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Merck

47306

Sigma-Aldrich

L-3-氟苯丙氨酸

≥99.0% (sum of enantiomers, HPLC)

别名:

3-氟-L-苯丙氨酸

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About This Item

经验公式(希尔记法):
C9H10FNO2
CAS号:
分子量:
183.18
Beilstein:
2725762
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.22

化驗

≥99.0% (sum of enantiomers, HPLC)

光學活性

[α]20/D −25±2°, c = 1% in H2O

反應適用性

reaction type: solution phase peptide synthesis

應用

peptide synthesis

SMILES 字串

N[C@@H](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)/t8-/m0/s1

InChI 密鑰

VWHRYODZTDMVSS-QMMMGPOBSA-N

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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P Giusti et al.
European journal of pharmacology, 116(3), 287-292 (1985-10-22)
It had previously been shown that D-phenylalanine and hydrocinnamic acid, two in vitro inhibitors of carboxypeptidase A, possess an analgesic action when injected i.p. in mice. We have studied the in vivo effects of indole-3-acetic acid, another carboxypeptidase A inhibitor
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
K Fukuda et al.
Current genetics, 20(6), 453-456 (1991-12-01)
o-Fluoro-DL-phenylalanine (OFP)-resistant mutants which overproduce beta-phenethyl-alcohol were isolated from a laboratory strain of Saccharomyces cerevisiae. Cells of one of the mutants accumulated tyrosine and phenylalanine 1.5-3 fold more than did wild-type cells. Its 3-deoxy-D-arabino-hepturosonate-7-phosphate (DAHP) synthase (EC 4.1.2.15), encoded by
W D Kingsbury et al.
Journal of medicinal chemistry, 26(12), 1725-1729 (1983-12-01)
A series of di- and tripeptides containing D- and L-m-fluorophenylalanine was prepared and tested in vitro for the ability to inhibit the growth of the yeast Candida albicans. The results demonstrate that peptides containing L-m-fluorophenylalanine inhibited the growth of C.
[Transport of phenylalanine in human brain by L-[2-18F]-fluorophenylalanine and PET].
S Miura et al.
Nihon rinsho. Japanese journal of clinical medicine, 49(7), 1537-1540 (1991-07-01)

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