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Scutellarin

Cat. No. M3970
Scutellarin Structure
Size Price Availability Quantity
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
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

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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