CAS 568588-77-2

L-Histidine,L-prolyl-L-valyl-L-asparaginyl-L-phenylalanyl-L-lysyl-L-phenylalanyl-L-leucyl-L-seryl-

Description:

The substance identified as "L-Histidine, L-prolyl-L-valyl-L-asparaginyl-L-phenylalanyl-L-lysyl-L-phenylalanyl-L-leucyl-L-seryl-" with CAS number 568588-77-2 is a peptide composed of multiple amino acids. This compound features a sequence of L-amino acids, which are the building blocks of proteins and play crucial roles in various biological processes. The presence of L-histidine suggests potential involvement in enzyme catalysis and buffering due to its imidazole side chain, while the other amino acids contribute to the peptide's overall structure and function. Peptides like this one can exhibit diverse biological activities, including hormone regulation, immune response modulation, and neurotransmission. The specific sequence and arrangement of amino acids determine the peptide's properties, such as solubility, stability, and interaction with biological targets. Additionally, the compound may be of interest in pharmaceutical research, particularly in drug design and development, due to its potential therapeutic applications. However, detailed studies would be necessary to elucidate its specific functions and characteristics in biological systems.

Formula: C₅₃H₇₇N₁₃O₁₂

Hemopressin(rat)

CAS: 568588-77-2

Peptide inhibitor for ep24.15, neurolysin & ACE with Ki 27.76, 3.43, 1.87 μM. Lowers blood pressure, modulates CB1 receptor, reduces pain & food intake.

Formula: C₅₃H₇₇N₁₃O₁₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 1088.27

Ref: TM-TP1901

Hemopressin (rat)

CAS: 568588-77-2

Hemopressin is a synthetic, orally active, insulin-sensitizing agent. Hemopressin modulates the activity of the insulin receptor by binding to the carboxy terminal domain. This leads to increased insulin sensitivity and glucose uptake in peripheral tissues. Hemopressin has been shown to be effective against experimental models of autoimmune diseases, such as diabetes mellitus type 1 and multiple sclerosis. The drug significantly decreased blood pressure in healthy rats and had no effect on cancer cells or bacterial surface.

Formula: C₅₃H₇₇N₁₃O₁₂

Purity: Min. 95%

Molecular weight: 1,088.3 g/mol

Ref: 3D-TXA58877