The chemical substance with the name "H-Ala-Met-Gln-Met-Leu-Lys-Asp-Thr-Ile-Oh" and CAS number 334731-59-8 is a peptide composed of a sequence of amino acids. This peptide features a variety of functional groups characteristic of amino acids, including amine, carboxylic acid, and hydroxyl groups, which contribute to its solubility and reactivity. The presence of hydrophobic amino acids like Methionine and Leucine suggests that the peptide may have hydrophobic interactions, influencing its structure and biological activity. Additionally, the inclusion of charged residues such as Lysine and Aspartic acid indicates potential for ionic interactions, which can affect the peptide's stability and interaction with other biomolecules. The N-terminal acetylation (indicated by "H-" at the beginning) and the hydroxyl group at the C-terminus ("-Oh") may enhance its stability and solubility in biological systems. Overall, this peptide may exhibit specific biological activities, potentially serving roles in signaling or as a therapeutic agent, depending on its conformation and interactions within a biological context.

H-Ala-Met-Gln-Met-Leu-Lys-Asp-Thr-Ile-Oh

334731-59-8: The chemical substance with the name "H-Ala-Met-Gln-Met-Leu-Lys-Asp-Thr-Ile-Oh" and CAS number 334731-59-8 is a peptide composed of a sequence of amino acids. This peptide features a variety of functional groups characteristic of amino acids, including amine, carboxylic acid, and hydroxyl groups, which contribute to its solubility and reactivity. The presence of hydrophobic amino acids like Methionine and Leucine suggests that the peptide may have hydrophobic interactions, influencing its structure and biological activity. Additionally, the inclusion of charged residues such as Lysine and Aspartic acid indicates potential for ionic interactions, which can affect the peptide's stability and interaction with other biomolecules. The N-terminal acetylation (indicated by "H-" at the beginning) and the hydroxyl group at the C-terminus ("-Oh") may enhance its stability and solubility in biological systems. Overall, this peptide may exhibit specific biological activities, potentially serving roles in signaling or as a therapeutic agent, depending on its conformation and interactions within a biological context.

Custom research peptide; min purity 95%. For different specs please use the Peptide Quote Tool

HIV-1 gag Protein p24 (65-73) (isolates MAL/U455)

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CAS 334731-59-8

H-Ala-Met-Gln-Met-Leu-Lys-Asp-Thr-Ile-Oh

HIV-1 gag Protein p24 (65-73) (isolates MAL/U455)

Ref: 3D-PP50209

HIV-1 gag Protein p24 (65-73) (isolates MAL/U455) trifluoroacetate salt

Ref: 3D-FH109759