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F5126

Sigma-Aldrich

m-Fluoro-DL-phenylalanine

≥98%

Sinônimo(s):

3-Fluoro-DL-phenylalanine

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About This Item

Fórmula linear:
FC6H4CH2CH(NH2)COOH
Número CAS:
456-88-2
Peso molecular:
183.18
Beilstein:
2939807
Número CE:
220-104-1
Número MDL:
MFCD00004273
Código UNSPSC:
12352209
ID de substância PubChem:
24894882
NACRES:
NA.26

product name

m-Fluoro-DL-phenylalanine,

Ensaio

≥98%

forma

powder

cor

white to off-white

pf

240-250 °C

aplicação(ões)

cell analysis
peptide synthesis

cadeia de caracteres SMILES

NC(Cc1cccc(F)c1)C(O)=O

InChI

1S/C9H10FNO2/c10-7-3-1-2-6(4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)

chave InChI

VWHRYODZTDMVSS-UHFFFAOYSA-N

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Categorias relacionadas

Ações bioquímicas/fisiológicas

m-Fluoro-DL-phenylalanine, a toxic antimetabolite, is a racemic mixture of a substituted (halogenated) benzoyl D and L phenylalanine with potential use in antiviral and antimicrobial drug development.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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Nick J P Wierckx et al.
Applied and environmental microbiology, 71(12), 8221-8227 (2005-12-08)
Efficient bioconversion of glucose to phenol via the central metabolite tyrosine was achieved in the solvent-tolerant strain Pseudomonas putida S12. The tpl gene from Pantoea agglomerans, encoding tyrosine phenol lyase, was introduced into P. putida S12 to enable phenol production.
Monica N Kinde et al.
Proceedings of the National Academy of Sciences of the United States of America, 113(48), 13762-13767 (2016-11-20)
Voltage-gated sodium channels (NaV) play an important role in general anesthesia. Electrophysiology measurements suggest that volatile anesthetics such as isoflurane inhibit NaV by stabilizing the inactivated state or altering the inactivation kinetics. Recent computational studies suggested the existence of multiple
Julianne L Kitevski-LeBlanc et al.
Journal of biomolecular NMR, 48(2), 113-121 (2010-08-25)
In protein NMR experiments which employ nonnative labeling, incomplete enrichment is often associated with inhomogeneous line broadening due to the presence of multiple labeled species. We investigate the merits of fractional enrichment strategies using a monofluorinated phenylalanine species, where resolution
Julianne L Kitevski-Leblanc et al.
Journal of biomolecular NMR, 47(2), 113-123 (2010-04-20)
Traditional single site replacement mutations (in this case, phenylalanine to tyrosine) were compared with methods which exclusively employ (15)N and (19)F-edited two- and three-dimensional NMR experiments for purposes of assigning (19)F NMR resonances from calmodulin (CaM), biosynthetically labeled with 3-fluorophenylalanine
H Ito et al.
Agricultural and biological chemistry, 54(3), 699-705 (1990-03-01)
A wild-type parent of Brevibacterium lactofermentum was converted into an L-Tyr producer by three steps of genetic breeding. First, acquirement of m-fluoro-D, L-phenylalanine resistance (1,000 microgram/ml) brought about MF1317 which produced 3.5 g/l of L-Tyr and a byproduct of 2.8
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