CAS 58690-81-6

Benzenepropanamide, α-(benzoylamino)-4-hydroxy-, (S)-

Description:

Benzenepropanamide, α-(benzoylamino)-4-hydroxy-, (S)-, with the CAS number 58690-81-6, is a chemical compound characterized by its amide functional group and a hydroxyl group attached to a benzene ring. This compound features a chiral center, which contributes to its stereochemistry, specifically the (S)- configuration. The presence of the benzoylamino group indicates that it has a benzoyl moiety linked to an amino group, which can influence its reactivity and interactions in biological systems. The hydroxyl group enhances its solubility in polar solvents and may also participate in hydrogen bonding, affecting its physical properties and biological activity. This compound may be of interest in pharmaceutical applications due to its potential biological activity, particularly in relation to its structural features that can interact with biological targets. As with many organic compounds, its stability, reactivity, and solubility can vary based on environmental conditions such as pH and temperature.

Formula: C₁₆H₁₆N₂O₃

InChI: InChI=1S/C16H16N2O3/c17-15(20)14(10-11-6-8-13(19)9-7-11)18-16(21)12-4-2-1-3-5-12/h1-9,14,19H,10H2,(H2,17,20)(H,18,21)/t14-/m0/s1

InChI key: InChIKey=QYBPBEKJXBRSGI-AWEZNQCLSA-N

SMILES: C([C@H](NC(=O)C1=CC=CC=C1)C(N)=O)C2=CC=C(O)C=C2

Synonyms:

• Benzenepropanamide, α-(benzoylamino)-4-hydroxy-, (S)-
• Bz-Tyr-NH2
• N-Benzoyl-4-hydroxy-<span class="text-smallcaps">L</span>-phenylalaninamide
• N-Benzoyl-<span class="text-smallcaps">L</span>-tyrosinamide
• N-Benzoyltyrosine amide
• Nalpha-(phenylcarbonyl)-L-tyrosinamide
• Nalpha-benzoyltyrosinamide
• N-Benzoyl-L-tyrosinamide
• N-Benzoyl-4-hydroxy-L-phenylalaninamide

Benzoyl-L-tyrosine amide

CAS: 58690-81-6

Benzoyl-L-tyrosine amide is a reaction intermediate that is a competitive inhibitor of serine proteases. It binds to the active site of the enzyme and inhibits the breakdown of proteins by blocking the access of other reactants. Benzoyl-L-tyrosine amide has been shown to inhibit proteolytic activity in subtilis, an enzyme isolated from Bacillus licheniformis. The amino acid composition and binding properties are similar to those found in natural substrates. Benzoyl-L-tyrosine amide has been synthesized and its binding affinity towards histidine residues has been determined by titration calorimetry and fluorophosphate assay.

Formula: C₁₆H₁₆N₂O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 284.31 g/mol

Ref: 3D-FB47592

N-Benzoyl-L-tyrosinamide

CAS: 58690-81-6

Formula: C₁₆H₁₆N₂O₃

Purity: 95.0%

Color and Shape: Solid, Crystalline

Molecular weight: 284.315

Ref: 10-F219794