57899-96-4

57899-96-4 structure

Name: Acetyl-α-MSH (11-13) hydrochloride salt
Chemical Name: (2S)-2-acetamido-6-amino-N-[(2S)-2-amino-3-methylbutanoyl]-N-propylhexanamide
CAS Number: 57899-96-4
Molecular Formula: C₁₈H₃₃N₅O₄
Molecular Weight: 383.49
Catalog: Research Areas Inflammation/Immunology
Create Date: 2017-06-07 22:46:55
Modify Date: 2024-01-09 13:56:31
Acetyl-α-MSH (11-13) is the acetylated C-terminal tripeptide of α-MSH with antipyretic and anti-inflammatory activities[1][2].

Name	(2S)-2-acetamido-6-amino-N-[(2S)-2-amino-3-methylbutanoyl]-N-propylhexanamide
Synonyms	Ac-Lys-pro-valnh2 N-Acetyl-L-lysyl-L-prolyl-L-valinamide L-Valinamide, N-acetyl-L-lysyl-L-prolyl- N-Acetyllysyl-prolyl-valinamide 1-Valinamide,N2-acetyl-L-lysyl-L-propyl

Description	Acetyl-α-MSH (11-13) is the acetylated C-terminal tripeptide of α-MSH with antipyretic and anti-inflammatory activities[1][2].
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Inflammation/Immunology
References	[1]. Schiöth HB, et al. New melanocortin 1 receptor binding motif based on the C-terminal sequence of alpha-melanocyte-stimulating hormone. Basic Clin Pharmacol Toxicol. 2006 Oct;99(4):287-93. [2]. Shimizu H, et al. Alpha-melanocyte-stimulating hormone (MSH) inhibits insulin secretion in HIT-T 15 cells. Peptides. 1995;16(4):605-8.Shimizu H, et al. Alpha-melanocyte-stimulating hormone (MSH) inhibits insulin secretion in HIT-T 15 cells. Peptides. 1995;16(4):605-8.