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ChemicalBook--->CAS DataBase List--->57899-96-4

57899-96-4

57899-96-4 Structure

57899-96-4 Structure
IdentificationBack Directory
[Name]

AC-LYS-PRO-VAL-NH2
[CAS]

57899-96-4
[Synonyms]

α-MSH(11-13)
AC-LYS-PRO-VAL-NH2
Acetyl-a-MSH-(11-13
AC-ALPHA-MSH (11-13)
Acetyl-α-MSH (11-13)
N-AC-LYS-PRO-VAL-NH2
ACETYL-ALPHA-MSH (11-13)
N-acetyllysyl-prolyl-valinamide
Acetyl-α-MSH (11-13) hydrochloride salt
L-Valinamide, N2-acetyl-L-lysyl-L-prolyl-
Acetyl-alpha-MSH (11-13) hydrochloride salt
(2S)-2-acetamido-6-amino-N-[(2S)-2-amino-3-methylbutanoyl]-N-propylhexanamide
(S)-1-((S)-2-Acetamido-6-aminohexanoyl)-N-((S)-1-amino-3-methyl-1-oxobutan-2-yl)pyrrolidine-2-carboxamide
[Molecular Formula]

C18H33N5O4
[MDL Number]

MFCD00237182
[MOL File]

57899-96-4.mol
[Molecular Weight]

383.49
Chemical PropertiesBack Directory
[Boiling point ]

743.9±60.0 °C(Predicted)
[density ]

1.170±0.06 g/cm3(Predicted)
[storage temp. ]

-15°C
[pka]

13.44±0.20(Predicted)
Hazard InformationBack Directory
[Uses]

Acetyl-α-MSH (11-13) is the acetylated C-terminal tripeptide of α-MSH with antipyretic and anti-inflammatory activities[1][2].
[References]

[1] Schi?th 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. DOI:10.1111/j.1742-7843.2006.pto_459.x
[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. DOI:10.1016/0196-9781(94)00197-e
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