Identification | More | [Name]
O-PHOSPHO-L-TYROSINE | [CAS]
21820-51-9 | [Synonyms]
H-TYR(H2PO3)-OH H-TYR(PO3H2)-OH H-TYR(P)-OH L-3-[4-HYDROXYPHENYL]ALANINE 4'-PHOSPHATE L-TYROSINE O-PHOSPHATE O-PHOSPHO-L-TYROSINE O-PHOSPHORYL-L-TYROSINE PHOSPHOTYROSINE (S)-2-AMINO-3-(4-PHOSPHONOOXY-PHENYL)-PROPIONIC ACID H-Tyr(PO3)-OH H-L-Tyr(PO3H2)-OH L-Phosphotyrosine, (S)-2-Amino-3-(4-phosphonooxy-phenyl)-propionic acid (S)-2-Amino-3-(4-phosphonooxy-phenyl)-propionic ac L-3-(4-Hydroxyphenyl)alanine 4μ-phosphate, L-Tyrosine-O-phosphate L-Tyrosine-O-phosphoric acid O-Phosphono-L-tyrosine O-Phosphonotyrosine O-Phosphotyrosine Phosphoric acid 4-[(S)-2-carboxy-2-aminoethyl]phenyl ester | [Molecular Formula]
C9H12NO6P | [MDL Number]
MFCD00002603 | [Molecular Weight]
261.17 | [MOL File]
21820-51-9.mol |
Chemical Properties | Back Directory | [Appearance]
White Solid | [Melting point ]
226-227°C | [Boiling point ]
521.7±60.0 °C(Predicted) | [density ]
1.591±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C
| [pka]
1.24±0.30(Predicted) | [Usage]
Useful in the study of tyrosine-phosphorylation, which has been linked with the malignant transformation of cells by some RNA tumour viruses. | [BRN ]
3150815 | [CAS DataBase Reference]
21820-51-9(CAS DataBase Reference) |
Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
O-Phospho-L-tyrosine is used in the study of tyrosine-phosphorylation, which has been linked to the malignant transformation of cells by various RNA tumor viruses. Plays a role in signal transduction. | [Uses]
Useful in the study of tyrosine-phosphorylation, which has been linked with the malignant transformation of cells by some RNA tumour viruses. | [Uses]
Useful in the study of tyrosine-phosphorylation, which has been linked with the malignant transformation of cells by some RNA tumour viruses. | [Definition]
ChEBI: A non-proteinogenic L-alpha-amino acid that is L-tyrosine phosphorylated at the phenolic hydroxy group. | [Purification Methods]
Purify it by recrystallisation from H2O or H2O/EtOH. [Levene & Schormüller J Biol Chem 100 583 1933, Posternak & Graff Helv Chim Acta 28 1258 1945, Beilstein 14 III 1510.] |
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