Acetyl-α-MSH (11-13) hydrochloride salt

Modify Date: 2025-08-29 12:31:04

Acetyl-α-MSH (11-13) hydrochloride salt structure	Common Name	Acetyl-α-MSH (11-13) hydrochloride salt
	CAS Number	57899-96-4	Molecular Weight	383.49
	Density	1.2±0.1 g/cm3	Boiling Point	743.9±60.0 °C at 760 mmHg
	Molecular Formula	C₁₈H₃₃N₅O₄	Melting Point	N/A
	MSDS	N/A	Flash Point	403.7±32.9 °C

Use of Acetyl-α-MSH (11-13) hydrochloride salt

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
Synonym	More Synonyms

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.

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

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

Get all suppliers and price by the below link: