Structure-activity relationships of cyclic and linear peptide T analogues

Int J Pept Protein Res. 1993 May;41(5):447-54. doi: 10.1111/j.1399-3011.1993.tb00464.x.

Abstract

Using the potent cyclic peptide T analog [formula: see text] as parent compound, a series of analogues were synthesized and their potencies in a monocyte chemotaxis assay were compared with those of correspondingly modified linear peptides. Structure-activity relationships observed with cyclic compounds did not always parallel those determined with linear analogues. [formula: see text] showed the highest affinity to CD4 receptor of monocytes of any peptide thus far studied. It also proved to be highly resistant to degradation by plasma or brain enzymes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Blood / metabolism
  • Brain / metabolism
  • CD4 Antigens / metabolism
  • Chemotaxis, Leukocyte / drug effects*
  • Dose-Response Relationship, Drug
  • Humans
  • Molecular Sequence Data
  • Monocytes / drug effects
  • Peptide T / analogs & derivatives
  • Peptide T / metabolism
  • Peptide T / pharmacology*
  • Peptides, Cyclic / chemistry
  • Peptides, Cyclic / pharmacology*
  • Structure-Activity Relationship

Substances

  • CD4 Antigens
  • Peptides, Cyclic
  • Peptide T