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Moligand™, ≥96% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
CMX-2043 is a novel analogue of α-Lipoic Acid . 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
In Vitro
CMX-2043 (15-250 mM; 10 min) has great peroxyl radical absorbance capacity. CMX-2043 (1.5 μM) weakly inhibits spleen tyrosine kinase (Syk) and tunica interna endothelial cell kinase (Tie2). CMX-2043 (50 μM; 45 min) activates Akt phosporylation via PI3K pathway in A549 cells. CMX-2043 (2.5 mM; 30 min) diminishes the rise in cytosolic calcium in a concentration-dependent manner in CHO-M1-WT3 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only. ImmunofluorescenceCell Line: H9c2 (rat cardiac myocyte) cells Concentration: 50 μM Incubation Time: 3 hours Result: Showed brighter luorescence intensity in cells compared with control, indicating a stronger Akt phosphorylation effect.
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. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Ischemia-reperfusion injury (IRI) model in Sprague Dawley ratsDosage: 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.
Form:Solid
IC50& Target:EC50: 35 μM (IRK), tyrosine kinase, Akt
| Isómeros SMILES | C[C@@H](C(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)CCCC[C@@H]1CCSS1 |
|---|---|
| PubChem CID | 49802864 |
| Peso molecular | 406.52 |
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View spec sheet →| Solubilidad | DMSO : 20.83 mg/mL (51.24 mM; Need ultrasonic) |
|---|---|
| Sensibilidad | Moisture sensitive |
| Peso molecular | 406.500 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 12 |
| Exact Mass | 406.123 Da |
| Monoisotopic Mass | 406.123 Da |
| Topological Polar Surface Area | 183.000 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 517.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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