European Journal of Endocrinology · 1973 · 14 citations · 3 references
Life SciencesBiochemistryEndocrinologyHormone BiochemistrySteroid BiochemistryStructure-activity RelationshipsAdrenal Steroid HormonesEnzyme InhibitionPeptide ChemistryPeptide Hormone BiochemistrySteroid Hormone BiochemistryArginine-rich PeptidesBiological Activity FeaturesLipolytic EnzymesPeptide Structure - Activity RelationshipsPeptide Structure-activity RelationshipsPositionSubstituent Effects On Biological Activity
ABSTRACT The steroidogenic and lipolytic activities of corticotrophin-(1–24)-tetracosapeptide and [Lys 17,18 ]corticotrophin-(1-18)-octadecapeptide amide were compared with those of the corresponding analogues variously substituted in position 8 with homo-arginine, ornithine or lysine. Peptides substituted with homo-arginine showed a surprisingly high degree of biological activity; in all the tests performed, the loss of activity due to the substitution did not exceed a factor of 3 to 10, while peptides substituted with ornithine or lysine in position 8 only showed residual biological activity or none at all, depending on the test system used. The results reported demonstrated that the presence of a guanidino group (arginine or homo-arginine side chain) in position 8 of the ACTH peptide is essential for the preservation of a high level of biological activity; the length of the aliphatic chain carrying the guanidino group is of minor importance.
3
Commission on Biochemical Nomenclature
Organon Scientific · 1987 · 422 citations
E J ROSS, George W. Thorn · The Medical Journal of Australia · 1935 · 17 citations