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Plantamajoside

Cat. No. M4720

All AbMole products are for research use only, cannot be used for human consumption.

Plantamajoside Structure
Size Price Availability Quantity
5mg USD 50 In stock
10mg USD 80 In stock
20mg USD 140 In stock
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Quality Control & Documentation
Biological Activity

Plantamajoside is a hydroxycinnamic acid, which used as a biomarker in chemotaxonomical studies. Plantamajoside has protective effects on LPS-induced acute lung injury (ALI) mice model. Plantamajoside has the potential for the treatment of pulmonary inflammation.

Customer Product Validations & Biological Datas
Source BMC Complement Altern Med (2017). Figure 2. Plantamajoside
Method Western blotting
Cell Lines HUVECs
Concentrations 10 μM
Incubation Time 24 h
Results In contrast, the co-treatment with 10 μM PM and 100 μg/mLof glycer-AGEs reduced protein expression
Source BMC Complement Altern Med (2017). Figure 1. Plantamajoside
Method MTT assay
Cell Lines HUVECs
Concentrations 10 μM
Incubation Time 24 h
Results We checked the PM cytotoxicity at 100 μM PM for 24 h and then treated with the PM only up to 10 μM PM after all experiments; NAC was not cytotoxic up to 1 mM for 24 h
Protocol (for reference only)
Cell Experiment
Cell lines MDA-MB-231 cells and 4T1 cells
Preparation method Cell viability assay was also performed on CHO cells to investigate the side effect of PMS on normal cells. The PMS concentration closed to IC50 (data not shown) for MDA-MB-231 cells and 4T1 cells at 36 h time point was chosen to treat CHO.
Concentrations 100 μg/mL
Incubation time 36 h
Animal Experiment
Animal models BALB/c mice
Formulation
Dosages 200 mg/kg
Administration oral
Chemical Information
Molecular Weight 640.59
Formula C29H36O16
CAS Number 104777-68-6
Solubility (25°C) DMSO: ≥ 30 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Pei S, et al. BMC Cancer. Plantamajoside, a potential anti-tumor herbal medicine inhibits breast cancer growth and pulmonary metastasis by decreasing the activity of matrix metalloproteinase-9 and -2.

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