| Weight | 223.228 g/mol |
|---|---|
| Formula | C11H13NO4 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
N-Acetyl-L-tyrosine (537-55-3)
N-acetyltyrosine · N-acetyltyrosine, (D)-isomer · acetyl-L-tyrosine
Score:
#1555 in Physics
,
#1632 in Biochemistry
,
#4656 in Chemistry
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- CHYMOTRYPSIN-CATALYZED HYDROLYSIS OF N-ACETYL- AND N-BENZOYL-L-TYROSINE P-NITROANILIDES. (Archives of Biochemistry and Biophysics, 1963)
- Amino acid solutions for premature neonates during the first week of life : the role of N-acetyl-L-cysteine and N-acetyl-L-tyrosine (Journal of Parenteral and Enteral Nutrition, 1994)
- Colorimetric detection and separation of chiral tyrosine based on N-acetyl-L-cysteine modified gold nanoparticles (Journal of Materials Chemistry, 2012)
- Kinetics of Iodination. I. A Comparison of the Kinetics of Iodination of N-Acetyl-L-Tyrosine and N-Acetyl-3-iodo-L-Tyrosine (Journal of the American Chemical Society, 1964)
- Delayed hypersensitivity to azobenzenearsonate-N-acetyl-L-tyrosine. In vivo and in vitro study. (European Journal of Immunology, 1971)
- N-acetyl-L-tyrosine and N-acetyl-L-cysteine as tyrosine and cysteine precursors during intravenous infusion in humans (Metabolism-clinical and Experimental, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N-acetyltyrosine
- N-acetyltyrosine, (D)-isomer
- acetyl-L-tyrosine
- N-acetyltyrosine, (DL)-isomer
-
SMILESCC(=O)NC(CC1=CC=C(C=C1)O)C(=O)O
-
InChIKeyCAHKINHBCWCHCF-UHFFFAOYSA-N
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Synthesis
Phenol
+
Reactant
(Friedel-Crafts alkylation)
acetamide
+
Reactant
(Alkylation of primary amines)
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N-Acetyl-L-tyrosine
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