CAS 19883-74-0
:3-Nitro-L-phénylalanine
- (2S)-2-Azaniumyl-3-(3-nitrophenyl)propanoate
- 3-Nitro-<span class="text-smallcaps">L</span>-phenylalanine
- 3-Nitrophenylalanine
- 3-nitro-L-phenylalanine
- <span class="text-smallcaps">L</span>-Phenylalanine, 3-nitro-
- Alanine, 3-(m-nitrophenyl)-, <span class="text-smallcaps">L</span>-
- L-3-Nitrophenylalanine
- NSC 21948
- Alanine, 3-(m-nitrophenyl)-, L-
- L-Phenylalanine, 3-nitro-
3-Nitro-L-phenylalanine, 95%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo SciFormule :C9H10N2O4Degré de pureté :95%Masse moléculaire :210.19L-Phenylalanine, 3-nitro-
CAS :Formule :C9H10N2O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :210.18673-Nitro-L-phenylalanine
CAS :3-Nitro-L-phenylalanineDegré de pureté :98%Masse moléculaire :210.19g/mol(S)-2-Amino-3-(3-nitrophenyl)propanoic acid
CAS :Formule :C9H10N2O4Degré de pureté :96%Couleur et forme :Off-white powderMasse moléculaire :210.189L-3-Nitrophenylalanine
CAS :Produit contrôléApplications L-3-Nitrophenylalanine is a derivative of L-Phenylalanine (P319415), and is used in the photocleavage of polypeptide backbones. L-Phenylalanine is an essential amino acid. L-Phenylalanine is biologically converted into L-tyrosine, another one of the DNA-encoded amino acids, which in turn is converted to L-DOPA and further converted into dopamine, norepinephrine, and epinephrine.
References Peters, F. et al.: Chem. Biol., 16, 148 (2009); Hollunger, G. et al.: Acta Pharmacol. Toxicol., 34, 391 (1974); Bagchi, S.P. et al.: Biochem. Pharmacol., 26, 900 (1977);Formule :C9H10N2O4Couleur et forme :NeatMasse moléculaire :210.193-Nitro-L-phenylalanine
CAS :3-Nitro-L-phenylalanine is a synthetic amino acid that has been shown to have antitumour activity. It inhibits the growth of cancer cells by interacting with the dehydrogenase enzyme in the reaction system and inhibiting the production of fatty acids and aldehydes. The nitro group on 3-Nitro-L-phenylalanine interacts with guanine, which prevents it from forming hydrogen bonds and stabilizing its structure. This destabilizes DNA structures and leads to cell death.
Formule :C9H10N2O4Degré de pureté :Min. 95%Masse moléculaire :210.19 g/molRef: 3D-FN50086
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