The chemical substance with the name "H-Glu-Glu-Lys-Leu-Ile-Val-Val-Ala-Phe-OH" and CAS number "188818-21-5" is a peptide composed of a sequence of amino acids, specifically glutamic acid (Glu), lysine (Lys), leucine (Leu), isoleucine (Ile), valine (Val), alanine (Ala), and phenylalanine (Phe). This peptide is characterized by its specific sequence, which influences its biological activity and properties. It is typically synthesized through solid-phase peptide synthesis and may exhibit various biological functions, including potential roles in signaling pathways or as a therapeutic agent. The presence of multiple hydrophobic amino acids suggests that it may have a tendency to adopt specific conformations in aqueous environments, which can affect its solubility and interaction with other biomolecules. Additionally, the C-terminal phenolic group (OH) indicates that it may have reactive properties, making it suitable for further chemical modifications or conjugations in research and pharmaceutical applications. Overall, this peptide's characteristics are defined by its amino acid composition and sequence, which dictate its structure and function.

H-Glu-Glu-Lys-Leu-Ile-Val-Val-Ala-Phe-OH

188818-21-5: The chemical substance with the name "H-Glu-Glu-Lys-Leu-Ile-Val-Val-Ala-Phe-OH" and CAS number "188818-21-5" is a peptide composed of a sequence of amino acids, specifically glutamic acid (Glu), lysine (Lys), leucine (Leu), isoleucine (Ile), valine (Val), alanine (Ala), and phenylalanine (Phe). This peptide is characterized by its specific sequence, which influences its biological activity and properties. It is typically synthesized through solid-phase peptide synthesis and may exhibit various biological functions, including potential roles in signaling pathways or as a therapeutic agent. The presence of multiple hydrophobic amino acids suggests that it may have a tendency to adopt specific conformations in aqueous environments, which can affect its solubility and interaction with other biomolecules. Additionally, the C-terminal phenolic group (OH) indicates that it may have reactive properties, making it suitable for further chemical modifications or conjugations in research and pharmaceutical applications. Overall, this peptide's characteristics are defined by its amino acid composition and sequence, which dictate its structure and function.

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CAS 188818-21-5

H-Glu-Glu-Lys-Leu-Ile-Val-Val-Ala-Phe-OH

H-Glu-Glu-Lys-Leu-Ile-Val-Val-Ala-Phe-OH trifluoroacetate salt

Ref: 3D-FG109063