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NPC 14686
Known as:
Fmoc-L-homophenylalanine
, NPC-14686
, NPC14686
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
Aminobutyrates
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Formation of Benzyl Carbanion in Collision-Induced Dissociation of Deprotonated Phenylalanine Homologues.
K. Sekimoto
,
Natsuki Matsuda
,
M. Takayama
Mass Spectrometry
2014
Corpus ID: 11094499
The fragmentation behavior of deprotonated L-phenylalanine (Phe) and its homologues including L-homophenylalanine (HPA) and L…
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2014
2014
The mechanism of NPC-14686-induced [Ca²⁺]i rises and non-Ca²⁺-triggered cell death in MG63 human osteosarcoma cells.
J. Chien
,
C. Chou
,
+5 authors
C. Jan
Chinese journal of physiology
2014
Corpus ID: 21148439
NPC-14686 has been shown to have anti-inflammatory effect in previous studies, but the mechanisms are unclear. The effect of NPC…
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2009
2009
Asymmetrically simultaneous synthesis of L‐homophenylalanine and N6‐protected‐2‐oxo‐6‐amino‐hexanoic acid by engineered Escherichia coli aspartate aminotransferase
H. Lo
,
Wei-De Lin
,
S. Hsu
,
W. Hsu
Biotechnology progress (Print)
2009
Corpus ID: 32995196
L‐Homophenylalanine (L‐HPA) and N6‐protected‐2‐oxo‐6‐amino‐hexanoic acid (N6‐protected‐OAHA) can be used as building blocks for…
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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.
Chao-Hung Kao
,
H. Lo
,
S. Hsu
,
W. Hsu
Journal of Biotechnology
2008
Corpus ID: 205738514
2007
2007
Highly Potent and Selective Substrate Analogue Factor Xa Inhibitors Containing D‐Homophenylalanine Analogues as P3 Residue: Part 2
A. Stürzebecher
,
Daniel Doennecke
,
+7 authors
T. Steinmetzer
ChemMedChem
2007
Corpus ID: 9186189
A series of highly potent substrate‐analogue factor Xa inhibitors containing D‐homophenylalanine analogues as the P3 residue has…
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2003
2003
Effect of NPC-14686 (Fmoc-L-homophenylalanine) on intracellular Ca2+ levels in human hepatoma cells.
C. Jan
,
S. Kuo
,
Jin‐shiung Cheng
,
Y. Lo
,
Chun‐Peng Liu
,
Wei-Chung Chen
Life Science
2003
Corpus ID: 27011770
2000
2000
NPC-14686, a novel anti-inflammatory agent, increased intracellular Ca(2+) concentrations in MDCK renal tubular cells.
C. Jan
,
J. L. Wang
,
+6 authors
J. K. Huang
International Journal of Immunopharmacology
2000
Corpus ID: 25223192
Highly Cited
1993
Highly Cited
1993
Inhibition of a Plasmodium vinckei cysteine proteinase cures murine malaria.
Philip J. Rosenthal
,
G. K. Lee
,
R. E. Smith
Journal of Clinical Investigation
1993
Corpus ID: 22125005
Intraerythrocytic malaria parasites degrade hemoglobin as a principal source of amino acids for parasite protein synthesis. We…
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Highly Cited
1991
Highly Cited
1991
Conformational restriction of the phenylalanine residue in a cyclic opioid peptide analogue: effects on receptor selectivity and stereospecificity.
P. Schiller
,
G. Weltrowska
,
+4 authors
B. Wilkes
Journal of Medicinal Chemistry
1991
Corpus ID: 43186504
In an effort to determine the effect of side chain conformational restriction on opioid receptor selectivity, the cyclic…
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1990
1990
Mechanism of binding of substrate analogues to tryptophan indole-lyase: studies using rapid-scanning and single-wavelength stopped-flow spectrophotometry.
R. S. Phillips
,
Sheri L. Bender
,
P. Brzovic
,
Michael F. Dunn
Biochemistry
1990
Corpus ID: 20779280
We have examined the binding of oxindolyl-L-alanine, (3R)-2,3-dihydro-L-tryptophan, L-homophenylalanine, and N1-methyl-L…
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