A highly active chemotactic peptide analog incorporating the unusual residue 1-aminocyclohexanecarboxylic acid at position 2

Biochemical and Biophysical Research Communications

Volumn 128, Issue 1, 1985, Pages 339-344

  Sukumar, M ^a   Raj, P Antony ^a   Balaram, P ^a   Becker, E L ^b  

^a INDIAN INSTITUTE OF SCIENCE   (India)

^b UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1 AMINOCYCLOHEXANECARBOXYLIC ACID; 1-AMINOCYCLOHEXANECARBOXYLIC ACID; AMINO ACID; CYCLOHEXANECARBOXYLIC ACID DERIVATIVE; DRUG DERIVATIVE; FORMYLMETHIONYLLEUCYLPHENYLALANINE; LYSOZYME; N FORMYLMETHIONINE LEUCYL PHENYLALANINE;

ANIMAL; ARTICLE; BLOOD; DRUG EFFECT; ENZYMOLOGY; NEUTROPHIL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RABBIT; STRUCTURE ACTIVITY RELATION;

AMINO ACIDS; ANIMAL; CYCLOHEXANECARBOXYLIC ACIDS; MAGNETIC RESONANCE SPECTROSCOPY; MURAMIDASE; N-FORMYLMETHIONINE LEUCYL-PHENYLALANINE; NEUTROPHILS; RABBITS; STRUCTURE-ACTIVITY RELATIONSHIP; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0022427387     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/0006-291X(85)91684-5     Document Type: Article

References (13)

1. Conformational effects on peptide aggregation in organic solvents: spectroscopic studies of two chemotactic tripeptide analogs.
2. 1161. Peptides. Part XVIII. Derivatives of 1-aminocyclohexanecarboxylic acid