CMC2.24
Based on 1 Customer Validation
CMC2.24 (TRB-N0224), an orally active tricarbonylmethane agent, is effective against pancreatic tumor in mice by inhibiting Ras activation and its downstream effector ERK1/2 pathway. CMC2.24 is also a potent inhibitor of zinc-dependent MMPs with IC50s ranging from 2.0-69 μM. CMC2.24 alleviates osteoarthritis progression by restoring cartilage homeostasis and inhibiting chondrocyte apoptosis via the NF-κB/HIF-2α axis.
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- Pureté: 97.11%
- CAS No.: 1255639-43-0
- Formule: C26H21NO5
- Masse moléculaire:427.45
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Stockage:
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Activité biologique
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RAS |
MMP-1 69.8 μM (IC50) |
MMP-2 4.8 μM (IC50) |
MMP-3 2.9 μM (IC50) |
MMP-7 5 μM (IC50) |
MMP-8 4.5 μM (IC50) |
MMP-9 8 μM (IC50) |
MMP-12 2 μM (IC50) |
MMP-13 2.7 μM (IC50) |
MMP-14 15.3 μM (IC50) |
CMC2.24 (0-60 μM; 24 hours) inhibits pancreatic cancer growth in vitro[1].
CMC2.24 reduces STAT3Ser727 phosphorylation levels, induces mitochondrial reactive oxygen species and mitochondrial cell death in pancreatic cancer cells. CMC2.24 induces mitochondrial reactive oxygen species and intrinsic apoptosis[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:AsPC-1, Panc-1, MIA PaCa-2 and BxPC-3 PC cells
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Concentration:0-60 μM
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Incubation Time:24 hours
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Result:Inhibits PC cell growth in a concentration-dependent manner.
CMC2.24 inhibits the growth of human PC through a strong cytokinetic effect. CMC2.24 inhibits ERK signaling pathway in PC cells and xenografts[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Female immune deficient BALB/c nude mice[1]
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Dosage:50 mg/kg
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Administration:P.o.; five times per week during 17 days
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Result:Reduced the rate of growth over baseline by 66.9%.
Chemical Information
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CAS No. 1255639-43-0
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Appearance Solid
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Masse moléculaire 427.45
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Formule C26H21NO5
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Color Light yellow to orange
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SMILES
O=C(NC1=CC=CC=C1)C(C(/C=C/C2=CC=C(O)C=C2)=O)C(/C=C/C3=CC=C(O)C=C3)=O
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Synonyms
TRB-N0224
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
-20°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Solvant et solubilité
DMSO : < 1 mg/mL (insoluble or slightly soluble)
Pureté et documentation
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Fiche technique (273 KB)
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SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 KB)
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Instruction de manipulation (2659 KB)
Références
[1]. Mallangada NA, et al. A novel tricarbonylmethane agent (CMC2.24) reduces human pancreatic tumor growth in mice by targeting Ras. Mol Carcinog. 2018;57(9):1130-1143. [Content Brief]
[2]. Zhou Y, et al. Chemically modified curcumin (CMC2.24) alleviates osteoarthritis progression by restoring cartilage homeostasis and inhibiting chondrocyte apoptosis via the NF-κB/HIF-2α axis. J Mol Med (Berl). 2020;98(10):1479-1491. [Content Brief]
[3]. Zhang Y, et al. Design, synthesis and biological activity of new polyenolic inhibitors of matrix metalloproteinases: a focus on chemically-modified curcumins. Curr Med Chem. 2012;19(25):4348-4358. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)