Skip to search formSkip to main contentSkip to account menu

butyloxycarbonyl-phenylalanyl-leucyl-phenylalanyl-leucyl-phenylalanine

Known as: N-t-Boc-Phe-Leu-Phe-Leu-Phe, butyloxycarbonyl-Phe-Leu-Phe-Leu-Phe, N-tertiary-butyloxycarbonyl-phenylalanyl-leucyl-phenylalanyl-leucyl-phenylalanine 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
1990
Highly Cited
1990
The effects of GDP and of aurodox (N-methylkirromycin) on the affinity of elongation factor Tu (EF-Tu) for aminoacyl-tRNA (aa… 
Highly Cited
1988
Highly Cited
1988
A series of renin inhibitors containing the dipeptide transition state mimics (2S,4S,5S)-5-amino-4-hydroxy-2-isopropyl-7… 
Highly Cited
1986
Highly Cited
1986
The binding affinities of tRNAPhe, Phe-tRNAPhe, and N-AcPhe-tRNAPhe from either Escherichia coli or yeast to the P, A, and E… 
Highly Cited
1985
Highly Cited
1985
Analogues of the renin octapeptide substrate were synthesized in which replacement of the scissile dipeptide with (3S,4S)-4-amino… 
Highly Cited
1984
Highly Cited
1984
The relationship between receptor binding of the formylated peptide chemoattractant formylmethionylleucylphenylalanine (fMet-Leu… 
Highly Cited
1981
Highly Cited
1981
Six analogues of substance P were synthesized with the aim of developing a metabolically stable peptide that would retain the… 
Highly Cited
1976
Highly Cited
1976
Codon-anticodon interaction induces an allosteric rearrangement of the three-dimensional structure of Phe-tRNAPhe that exposes…