Product Data Sheet

L-Phenylalanine-13C9,15N,d8

Catalog No. A66222

main product photo
L-Phenylalanine-13C9,15N,d8 is a stable isotope-labeled form of L-Phenylalanine, featuring deuterium and carbon isotopes. As an essential amino acid, it plays a vital role in protein synthesis and is also recognized for its interaction with voltage-dependent Ca2+ channels, acting as an antagonist with a Ki of 980 nM. Additionally, L-Phenylalanine competitively antagonizes the glycine and glutamate-binding sites of N-methyl-D-aspartate receptors (NMDARs), with a KB of 573 μM. This compound is useful in biochemical research and applications involving metabolic studies, tracer applications, and drug development.
Chemical Information
Catalog NumA66222
M. Wt183.17
Formula13C9H3D815NO2
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.1994331-22-4
Synonyms(S)-2-Amino-3-phenylpropionic acid-13C9,15N,d8
SMILESO[13C]([13C@]([2H])([13C]([2H])([13C]1=[13C]([13C]([2H])=[13C]([13C]([2H])=[13C]1[2H])[2H])[2H])[2H])[15NH2])=O
Biological Activity
DescriptionL-Phenylalanine-13C9,15N,d8 is a stable isotope-labeled form of L-Phenylalanine, featuring deuterium and carbon isotopes. As an essential amino acid, it plays a vital role in protein synthesis and is also recognized for its interaction with voltage-dependent Ca2+ channels, acting as an antagonist with a Ki of 980 nM. Additionally, L-Phenylalanine competitively antagonizes the glycine and glutamate-binding sites of N-methyl-D-aspartate receptors (NMDARs), with a KB of 573 μM. This compound is useful in biochemical research and applications involving metabolic studies, tracer applications, and drug development.
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SHIPPING AND STORAGE
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