3-Sulfanyl-D-valylglycyl-N-(L-tyrosyl)-L-phenylalanyl-D-valine, identified by its CAS number 105496-35-3, is a synthetic peptide that exhibits characteristics typical of peptide compounds. It is composed of a sequence of amino acids, which are the building blocks of proteins, and includes both D- and L-forms of amino acids, indicating its potential for specific biological activity. The presence of a sulfanyl group suggests that it may participate in redox reactions or serve as a nucleophile in biochemical processes. Peptides like this one often exhibit unique solubility properties, stability, and reactivity based on their amino acid composition and sequence. They can play roles in various biological functions, including signaling, enzyme activity, and as potential therapeutic agents. The specific arrangement of amino acids can influence its conformation, binding affinity, and overall biological activity, making it a subject of interest in medicinal chemistry and biochemistry. Further studies would be necessary to elucidate its precise biological functions and potential applications.

3-sulfanyl-D-valylglycyl-N-(L-tyrosyl)-L-phenylalanyl-D-valine

105496-35-3: 3-Sulfanyl-D-valylglycyl-N-(L-tyrosyl)-L-phenylalanyl-D-valine, identified by its CAS number 105496-35-3, is a synthetic peptide that exhibits characteristics typical of peptide compounds. It is composed of a sequence of amino acids, which are the building blocks of proteins, and includes both D- and L-forms of amino acids, indicating its potential for specific biological activity. The presence of a sulfanyl group suggests that it may participate in redox reactions or serve as a nucleophile in biochemical processes. Peptides like this one often exhibit unique solubility properties, stability, and reactivity based on their amino acid composition and sequence. They can play roles in various biological functions, including signaling, enzyme activity, and as potential therapeutic agents. The specific arrangement of amino acids can influence its conformation, binding affinity, and overall biological activity, making it a subject of interest in medicinal chemistry and biochemistry. Further studies would be necessary to elucidate its precise biological functions and potential applications.

<p>LY 190388 is a penicillamine-containing enkephalin analog used as an mu receptor agonist with analgesia activity.</p>

CAS 105496-35-3

3-sulfanyl-D-valylglycyl-N-(L-tyrosyl)-L-phenylalanyl-D-valine

LY 190388

Ref: TM-T27888