Scutellarin

TargetMol
Product Code: TAR-T2789
Supplier: TargetMol
CodeSizePrice
TAR-T2789-10mg10mg£107.00
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TAR-T2789-1mL1 mL * 10 mM (in DMSO)£111.00
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TAR-T2789-25mg25mg£132.00
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TAR-T2789-50mg50mg£178.00
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TAR-T2789-100mg100mg£209.00
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Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Scutellarin, an active flavone isolated from Scutellaria baicalensis, can inhibit RANKL-mediated MAPK and NF-κB signaling pathway in osteoclasts, and down-regulate the STAT3/Girdin/Akt signaling in HCC cells.
CAS:
27740-01-8
Formula:
C21H18O12
Molecular Weight:
462.37
Pathway:
JAK/STAT signaling; Stem Cells; Proteases/Proteasome; PI3K/Akt/mTOR signaling; Microbiology/Virology; Cytoskeletal Signaling
Purity:
0.9932
SMILES:
c1cc(ccc1c1cc(=O)c2c(c(c(cc2o1)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)C(=O)O)O)O)O)O)O)O
Target:
Akt; HIV Protease; STAT

References

1. Ke Y, et al. Scutellarin suppresses migration and invasion of human hepatocellular carcinoma by inhibiting the STAT3/Girdin/Akt activity. Biochem Biophys Res Commun. 2016 Dec 18. pii: S0006-291X(16)32174-X. 2. Yang LL, et al. Differential regulation of baicalin and scutellarin on AMPK and Akt in promoting adipose cell glucose disposal. Biochim Biophys Acta. 2016 Nov 27;1863(2):598-606. 3. Wu CY, et al. Scutellarin attenuates microglia-mediated neuroinflammation and promotes astrogliosis in cerebral ischemia - a therapeutic consideration. Curr Med Chem. 2016 Nov 18. [Epub ahead of print] 4. Li Q, et al. Scutellarin attenuates vasospasm through the Erk5-KLF2-eNOS pathway after subarachnoid hemorrhage in rats. J Clin Neurosci. 2016 Dec;34:264-270. 5. Zhao, S., Sun, Y., Li, X., Wang, J., Yan, L., & Zhang, Z. et al. (2016). Scutellarin inhibits RANKL-mediated osteoclastogenesis and titanium particle-induced osteolysis via suppression of NF-?B and MAPK signaling pathway.?International Immunopharmacology,?40, 458-465. doi: 10.1016/j.intimp.2016.09.031 6. Chinnasamy S, Selvaraj G, Selvaraj C, et al. Combining in silico and in vitro approaches to identification of potent inhibitor against phospholipase A2 (PLA2)[J]. International Journal of Biological Macromolecules. 2020, 144: 53-66