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27060-70-4

27060-70-4 Structure

27060-70-4 Structure
IdentificationBack Directory
[Name]

Pentagamavunon-1
[CAS]

27060-70-4
[Synonyms]

Pentagamavunon-1
[Molecular Formula]

C23H24O3
[MDL Number]

MFCD07958657
[MOL File]

27060-70-4.mol
[Molecular Weight]

348.43
Chemical PropertiesBack Directory
[Boiling point ]

562.1±50.0 °C(Predicted)
[density ]

1.232±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 50 mg/mL (143.50 mM)
[form ]

Solid
[pka]

10.12±0.40(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

Pentagamavunon-1 (PGV-1), a Curcumin analog with oral activity, targets on several molecular mechanisms to induce apoptosis including inhibition of angiogenic factors cyclooxygenase-2 (COX-2) and vascular endothelial growth factor (VEGF). PGV-1 inhibits NF-κB activation[1].
[in vivo]

Pentagamavunon-1 (PGV-1, po, 20 mg/kg) exhibits significant anti-tumor activity in PDX model, without obvious toxicity[1].

Animal Model:Human cancer cells in a xenograf mouse model[2].
Dosage:20mg/kg.
Administration:P.O. every 2 days for 20 days.
Result:Exhibited little decrease in body weight, nor a decrease in white and red blood cell counts in peripheral blood, nor any other efects in behavior and macroscopic appearance. Thus, PGV-1 was sufciently potent to suppress tumor formation in vivo, but exhibited little or no obvious adverse effects on the normal lineage of cells.
[References]

[1] Edy Meiyanto, et al. Curcumin Analog Pentagamavunon-1 (PGV-1) Sensitizes Widr Cells to 5-Fluorouracil Through Inhibition of NF-κB Activation. Asian Pac J Cancer Prev. 2018 Jan 27;19(1):49-56. DOI:10.22034/APJCP.2018.19.1.49
[2] Beni Lestari, et al. Pentagamavunon-1 (PGV-1) Inhibits ROS Metabolic Enzymes and Suppresses Tumor Cell Growth by Inducing M Phase (Prometaphase) Arrest and Cell Senescence. Sci Rep . 2019 Oct 16;9(1):14867. DOI:10.1038/s41598-019-51244-3
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