143617-02-1|Teupolioside|Teupolioside|-范德生物科技公司

Teupolioside

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names：
Teupolioside
CAS号：
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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询价

中文别名	(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
英文别名	Teupolioside; Lamiuside A; Teupolioside HTN; trans-Lamalboside;
CAS号	143617-02-1
SMILES	C[C@H]1[C@H](O)[C@@H](O)[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O2)[C@H](O[C@@H]3[C@@H](O)[C@H](OCCc4cc(O)c(O)cc4)O[C@H](CO)[C@H]3OC(/C=C/c5cc(O)c(O)cc5)=O)O1
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
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Teupolioside(CAS:143617-02-1):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Teupolioside is a putatively ameliorates colitis; isolated from Ajuga reptans.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

[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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