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Scutellarin

Cat. No. M3970

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

Scutellarin Structure
Size Price Availability Quantity
5mg USD 35  USD35 In stock
10mg USD 50  USD50 In stock
25mg USD 90  USD90 In stock
50mg USD 150  USD150 In stock
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Quality Control & Documentation
Biological Activity

Scutellarin, an active flavone isolated from Scutellaria baicalensis, can down-regulates the STAT3/Girdin/Akt signaling in HCC cells, and inhibits RANKL-mediated MAPK and NF-κB signaling pathway in osteoclasts. Scutellarin is active against HIV-1IIIB, HIV-1(74V) and HIV-1KM018 with EC50s of 26 μM, 253 μM and 136 μM, respectively. Scutellarin inhibited lipopolysaccharide (LPS)-induced production of proinflammatory mediators such as nitric oxide (NO), tumor necrosis factor α (TNFα), interleukin-1β (IL-1β) and reactive oxygen species (ROS), suppressed LPS-stimulated inducible nitric oxide synthase (iNOS), TNFα, and IL-1β mRNA expression in rat primary microglia or BV-2 mouse microglial cell line. Scutellarin inhibited LPS-induced nuclear translocation and DNA binding activity of nuclear factor κB (NF-κB). Scutellarin dose-dependently inhibited intracellular LPS-induced release of caspase-11p26 (indicative of caspase-11 activation) and generation of N-terminal fragment of gasdermin D (GSDMD-NT), leading to reduced pyroptosis in macrophages. Scutellarin also suppressed LPS-induced caspase-11 activation and pyroptosis in RAW 264.7 cells lacking ASC expression.

Product Citations
Customer Product Validations & Biological Datas
Source Int J Clin Exp Pathol 2020 Feb. Figure 1. Scutellarin (Abmole Bioscience, USA)
Method tail vein
Cell Lines BALB/C nude mice
Concentrations 60 mg/kg
Incubation Time -
Results Staining of the tumor sections with H&E revealed loss of cellular architecture with hypercellularity in the controls, while BTB+STN treatment depicted significant pyknosis, compared to BTB or STN treated mice.
Chemical Information
Molecular Weight 462.36
Formula C21H18O12
CAS Number 27740-01-8
Solubility (25°C) DMSO 90 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Jiezhou Ye, et al. Acta Pharm Sin B. Scutellarin inhibits caspase-11 activation and pyroptosis in macrophages via regulating PKA signaling

[2] Tang H, et al. Pharmacol Biochem Behav. Neuroprotective effects of scutellarin and scutellarein on repeatedly cerebral ischemia-reperfusion in rats.

[3] Wang S, et al. Neuroscience. Neuroprotection of Scutellarin is mediated by inhibition of microglial inflammatory activation.

[4] Lin LL, et al. J Cardiovasc Pharmacol. Protective effects of scutellarin and breviscapine on brain and heart ischemia in rats.

[5] Huang JM, et al. Eur J Drug Metab Pharmacokinet. Pharmacokinetics of scutellarin and its aglycone conjugated metabolites in rats.

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Keywords: Scutellarin supplier, STAT, inhibitors, activators

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