P1751

D-Phenylalanine

≥98% (HPLC)

• Synonyme(s) : (R)-2-Amino-3-phenylpropionic acid
• Formule empirique (notation de Hill) : C₉H₁₁NO₂
• Numéro CAS: 673-06-3
• Poids moléculaire : 165.19
• NACRES: NA.26
• PubChem Substance ID: 24898241
• UNSPSC Code: 12352209
• EC Number: 211-603-5
• MDL number: MFCD00004270
• Beilstein/REAXYS Number: 2804068

Propriétés

• Nom du produit: D-Phenylalanine, ≥98% (HPLC)
• Quality Segment: 300
• 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)

Description

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>

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)