CAS 24787-87-9

L-Alanine, N-[(phenylmethoxy)carbonyl]-L-seryl-

Description:

L-Alanine, N-[(phenylmethoxy)carbonyl]-L-seryl- is a synthetic amino acid derivative characterized by its structure, which includes an alanine residue and a serine residue linked through a peptide bond. The compound features a phenylmethoxycarbonyl (Pmc) protecting group, which is commonly used in peptide synthesis to protect the amino group of the serine residue. This modification enhances the stability and solubility of the compound, making it useful in various biochemical applications, including peptide synthesis and drug development. The presence of both L-alanine and L-serine, which are naturally occurring amino acids, suggests that this compound may exhibit biological activity, potentially influencing protein structure and function. Additionally, the compound's molecular interactions can be influenced by the aromatic phenyl group, which may contribute to its hydrophobic characteristics. Overall, L-Alanine, N-[(phenylmethoxy)carbonyl]-L-seryl- is a versatile compound with applications in research and pharmaceutical development, particularly in the context of peptide chemistry.

Formula: C₁₄H₁₈N₂O₆

InChI: InChI=1S/C14H18N2O6/c1-9(13(19)20)15-12(18)11(7-17)16-14(21)22-8-10-5-3-2-4-6-10/h2-6,9,11,17H,7-8H2,1H3,(H,15,18)(H,16,21)(H,19,20)/t9-,11-/m0/s1

InChI key: InChIKey=VWPKWOHWTBYMEQ-ONGXEEELSA-N

SMILES: [C@H](C(N[C@H](C(O)=O)C)=O)(NC(OCC1=CC=CC=C1)=O)CO

Synonyms:

• <span class="text-smallcaps">L</smallcap>-Alanine, N-[(phenylmethoxy)carbonyl]-<smallcap>L</span>-seryl-
• <span class="text-smallcaps">L</smallcap>-Alanine, N-[N-[(phenylmethoxy)carbonyl]-<smallcap>L</span>-seryl]-
• Alanine, N-(N-carboxy-<span class="text-smallcaps">L</smallcap>-seryl)-, N-benzyl ester, <smallcap>L</span>-
• N-[(benzyloxy)carbonyl]serylalanine
• NSC 333744
• Alanine, N-(N-carboxy-L-seryl)-, N-benzyl ester, L-
• L-Alanine, N-[(phenylmethoxy)carbonyl]-L-seryl-
• L-Alanine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-

Z-Ser-Ala-OH

CAS: 24787-87-9

Formula: C₁₄H₁₈N₂O₆

Purity: 97%

Color and Shape: Solid

Molecular weight: 310.3025

Ref: IN-DA00C1HZ

Z-Ser-Ala-OH

CAS: 24787-87-9

Z-Ser-Ala-OH is an n-terminal and c-terminal carbohydrate that has been synthesized by chemoenzymatic methods. It is a racemic mixture of the two enantiomers, Z-serine and L-serine. Z-Ser-Ala-OH is a chiral compound with a specific rotation (alpha) of -35.6° (c=1 in methanol). This product can be used as an acylase substrate for the enzymatic cleavage of beta-(1→4)-linked alpha-(1→2)-linked glycosidic bonds to produce oligosaccharides with alpha-(1→3)-linked alpha-(1→6)-linked glycosidic bonds. The hydrolysis of the ester group can also be carried out under acidic conditions to produce phenylacetates and phenylacetyls.

Formula: C₁₄H₁₈N₂O₆

Purity: Min. 95%

Molecular weight: 310.3 g/mol

Ref: 3D-FS111514