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ChemicalBook--->CAS DataBase List--->566872-15-9

566872-15-9

566872-15-9 Structure

566872-15-9 Structure
IdentificationBack Directory
[Name]

STE-MPKKKPTPIQLNP-NH2
[CAS]

566872-15-9
[Synonyms]

STE-MEK1(13)
STE-MPKKKPTPIQLNP-NH2
STEARYL-MEK-1 DERIVED PEPTIDE INHIBITOR 1, AMIDE
ERK ACTIVATION INHIBITOR PEPTIDE I, CELL-PERMEABLE
STE-MET-PRO-LYS-LYS-LYS-PRO-THR-PRO-ILE-GLN-LEU-ASN-PRO-NH2
[Molecular Formula]

C86H153N19O17S
[MDL Number]

MFCD04974162
[MOL File]

566872-15-9.mol
[Molecular Weight]

1757.32
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[form ]

lyophilized solid
[color ]

white
[Water Solubility ]

water: 1mg/mL
DMSO: 5mg/mL
Hazard InformationBack Directory
[Uses]

STE-MEK1(13) (Ste-MPKKKPTPIQLNP-NH ) is a cell permeable ERK1/2 inhibitor (IC50: 13-30 μM). STE-MEK1(13) inhibits ERK1/2 phosphorylation[1][2].
[Biological Activity]

Cell permeable: yes''Primary Target
MEK''Product does not compete with ATP.''Reversible: yes
[References]

[1] Li G, et al. A novel cellular survival factor--the B2 subunit of vacuolar H+-ATPase inhibits apoptosis. Cell Death Differ. 2006 Dec;13(12):2109-17. DOI:10.1038/sj.cdd.4401970
[2] Whiteman M, et al. Peroxynitrite-modified collagen-II induces p38/ERK and NF-kappaB-dependent synthesis of prostaglandin E2 and nitric oxide in chondrogenically differentiated mesenchymal progenitor cells. Osteoarthritis Cartilage. 2006 May;14(5):460-70. DOI:10.1016/j.joca.2005.11.002
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