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phenylalanine amide

Known as: (S)-alpha-aminobenzenepropanamide, PheNH2 
National Institutes of Health

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Phenylalanine
analogs & derivatives

Papers overview

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2009
2009
Structure activity of C-terminal modified analogs of Ac-CCK-7.
Previous work indicates that both the C-terminal phenylalanine amide and the tryptophan moieties of cholecystokinin (CCK) are… 
2006
2006
Comparative assessment of two indices of drug induced permeability changes in the perfused rat intestine.
2004
2004
Synthesis of some derivatives of the C-terminal tetrapeptide of the hormone gastrin
SummaryThe synthesis has been effected of the C-terminal tetrapeptide of gastrin Trp · Met · Asp · PheNH2 · HCl (I) and its… 
1993
1993
Selective on-line enrichment and separation of peptides having aromatic amino acids at their C-termini by column-switching high-performance liquid chromatography using an anhydrochymotrypsin…
1993
1993
Inhibitor profile of porcine aminopeptidase W.
Aminopeptidase W (APW; EC 3.4.1 I . 16) belongs to the family of mammalian cell-surface zinc metallopeptidases [ 13. These… 
1991
1991
Determination of various molecular forms of cholecystokinin from canine mucosa by radioimmunoassay and bioassay.
Bioassays using amylase release from isolated pancreatic acini measure only cholecystokinin (CCK) forms with an intact carboxyl… 
1988
1988
[Stimulating action of polyphosphates on peptide formation from glycine and phenylalanine amides under abiogenic conditions].
Synthesis of peptides during polymerization of GlyNH2 and PheNH2 has been demonstrated by means of gel-chromatography and thin… 
1985
1985
Use of perdeuterated peptides in NMR studies of neurophysin-hormone interaction: demonstration of peptide-specific changes in neurophysin resonances.
1983
1983
Studies on angiotensin-converting enzyme inhibitors. I. Syntheses and angiotensin-converting enzyme inhibitory activity of 2-(3-mercaptopropionyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid…
(3S)-2-[(2S)-3-Mercapto-2-methylpropionyl]-1, 2, 3, 4-tetrahydroisoquinoline-3-carboxylic acid [(3S), (2S)-6a] was prepared by… 
1969
1969
Enzymatic inactivation of peptide hormones possessing a C-terminal amide group.
A partially purified enzyme extracted from the bladder of the toad, Bufo marinus L., was found to cleave the glycine amide moiety… 
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