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ChemicalBook--->CAS DataBase List--->1255639-43-0

1255639-43-0

1255639-43-0 Structure

1255639-43-0 Structure
IdentificationBack Directory
[Name]

CMC2.24
[CAS]

1255639-43-0
[Synonyms]

CMC2.24
CMC2.24,CMC-2.24
4-Pentenamide, 5-(4-hydroxyphenyl)-2-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]-3-oxo-N-phenyl-, (4E)-
[Molecular Formula]

C26H21NO5
[MDL Number]

MFCD32899876
[MOL File]

1255639-43-0.mol
[Molecular Weight]

427.45
Chemical PropertiesBack Directory
[Boiling point ]

711.1±60.0 °C(Predicted)
[density ]

1.345±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C, protect from light
[solubility ]

DMSO : < 1 mg/mL (insoluble or slightly soluble)
[form ]

Solid
[pka]

8.28±0.59(Predicted)
[color ]

Light yellow to orange
Hazard InformationBack Directory
[Uses]

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[1][2][3].
[in vivo]

CMC2.24 (50 mg/kg; p.o.; five times per week during 17 days) inhibits the growth of pancreatic cancer xenografts[1].
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].

Animal Model:Female immune deficient BALB/c nude mice[1]
Dosage:50 mg/kg
Administration:P.o.; five times per week during 17 days
Result:Reduced the rate of growth over baseline by 66.9%.
[IC 50]

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)
[References]

[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. DOI:10.1002/mc.22830
[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. DOI:10.1007/s00109-020-01972-1
[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. DOI:10.2174/092986712802884295
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