| Weight | 165.192 g/mol |
|---|---|
| Formula | C9H11NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
D-phenylalanine (673-06-3)
Score:
#159 in Biochemistry
,
#681 in Biology
,
#733 in Chemistry
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- 4-Norleucine, 7-D-phenylalanine-alpha-melanocyte-stimulating hormone: a highly potent alpha-melanotropin with ultralong biological activity (Proceedings of the National Academy of Sciences of the United States of America, 1980)
- Synthesis of gold nanoplates by aspartate reduction of gold chlorideElectronic supplementary information (ESI) available: Fig. S1. UV/Visible-NIR extinction spectra of an aqueous dispersion of gold nanoparticles synthesized by tyrosine (a), phenylalanine (b), lysine (c), aspartate (d) and tryptophan (e). See http://www.rsc.org/suppdata/cc/b3/b315732f/ (Chemical Communications, 2004)
- Preparation of fluoro- and hydroxy-4-(phosphonomethyl)-D,L-phenylalanine suitably protected for solid-phase synthesis of peptides containing hydrolytically stable analogs of O-phosphotyrosine (Journal of Organic Chemistry, 1993)
- The coimmobilization of d-amino acid oxidase and catalase enables the quantitative transformation of d-amino acids (d-phenylalanine) into -keto acids (phenylpyruvic acid) (Enzyme and Microbial Technology, 1998)
- tude electrochimique de l'oxydation de la dihydroxy-3,4 phnylalanine (Dopa): Mcanisme d'oxydation des catchols en milieu acide (Journal of Electroanalytical Chemistry, 1974)
- Ethanol inhibition of N-methyl-D-aspartate receptors is reduced by site-directed mutagenesis of a transmembrane domain phenylalanine residue. (Journal of Biological Chemistry, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)CC(C(=O)O)N
-
InChIKeyCOLNVLDHVKWLRT-UHFFFAOYSA-N
- Pubchem - D-phenylalanine
- Wikipedia - D-phenylalanine
Phenylalanine (Phe or F) is an -amino acid with the formula C 9H 11NO 2. It can be viewed as a benzyl group substituted for the methyl group of alanine, or a phenyl group in place of a terminal hydrogen of alanine. This essential amino acid is classified as neutral, and nonpolar because of the inert and hydrophobic nature of the benzyl side chain.
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