The chemical substance with the name "H-Ser-Gln-Asn-Phe-((r))-Pro-Ile-Val-Gln-OH" and CAS number "124869-92-7" is a peptide, specifically a sequence of amino acids that are linked by peptide bonds. This compound features a combination of hydrophilic and hydrophobic amino acids, which can influence its solubility and biological activity. The presence of serine (Ser), glutamine (Gln), asparagine (Asn), phenylalanine (Phe), proline (Pro), isoleucine (Ile), and valine (Val) suggests potential roles in protein structure and function, including enzyme activity, receptor binding, or signaling pathways. The "H-" at the beginning indicates that the peptide is in its free amino form, while the "OH" at the end signifies a carboxylic acid group, which is typical for peptides. The stereochemistry indicated by "((r))" suggests that the proline residue is in its "right-handed" or "D" configuration, which can affect the peptide's conformation and biological interactions. Overall, this peptide may have applications in research, therapeutics, or as a biochemical tool.

H-Ser-Gln-Asn-Phe-((r))-Pro-Ile-Val-Gln-OH

124869-92-7: The chemical substance with the name "H-Ser-Gln-Asn-Phe-((r))-Pro-Ile-Val-Gln-OH" and CAS number "124869-92-7" is a peptide, specifically a sequence of amino acids that are linked by peptide bonds. This compound features a combination of hydrophilic and hydrophobic amino acids, which can influence its solubility and biological activity. The presence of serine (Ser), glutamine (Gln), asparagine (Asn), phenylalanine (Phe), proline (Pro), isoleucine (Ile), and valine (Val) suggests potential roles in protein structure and function, including enzyme activity, receptor binding, or signaling pathways. The "H-" at the beginning indicates that the peptide is in its free amino form, while the "OH" at the end signifies a carboxylic acid group, which is typical for peptides. The stereochemistry indicated by "((r))" suggests that the proline residue is in its "right-handed" or "D" configuration, which can affect the peptide's conformation and biological interactions. Overall, this peptide may have applications in research, therapeutics, or as a biochemical tool.

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CAS 124869-92-7

H-Ser-Gln-Asn-Phe-((r))-Pro-Ile-Val-Gln-OH

H-Ser-Gln-Asn-Phe-psi(CH2NH)Pro-Ile-Val-Gln-OH

Ref: 3D-FS111055