All Photos(4)
Synonym(s):
(R)-2-Amino-3-phenylpropionic acid
Empirical Formula (Hill Notation):
C9H11NO2
CAS Number:
Molecular Weight:
165.19
Beilstein:
2804068
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
Recommended Products
Quality Level
Assay
≥98% (HPLC)
form
powder
color
white to off-white
mp
273-276 °C
application(s)
cell analysis
SMILES string
N[C@H](Cc1ccccc1)C(O)=O
InChI
1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m1/s1
InChI key
COLNVLDHVKWLRT-MRVPVSSYSA-N
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Related Categories
Application
<ul>
<li><strong>Paper Title: </strong> Supramolecular nanofibers co-loaded with dabrafenib and doxorubicin for targeted and synergistic therapy of differentiated thyroid carcinoma. D-Phenylalanine are used to improve the stability of peptides <em>in vivo</em> (Chen P et al., 2023).</li>
<li><strong>Paper Title: </strong> Mechanistic aspects of the transamination reactions catalyzed by D-amino acid transaminase from Haliscomenobacter hydrossis. This study focuses on the enzymatic roles of D-Phenylalanine in specific bacterial transamination processes, applicable in biocatalysis and synthetic biology (Bakunova AK et al., 2023).</li>
</ul>
<li><strong>Paper Title: </strong> Supramolecular nanofibers co-loaded with dabrafenib and doxorubicin for targeted and synergistic therapy of differentiated thyroid carcinoma. D-Phenylalanine are used to improve the stability of peptides <em>in vivo</em> (Chen P et al., 2023).</li>
<li><strong>Paper Title: </strong> Mechanistic aspects of the transamination reactions catalyzed by D-amino acid transaminase from Haliscomenobacter hydrossis. This study focuses on the enzymatic roles of D-Phenylalanine in specific bacterial transamination processes, applicable in biocatalysis and synthetic biology (Bakunova AK et al., 2023).</li>
</ul>
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Gigantic vortical differential scattering as a monochromatic probe for multiscale chiral structures.
Jincheng Ni et al.
Proceedings of the National Academy of Sciences of the United States of America, 118(2) (2020-12-30)
Spin angular momentum of light is vital to investigate enantiomers characterized by circular dichroism (CD), widely adopted in biology, chemistry, and material science. However, to discriminate chiral materials with multiscale features, CD spectroscopy normally requires wavelength-swept laser sources as well
Andrew T Schuster et al.
Gastroenterology, 148(7), 1405-1416 (2015-02-24)
Defects in colonic epithelial barrier defenses are associated with ulcerative colitis (UC). The proteins that regulate bacterial clearance in the colonic epithelium have not been completely identified. The Drosophila chromosome-associated protein D3 (dCAP-D3) regulates responses to bacterial infection. We examined
Teresa Blazek et al.
Biosensors & bioelectronics, 163, 112260-112260 (2020-06-23)
The case study of four FAD-dependent oxidase enzymes is presented in the context of the often-claimed direct electron transfer (DET) to glucose oxidase at carbon nanotubes (CNT). The selected enzymes included d-amino acid (AAOx), alcohol (AOx), pyranose (PyOx), and choline
Suneela S Dhaneshwar et al.
European journal of medicinal chemistry, 44(1), 131-142 (2008-05-13)
Mutual amide prodrugs of 4-aminosalicylic acid with D-phenylalanine and L-tryptophan were synthesized for targeted drug delivery to the inflamed gut tissue in inflammatory bowel disease. Stability studies in aqueous buffers (pH 1.2 and 7.4) showed that the synthesized prodrugs were
Ruth Milkereit et al.
Nature communications, 6, 7250-7250 (2015-05-23)
Mammalian target of rapamycin 1 (mTORC1), a master regulator of cellular growth, is activated downstream of growth factors, energy signalling and intracellular essential amino acids (EAAs) such as Leu. mTORC1 activation occurs at the lysosomal membrane, and involves V-ATPase stimulation
Chromatograms
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