CAS 1948-71-6

N-Acetyl-L-tyrosinamide

Description:

N-Acetyl-L-tyrosinamide is an organic compound derived from the amino acid L-tyrosine, characterized by the presence of an acetyl group attached to the amino group of the tyrosine molecule. This modification enhances its solubility and stability compared to its parent compound. The substance is typically a white to off-white crystalline powder, and it is soluble in polar solvents such as water and ethanol. N-Acetyl-L-tyrosinamide is of interest in biochemical research due to its potential role in various metabolic pathways and its applications in the synthesis of pharmaceuticals. It may exhibit antioxidant properties, contributing to its relevance in studies related to neuroprotection and other health benefits. The compound's molecular structure includes a phenolic hydroxyl group, which is characteristic of tyrosine derivatives, and it may participate in various chemical reactions typical of amides and acetylated compounds. As with many biochemical substances, handling should be done with care, following appropriate safety protocols.

Formula: C₁₁H₁₄N₂O₃

InChI: InChI=1S/C11H14N2O3/c1-7(14)13-10(11(12)16)6-8-2-4-9(15)5-3-8/h2-5,10,15H,6H2,1H3,(H2,12,16)(H,13,14)/t10-/m0/s1

InChI key: InChIKey=RJNKBEQRBIJDNM-JTQLQIEISA-N

SMILES: C([C@H](NC(C)=O)C(N)=O)C1=CC=C(O)C=C1

Synonyms:

• (2S)-2-Acetamido-3-(4-hydroxyphenyl)propanamide
• (S)alpha-(Acetylamino)-4-hydroxybenzenepropanamide
• (αS)-α-(Acetylamino)-4-hydroxybenzenepropanamide
• Ac-Tyr-Nh2
• Benzenepropanamide, alpha-(acetylamino)-4-hydroxy-, (S)-
• Benzenepropanamide, α-(acetylamino)-4-hydroxy-, (S)-
• Benzenepropanamide, α-(acetylamino)-4-hydroxy-, (αS)-
• Hydrocinnamamide, α-acetamido-p-hydroxy-, <span class="text-smallcaps">L</span>-
• N-Acetyl-4-hydroxy-<span class="text-smallcaps">L</span>-phenylalaninamide
• N-Acetyl-<span class="text-smallcaps">L</span>-tyrosinamide
• N-Acetyl-<span class="text-smallcaps">L</span>-tyrosine amide
• N-Acetyltyrosylamide
• N-acetyltyrosinamide
• Nalpha-acetyl-L-tyrosinamide
• Hydrocinnamamide, α-acetamido-p-hydroxy-, L-

Ac-Tyr-NH₂

CAS: 1948-71-6

N-Acetyl-L-tyrosinamide showed potential as an active ingredient in anti-wrinkle creams.

Formula: C₁₁H₁₄N₂O₃

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 222.24

Ref: 01-4001968

N-Acetyl-L-tyrosinamide

CAS: 1948-71-6

Formula: C₁₁H₁₄N₂O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 222.2405

Ref: IN-DA003SP4

(S)-2-Acetamido-3-(4-hydroxyphenyl)propanamide

CAS: 1948-71-6

(S)-2-Acetamido-3-(4-hydroxyphenyl)propanamide

Purity: 98%

Molecular weight: 222.24g/mol

Ref: 54-OR95227

AC-TYR-NH2

CAS: 1948-71-6

Formula: C₁₁H₁₄N₂O₃

Purity: 95%

Molecular weight: 222.244

Ref: 10-F470194

Acetyl-L-tyrosine amide

CAS: 1948-71-6

Acetyl-L-tyrosine amide is an analog of L-tyrosine that is used as an active substance in the field of uv absorption. Acetyl-L-tyrosine amide reacts with sodium hydroxide to form a soluble salt, which has been shown to have binding constants that are comparable to those of human serum. This compound also has fluorescence properties and can be used for the determination of neutral pH. The reaction products formed between acetyl-L-tyrosine amide and sodium hydroxide are hydrolyzed by acids and yield a molecule with rotameric properties. These rotameric properties can be modeled using a protein model without affecting the stability or function of the protein.

Formula: C₁₁H₁₄N₂O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 222.24 g/mol

Ref: 3D-FA47448

N-Acetyl-L-tyrosine Amide

Controlled Product

CAS: 1948-71-6

Applications N-Acetyl-L-tyrosine Amide is an analogue of L-tyrosine which stimulate the transport of L-Tyr, mainly by the ASC system.
References Jara, J.R., et al.: Melanoma Res., 1(1), 15 (1991),

Formula: C₁₁H₁₄N₂O₃

Color and Shape: Neat

Molecular weight: 222.24

Ref: TR-A189740

Ac-Tyr-NH2

CAS: 1948-71-6

Ac-Tyr-NH2 is a rotameric peptide that has been shown to inhibit the growth of bacteria. It is a neutral compound and does not have any detectable effect on human serum. Ac-Tyr-NH2 has been shown to react with tryptophan, which may be due to its acid hydrolysis. This peptide also has an active role in the production of reaction products and the formation of model proteins. Ac-Tyr-NH2 has been shown to have an optical property of fluorescence, which can be used for skin reactions or uv absorption.

Formula: C₁₁H₁₄N₂O₃

Purity: Min. 95%

Molecular weight: 222.24 g/mol

Ref: 3D-SYA-3009