GLU-THR-PRO-ASP-CYS-PHE-TRP-ORN-TYR-CYS-VAL
- Product Name
- GLU-THR-PRO-ASP-CYS-PHE-TRP-ORN-TYR-CYS-VAL
- CAS No.
- 479065-85-5
- Chemical Name
- GLU-THR-PRO-ASP-CYS-PHE-TRP-ORN-TYR-CYS-VAL
- Synonyms
- ORN8, UROTENSIN II, HUMAN;GLU-THR-PRO-ASP-CYS-PHE-TRP-ORN-TYR-CYS-VAL;L-Valine, L-α-glutamyl-L-threonyl-L-prolyl-L-α-aspartyl-L-cysteinyl-L-phenylalanyl-L-tryptophyl-L-ornithyl-L-tyrosyl-L-cysteinyl-, cyclic (5→10)-disulfide (9CI)
- CBNumber
- CB1224201
- Molecular Formula
- C63H83N13O18S2
- Formula Weight
- 1374.54
- MOL File
- Mol file
GLU-THR-PRO-ASP-CYS-PHE-TRP-ORN-TYR-CYS-VAL Property
- storage temp.
- Desiccate at -20°C
- solubility
- Soluble to 100 mM in DMSO and to 100 mM in ethanol
- form
- solid
- color
- White lyophilised
- Sequence
- Glu-Thr-Pro-Asp-Cys-Phe-Trp-{Orn}-Tyr-Cys-Val (Disulfide bridge:Cys5-Cys10)
GLU-THR-PRO-ASP-CYS-PHE-TRP-ORN-TYR-CYS-VAL Chemical Properties,Usage,Production
Description
Inhibitor of glycogen synthase kinase-3 (GSK-3); derived from FRAT1, the mammalian version of GSK-3-binding protein. Binds to GSK-3, inhibiting its interaction with axin, and also blocks GSK-3-catalyzed phosphorylation of axin and β-catenin. Does not affect GSK-3-mediated phosphorylation of glycogen synthase or eIF2B.
Uses
[Orn8]-Urotensin II (human), a peptide analog of urotensin II, is a UT receptor agonist. [Orn8]-Urotensin II (human) increases intracellular calcium levels in HEK293[1].
References
[1] Camarda V, et al. Urantide mimics urotensin-II induced calcium release in cells expressing recombinant UT receptors. Eur J Pharmacol. 2004 Sep 13;498(1-3):83-6. DOI:10.1016/j.ejphar.2004.07.089
[2] Camarda V, et al. A new ligand for the urotensin II receptor. Br J Pharmacol. 2002 Oct;137(3):311-4. DOI:10.1038/sj.bjp.0704895
GLU-THR-PRO-ASP-CYS-PHE-TRP-ORN-TYR-CYS-VAL Preparation Products And Raw materials
Raw materials
Preparation Products
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