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Teupolioside

NMR下載 COA and HPLC MSDS下載
names：
Teupolioside
CAS號(hào)：
143617-02-1
MDL Number：
MF(分子式)： C35H46O20 MW(分子量)： 786.73
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文別名	(2R,3R,4R,5R,6R)-4-(((2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-6-(3,4-dihydroxyphenethoxy)-5-hydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl (E)-3-(3,4-dihydroxyphenyl)acrylate
英文別名	Teupolioside; Lamiuside A; Teupolioside HTN; trans-Lamalboside;
CAS號(hào)	143617-02-1
Inchi	InChI=1S/C35H46O20/c1-14-24(43)27(46)32(55-34-28(47)26(45)25(44)21(12-36)51-34)35(50-14)54-31-29(48)33(49-9-8-16-3-6-18(39)20(41)11-16)52-22(13-37)30(31)53-23(42)7-4-15-2-5-17(38)19(40)10-15/h2-7,10-11,14,21-22,24-41,43-48H,8-9,12-13H2,1H3/b7-4+/t14-,21+,22+,24-,25-,26-,27+,28+,29+,30+,31+,32+,33+,34-,35-/m0/s1
InchiKey	SDRRSTAVRUERNC-GUTOYVNHSA-N
分子式 Formula	C35H46O20
分子量 Molecular Weight	786.73
溶解度Solubility
性狀	Solid powder
儲(chǔ)藏條件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

產(chǎn)品說(shuō)明	Teupolioside(CAS:143617-02-1):僅限應(yīng)用于工業(yè)或者科學(xué)研究過(guò)程中非醫(yī)療目的，不應(yīng)用于人類(lèi)或動(dòng)物的臨床診斷以及治過(guò)程療，該產(chǎn)品非藥用，非食用。
Introduction	Teupolioside is a putatively ameliorates colitis; isolated from Ajuga reptans.
Application1
Application2
Application3

警示圖
危險(xiǎn)性	Warning
危險(xiǎn)性警示
安全聲明
安全防護(hù)
備注

[1]Di Paola R, Esposito E, Mazzon E, Riccardi L, Caminiti R, Dal Toso R, Pressi G, Cuzzocrea S. Teupolioside, a phenylpropanoid glycosides of Ajuga reptans, biotechnologically produced by IRBN22 plant cell line, exerts beneficial effects on a rodent model of colitis. Biochem Pharmacol. 2009 Mar 1;77(5):845-57. doi: 10.1016/j.bcp.2008.11.010. Epub 2008 Nov 25. PubMed PMID: 19070602.

[2]Pastore S, Potapovich A, Kostyuk V, Mariani V, Lulli D, De Luca C, Korkina L. Plant polyphenols effectively protect HaCaT cells from ultraviolet C-triggered necrosis and suppress inflammatory chemokine expression. Ann N Y Acad Sci. 2009 Aug;1171:305-13. doi: 10.1111/j.1749-6632.2009.04684.x. PubMed PMID: 19723070.

[3] Prescott TA, Veitch NC, Simmonds MS. Direct inhibition of calcineurin by caffeoyl phenylethanoid glycosides from Teucrium chamaedrys and Nepeta cataria. J Ethnopharmacol. 2011 Oct 11;137(3):1306-10. doi: 10.1016/j.jep.2011.07.063. Epub 2011 Aug 6. PubMed PMID: 21843624.

[4] Korkina LG, Mikhal'chik E, Suprun MV, Pastore S, Dal Toso R. Molecular mechanisms underlying wound healing and anti-inflammatory properties of naturally occurring biotechnologically produced phenylpropanoid glycosides. Cell Mol Biol (Noisy-le-grand). 2007 May 30;53(5):84-91. PubMed PMID: 17543237.

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