (GTIC), a conformationally constrained amino acid with basic prope...
In recent years, the conjugation of sugar moieties and lipoamino acids has been extensively investig...
The solid phase procedure, based on the Fmoc chemistry, was used to prepare some opioid deltorphin (...
O-glycopeptide analogues of enkephalin: FMOC-amino acid glycoside synthesis, solid-phase glycopeptid...
Using the potent cyclic peptide T analog [formula: see text] as parent compound, a series of analogu...
The glycopeptide antibiotics are an important class of complex, medically relevant peptide natural p...
A series of UDP-disaccharide peptide compounds were synthesized as synthetic substrate analogues or ...
Glycosylation of proteins is the most complex form of posttranslational modification. Glycan chains ...
Four Major Histocompatibility Complex (MHC) Class I binding glycopeptides and two peptide analogues,...
The synthesis of a series of N-9-fluorenylmethoxycarbonyl (N-FMOC) protected amino acid glycosides i...
Linear and head to tail cyclic hexapeptide analogs (Xaa-Thr-Thr-Asn-Tyr-Thr, Xaa = D-Asp or D-iso-As...
A C-linked isostere of beta-D-galactosylated hydroxynorvaline has been prepared in eight steps from ...
Acquired immunodeficiency syndrome (AIDS) is initiated by the attachment of the human immunodeficien...
Protein glycosylation is a key post-translational modification important to many facets of biology. ...
Over the past few years, synthetic methods for the preparation of complex glycopeptides have been dr...
Fmoc-N,N'-Bis-Boc-7-guanyl-Tic-OH (GTIC), a conformationally constrained amino acid with basic prope...
In recent years, the conjugation of sugar moieties and lipoamino acids has been extensively investig...
The solid phase procedure, based on the Fmoc chemistry, was used to prepare some opioid deltorphin (...
O-glycopeptide analogues of enkephalin: FMOC-amino acid glycoside synthesis, solid-phase glycopeptid...
Using the potent cyclic peptide T analog [formula: see text] as parent compound, a series of analogu...
The glycopeptide antibiotics are an important class of complex, medically relevant peptide natural p...
A series of UDP-disaccharide peptide compounds were synthesized as synthetic substrate analogues or ...
Glycosylation of proteins is the most complex form of posttranslational modification. Glycan chains ...