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Article number:
7550650
CAS No.:
479-98-1
Formula:
C15H22O9
Chemical description:
Synonyms:
(2S,3R,4S,5S,6R)-2-[[(1S,4aR,5S,7aS)-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol; Aucuboside; Rhinanthin
Molecular weight:
346,33 g/mol
Aucubin prevents interleukin-1 beta induced inflammation and cartilage matrix degradation via inhibition of NF-?B signaling pathway in rat articular chondrocytes. Wang SN, Xie GP, Qin CH, Chen YR, Zhang KR, Li X, Wu Q, Dong WQ, Yang J, Yu B. Int Immunopharmacol. 2015 Feb;24(2):408-15. doi: 10.1016/j.intimp.2014.12.029. Epub 2015 Jan 6. *** Aucubin promotes neurite outgrowth in neural stem cells and axonal regeneration in sciatic nerves. Kim YM, Sim UC, Shin Y, Kim Kwon Y. Exp Neurobiol. 2014 Sep;23(3):238-45. doi: 10.5607/en.2014.23.3.238. Epub 2014 Sep 18. *** Aucubin, a naturally occurring iridoid glycoside inhibits TNF-a-induced inflammatory responses through suppression of NF-?B activation in 3T3-L1 adipocytes. Park KS.Cytokine. 2013 Jun;62(3):407-12. doi: 10.1016/j.cyto.2013.04.005. Epub 2013 Apr 20. *** Neuroprotective properties of aucubin in diabetic rats and diabetic encephalopathy rats. Xue HY, Lu YN, Fang XM, Xu YP, Gao GZ, Jin LJ. Mol Biol Rep. 2012 Oct;39(10):9311-8. doi: 10.1007/s11033-012-1730-9. Epub 2012 Jul 19.
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