ChemicalBook--->CAS DataBase List--->436083-30-6

436083-30-6

436083-30-6 Structure

436083-30-6 Structure
IdentificationBack Directory
[Name]

JKC-363
[CAS]

436083-30-6
[Synonyms]

JKC-363
(DeaMino-Cys11,D-2-Nal14,Cys18)-b-MSH (11-22) aMide
(Deamino-Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) amide
(DEAMINO-CYS11,D-2-NAL14,CYS18)-BETA-MSH (11-22) AMIDE
MPR-GLU-HIS-D-NAL(2)-ARG-TRP-GLY-CYS-PRO-PRO-LYS-ASP-NH2
(Deamino-Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) amide, JKC-363
(Deamino-Cys11,D-2-Nal14,Cys18)-β-MSH (11-22) amide, JKC-363
(DEAMINO-CYS11,D-ALA(2-NAPHTHYL)14,CYS18)-BETA-MSH (11-22) AMIDE
3-MERCAPTOPROPIONYL-GLU-HIS-D-2-NAL-ARG-TRP-GLY-CYS-PRO-PRO-LYS-ASP-NH2
(Deamino-Cys11,D-2-Nal 14,Cys18)-b-MSH (11-22) amide trifluoroacetate salt
Mpr-Glu-His-D-Nal(2)-Arg-Trp-Gly-Cys-Pro-Pro-Lys-Asp-NH2 (Disulfide bridge Mpr1-Cys8)
[DEAMINO-CYS11, B-(2-NAPHTHYL)-D-ALA14, CYS18]-BETA-MELANOCYTE STIMULATING HORMONE AMIDE FRAGMENT 11-22
[Deamino-Cys11, β-(2-Naphthyl)-D-Ala14, Cys18]-β-Melanocyte Stimulating Hormone Amide Fragment 11-22
L-α-Asparagine, N-(3-mercapto-1-oxopropyl)-L-α-glutamyl-L-histidyl-3-(2-naphthalenyl)-D-alanyl-L-arginyl-L-tryptophylglycyl-L-cysteinyl-L-prolyl-L-prolyl-L-lysyl-, cyclic (1→7)-disulfide
[Molecular Formula]

C69H91N19O16S2
[MDL Number]

MFCD06636638
[MOL File]

436083-30-6.mol
[Molecular Weight]

1506.71
Chemical PropertiesBack Directory
[density ]

1.56±0.1 g/cm3(Predicted)
[storage temp. ]

-15°C
[form ]

Powder
[pka]

4.07±0.10(Predicted)
[color ]

White to off-white
[Water Solubility ]

Soluble to 1 mg/ml in water
[Sequence]

{Mpa}-Glu-His-{D-2-Nal}-Arg-Trp-Gly-Cys-Pro-Pro-Lys-Asp-NH2 (Disulfide bridge:Mpa1-Cys8)
Safety DataBack Directory
[Safety Statements ]

22-24/25
Hazard InformationBack Directory
[Uses]

JKC363, a selective melanocortin MC4 receptor antagonist, has a 90-fold higher affinity at the MC4 receptor (IC50=0.5 nM) than at the MC3 receptor (44.9 nM). JKC-363 blocks the stimulatory effect of α-MSH on TRH release. Anti-hyperalgesic effect[1][2].
[IC 50]

MC4R
[References]

[1] Kim MS, et al. Effects of melanocortin receptor ligands on thyrotropin-releasing hormone release: evidence for the differential roles of melanocortin 3 and 4 receptors. J Neuroendocrinol. 2002;14(4):276-282. DOI:10.1046/j.1365-2826.2002.00769.x
[2] Bellasio S, et al. Melanocortin receptor agonists and antagonists modulate nociceptive sensitivity in the mouse formalin test. Eur J Pharmacol. 2003;482(1-3):127-132. DOI:10.1016/j.ejphar.2003.09.017
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