N-T-boc-tyr-D-ala-gly, with the CAS number 64410-47-5, is a synthetic peptide derivative that features a combination of amino acids, specifically tyrosine (Tyr), D-alanine (D-Ala), and glycine (Gly). The "N-T-boc" designation indicates that the amino group of the tyrosine residue is protected by a tert-butyloxycarbonyl (Boc) group, which is commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. This compound is typically utilized in research and pharmaceutical applications, particularly in the development of peptide-based drugs and as a building block in peptide synthesis. Its structure allows for specific interactions in biological systems, making it valuable in studies related to protein function and drug design. The presence of the D-amino acid (D-Ala) can influence the peptide's stability and bioactivity, as D-amino acids are often less susceptible to enzymatic degradation compared to their L-counterparts. Overall, N-T-boc-tyr-D-ala-gly serves as an important tool in the field of medicinal chemistry and peptide research.

N-T-boc-tyr-D-ala-gly

64410-47-5: N-T-boc-tyr-D-ala-gly, with the CAS number 64410-47-5, is a synthetic peptide derivative that features a combination of amino acids, specifically tyrosine (Tyr), D-alanine (D-Ala), and glycine (Gly). The "N-T-boc" designation indicates that the amino group of the tyrosine residue is protected by a tert-butyloxycarbonyl (Boc) group, which is commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. This compound is typically utilized in research and pharmaceutical applications, particularly in the development of peptide-based drugs and as a building block in peptide synthesis. Its structure allows for specific interactions in biological systems, making it valuable in studies related to protein function and drug design. The presence of the D-amino acid (D-Ala) can influence the peptide's stability and bioactivity, as D-amino acids are often less susceptible to enzymatic degradation compared to their L-counterparts. Overall, N-T-boc-tyr-D-ala-gly serves as an important tool in the field of medicinal chemistry and peptide research.

Boc-Tyr-D-ala-Gly-OH

(6S,9R)-6-(4-Hydroxybenzyl)-2,2,9-trimethyl-4,7,10-trioxo-3-oxa-5,8,11-triazatridecan-13-oic acid

CAS 64410-47-5

N-T-boc-tyr-D-ala-gly

Boc-Tyr-D-ala-Gly-OH

Ref: IN-DA00EB7L

(6S,9R)-6-(4-Hydroxybenzyl)-2,2,9-trimethyl-4,7,10-trioxo-3-oxa-5,8,11-triazatridecan-13-oic acid

Ref: 54-OR1059941