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P1751

Sigma-Aldrich

D-Phenylalanine

≥98% (HPLC)

Sinónimos:

(R)-2-Amino-3-phenylpropionic acid

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About This Item

Fórmula empírica (notación de Hill):
C9H11NO2
Número de CAS:
673-06-3
Peso molecular:
165.19
Beilstein/REAXYS Number:
2804068
EC Number:
211-603-5
MDL number:
MFCD00004270
UNSPSC Code:
12352209
PubChem Substance ID:
24898241
NACRES:
NA.26

product name

D-Phenylalanine, ≥98% (HPLC)

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

Gene Information

human ... CA1(759) , CA14(23632) , CA2(760) , CA4(762) , CA5A(763) , CA7(766)

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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>

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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L-Phenylalanine certified reference material, TraceCERT&#174;, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

40541

L-Phenylalanine

D-Methionine &#8805;98% (HPLC)

Sigma-Aldrich

M9375

D-Methionine

D-Tryptophan &#8805;98.0% (HPLC)

Sigma-Aldrich

T9753

D-Tryptophan

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
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
Florian Beaumatin et al.
Molecular cell, 76(1), 163-176 (2019-09-08)
Sensing nutrient availability is essential for appropriate cellular growth, and mTORC1 is a major regulator of this process. Mechanisms causing mTORC1 activation are, however, complex and diverse. We report here an additional important step in the activation of mTORC1, which
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