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NPC 14686

Known as: Fmoc-L-homophenylalanine, NPC-14686, NPC14686 
National Institutes of Health

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Related topics

1 relation

Broader (1)

Aminobutyrates

Papers overview

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2013
2013
Identification of Homophenylalanine Biosynthetic Genes from the Cyanobacterium Nostoc punctiforme PCC73102 and Application to Its Microbial Production by Escherichia coli
ABSTRACT l-Homophenylalanine (l-Hph) is a useful chiral building block for synthesis of several drugs, including angiotensin… 
Highly Cited
2009
Highly Cited
2009
Simultaneous synthesis of 2‐phenylethanol and L‐homophenylalanine using aromatic transaminase with yeast Ehrlich pathway
2‐Phenylethanol is a widely used aroma compound with rose‐like fragrance and L‐homophenylalanine is a building block of… 
Review
2009
Review
2009
Sustainable biocatalytic synthesis of L-homophenylalanine as pharmaceutical drug precursor.
2008
2008
Asymmetrical Synthesis of l‐Homophenylalanine Using Engineered Escherichia coli Aspartate Aminotransferase
Site‐directed mutagenesis was performed to change the substrate specificity of Escherichia coli aspartate aminotransferase (AAT… 
2008
2008
A novel hydantoinase process using recombinant Escherichia coli cells with dihydropyrimidinase and L-N-carbamoylase activities as biocatalyst for the production of L-homophenylalanine.
2006
2006
Enantioselective Synthesis of l‐Homophenylalanine by Whole Cells of Recombinant Escherichia coli Expressing l‐Aminoacylase and N‐Acylamino Acid Racemase Genes from Deinococcus radiodurans BCRC12827
l‐Homophenylalanine (l‐HPA) is a chiral unnatural amino acid used in the synthesis of angiotensin converting enzyme inhibitors… 
Highly Cited
2003
Highly Cited
2003
Asymmetric synthesis of L-homophenylalanine by equilibrium-shift using recombinant aromatic L-amino acid transaminase.
L-Homophenylalanine (L-HPA) was asymmetrically synthesized from 2-oxo-4-phenylbutyric acid (2-OPBA) and L-aspartate using a… 
2002
2002
Dipeptidyl peptidase I: importance of progranzyme activation sequences, other dipeptide sequences, and the N-terminal amino group of synthetic substrates for enzyme activity.
Highly Cited
1993
Highly Cited
1993
Inhibition of a Plasmodium vinckei cysteine proteinase cures murine malaria.
Intraerythrocytic malaria parasites degrade hemoglobin as a principal source of amino acids for parasite protein synthesis. We… 
Highly Cited
1991
Highly Cited
1991
Conformational restriction of the phenylalanine residue in a cyclic opioid peptide analogue: effects on receptor selectivity and stereospecificity.
In an effort to determine the effect of side chain conformational restriction on opioid receptor selectivity, the cyclic… 
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