The chemical substance known as (Ac-Nle4,Gln5,D-Phe7,D-Trp9)-α-MSH (4-10) amide, with the CAS number 172617-89-9, is a synthetic peptide that is a derivative of the melanocyte-stimulating hormone (MSH). This peptide is characterized by its specific amino acid sequence, which includes modifications such as acetylation at the N-terminus and the incorporation of non-standard amino acids like D-phenylalanine and D-tryptophan. These modifications enhance its stability and biological activity. The peptide is known for its role in regulating pigmentation, appetite, and energy homeostasis, making it of interest in research related to obesity and metabolic disorders. Its structure allows it to interact with melanocortin receptors, which are involved in various physiological processes. The amide form indicates that the C-terminus is amidated, further contributing to its stability and receptor binding affinity. Overall, this compound is significant in pharmacological studies and potential therapeutic applications due to its biological functions and modified properties.

(Ac-Nle4,Gln5,D-Phe7,D-Trp9)-.alpha.-MSH (4-10) amide

172617-89-9: The chemical substance known as (Ac-Nle4,Gln5,D-Phe7,D-Trp9)-α-MSH (4-10) amide, with the CAS number 172617-89-9, is a synthetic peptide that is a derivative of the melanocyte-stimulating hormone (MSH). This peptide is characterized by its specific amino acid sequence, which includes modifications such as acetylation at the N-terminus and the incorporation of non-standard amino acids like D-phenylalanine and D-tryptophan. These modifications enhance its stability and biological activity. The peptide is known for its role in regulating pigmentation, appetite, and energy homeostasis, making it of interest in research related to obesity and metabolic disorders. Its structure allows it to interact with melanocortin receptors, which are involved in various physiological processes. The amide form indicates that the C-terminus is amidated, further contributing to its stability and receptor binding affinity. Overall, this compound is significant in pharmacological studies and potential therapeutic applications due to its biological functions and modified properties.

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CAS 172617-89-9

(Ac-Nle4,Gln5,D-Phe7,D-Trp9)-.alpha.-MSH (4-10) amide

N-Acetyl-L-norleucyl-L-glutaminyl-L-histidyl-D-phenylalanyl-L-arginyl-D-tryptophylglycinamide

Ref: 3D-FA109048