ChemicalBook--->CAS DataBase List--->910627-26-8

910627-26-8

910627-26-8 Structure

910627-26-8 Structure
IdentificationBack Directory
[Name]

CMX-2043
[CAS]

910627-26-8
[Synonyms]

LIPEA
LIP-EA
CMX-2043
R-LIP-EA-OH
CMX2043,CMX 2043
L-Alanine, N-[5-(3R)-1,2-dithiolan-3-yl-1-oxopentyl]-L-α-glutamyl-
[Molecular Formula]

C16H26N2O6S2
[MOL File]

910627-26-8.mol
[Molecular Weight]

406.517
Chemical PropertiesBack Directory
[Boiling point ]

775.7±60.0 °C(Predicted)
[density ]

1.316±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

3.39±0.10(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

CMX-2043 is a novel analogue of α-Lipoic Acid.html" class="link-product" target="_blank">α-Lipoic Acid (HY-N0492). CMX-2043 is effective in antioxidant effect, activation of insulin receptor kinase, soluble tyrosine kinase, and Akt phosphorylation. CMX-2043 shows protection against ischemia-reperfusion injury (IRI) in rat model[1][2].
[in vivo]

CMX-2043 (50-200 mg/kg, 5 mL; p.o.; single dose) reduces myocardial ischemia-reperfusion injury (IRI) as measured by the myocardial infarct to area at risk (MI-AR) ratio and the incidence of arrhythmia[2].

Animal Model:Ischemia-reperfusion injury (IRI) model in Sprague Dawley rats[2]
Dosage:50, 100, and 200 mg/kg; 5 mL of normal saline solution containing 2% vanilla extract as flavoring
Administration:Oral gavage; single dose; induced IRI 30-60 min after treatment
Result:Induced arrhythmia and mortality of rats with reducing the ratio of myocardial infarct to area at risk.
[References]

[1] Alan S Lader, et al. CMX-2043 Mechanisms of Action In Vitro. J Cardiovasc Pharmacol. 2016 Sept;68:241-247.
[2] Baguisi A, et al. CMX-2043 Efficacy in a Rat Model of Cardiac Ischemia-Reperfusion Injury. J Cardiovasc Pharmacol Ther. 2016 Nov;21(6):563-569. DOI:10.1177/1074248416640118
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