89377
4-Fluoro-DL-glutamic acid
≥93%
Sinônimo(s):
(±)-2-Amino-4-fluoroglutaric acid
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About This Item
Fórmula empírica (Notação de Hill):
C5H8FNO4
Número CAS:
Peso molecular:
165.12
Beilstein:
5254612
Número CE:
Número MDL:
Código UNSPSC:
12352200
ID de substância PubChem:
Produtos recomendados
Ensaio
≥93%
Formulário
solid
aplicação(ões)
peptide synthesis
cadeia de caracteres SMILES
NC(CC(F)C(O)=O)C(O)=O
InChI
1S/C5H8FNO4/c6-2(4(8)9)1-3(7)5(10)11/h2-3H,1,7H2,(H,8,9)(H,10,11)
chave InChI
JPSHPWJJSVEEAX-UHFFFAOYSA-N
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
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
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Jun Nakamura et al.
Applied and environmental microbiology, 73(14), 4491-4498 (2007-05-22)
Corynebacterium glutamicum is a biotin auxotroph that secretes L-glutamic acid in response to biotin limitation; this process is employed in industrial L-glutamic acid production. Fatty acid ester surfactants and penicillin also induce L-glutamic acid secretion, even in the presence of
D W Konas et al.
The Journal of organic chemistry, 66(26), 8831-8842 (2001-12-26)
Electrophilic fluorination of enantiomerically pure 2-pyrrolidinones (4) derived from (L)-glutamic acid has been investigated as a method for the synthesis of single stereoisomers of 4-fluorinated glutamic acids. Reaction of the lactam enolate derived from 9 with NFSi results in a
Biochemical and biological properties of methotrexate analogs containing D-glutamic acid or D-erythro, threo-4-fluoroglutamic acid.
J J McGuire et al.
Biochemical pharmacology, 42(12), 2400-2403 (1991-11-27)
Clár Donnelly et al.
Applied microbiology and biotechnology, 77(3), 699-703 (2007-09-29)
Fluorinated amino acids are used as enzyme inhibitors, mechanistic probes and in the production of pharmacologically active peptides. Because enantiomerically pure 4-fluoroglutamate is difficult to prepare, the selective degradation of the L-isomer is a potentially convenient method of obtaining D-4-fluoroglutamate
J Dubois et al.
The Journal of biological chemistry, 258(13), 7897-7899 (1983-07-10)
Two pentapeptides Phe-Leu-X-Glu-Val where X is either the L-threo-gamma-fluoroglutamic acid or the L-erythro-isomer have been synthesized and tested as substrates in the vitamin K-dependent carboxylation. Both peptides are carboxylated, but the reaction occurs exclusively on the glutamic acid of the
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