ChemicalBook--->CAS DataBase List--->1039342-24-9

1039342-24-9

1039342-24-9 Structure

1039342-24-9 Structure
IdentificationBack Directory
[Name]

L-Alanine, L-tyrosyl-L-alanyl-L-arginyl-L-alanyl-L-alanyl-L-alanyl-L-arginyl-L-glutaminyl-L-alanyl-L-arginyl-L-alanyl-L-lysyl-L-alanyl-L-leucyl-L-alanyl-L-arginyl-L-glutaminyl-L-leucylglycyl-L-valyl-L-alanyl-
[CAS]

1039342-24-9
[Synonyms]

MMI-0100
L-Alanine, L-tyrosyl-L-alanyl-L-arginyl-L-alanyl-L-alanyl-L-alanyl-L-arginyl-L-glutaminyl-L-alanyl-L-arginyl-L-alanyl-L-lysyl-L-alanyl-L-leucyl-L-alanyl-L-arginyl-L-glutaminyl-L-leucylglycyl-L-valyl-L-alanyl-
[Molecular Formula]

C98H171N37O26
[MOL File]

1039342-24-9.mol
[Molecular Weight]

2283.64
Chemical PropertiesBack Directory
[density ]

1.46±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C, protect from light, stored under nitrogen
[form ]

Solid
[color ]

White to off-white
[Water Solubility ]

Water : 100 mg/mL (43.79 mM; Need ultrasonic)
Hazard InformationBack Directory
[Uses]

MMI-0100 is a cell-permeant peptide inhibitor of mitogen activated protein kinase activated protein kinase II (MK2). MMI-0100 reduces intimal hyperplasia ex vivo and in vivo. MMI-0100 suppresses IL-6 expression without effect on IL-8 expression. MMI-0100 suppresses fibrotic processes such as vein graft disease[1].
[in vivo]

MMI-0100 (100 μM; 28 days) inhibits intimal hyperplasia in a mouse vein graft model[1].

Animal Model:12-week-old C57Bl/6 wild type mice (intimal hyperplasia)[1]
Dosage:100 μM
Administration:vein graft, 28 days
Result:Diminished wall thickness at all postoperative time points in vein grafts treated with MMI-0100, with a ratio of 2.6-fold thicker at 4 weeks, compared to 4.7-fold thicker at 4 weeks in control grafts.
[storage]

Store at -20°C, protect from light, stored under nitrogen
[References]

[1] Akihito Muto, et al. Inhibition of Mitogen Activated Protein Kinase Activated Protein Kinase II with MMI-0100 reduces intimal hyperplasia ex vivo and in vivo. Vascul Pharmacol. Jan-Feb 2012;56(1-2):47-55. DOI:10.1016/j.vph.2011.07.008
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