Flavonoides e Polifenóis

<p>Nordalbergin, a coumarin isolated from the bark of Dalbergia sissoo, can significantly induce the differentiation of HL-60 cells.</p>

<p>Applications Triclosan (3',5',6'-d3) O-β-D-Glucuronide Sodium Salt is an isotope labelled compound of Triclosan O-β-D-Glucuronide Sodium Salt (T774260), a metabolite of Triclosan (T774250).<br>References Moss, T. et al.: Food Chem. Toxicol., 38, 361 (2000); Wu, J. et al.: Sepu, 27, 724 (2009);<br></p>

<p>Stability Hygroscopic, Moisture Sensitive<br>Applications Triclosan O-Sulfate is a metabolite of the bacteriostat, Triclosan (T774250).<br>References Wu, J. et al.: Sepu, 27, 724 (2009);<br></p>

<p>Applications Secoisolariciresinol diglucoside (SDG) is a lignan found in flaxseed and is an emerging source in the functional food area. Flaxseed is the richest source of the lignan secoisolariciresinol diglucoside (SDG). SDG metabolites may protect against CVD and the metabolic syndrome by reducing lipid and glucose concentration, lowering blood pressure, and decreasing oxidative stress and inflammation.<br>References Lucas, E., et al.: J. Clin. Endocrinol Metab., 87, 1527 (2002), Choo, W., et al.: J. Food Compost. Anal., 20, 202 (2007), Sicilia, T., et al.: J. Agric. Food Chem., 51, 1181 (2003),<br></p>

<p>Applications Khellin is a compound present in the kella or picktooth fruit, used as a muscle relaxant.<br>References Shinde, P. et al.: Indian J. Nat. Prod. Res., 5, 40 (2014); Sztiller-Sikorska, M. et al.:<br></p>

<p>Applications Dihydroresveratrol is a natural phytoestrogen.<br></p>

<p>Applications 27-Deoxyactein has shown stimulation of osteoblast function and inhibits bone resorbing mediators in the treatment of osteoporosis. It is a derivative of Actein (A191800), a gamma secretase modulators derived from botanicals.<br>References Choi, E. et al. J. App. Toxicol., 33, 190 (2010); Findeis, M. et al.: ACS. Chem. Neurosci., 3, 941 (2012); Einbond, L. et al.: Fund. Clin. Pharm., 23, 311 (2009);<br></p>

<p>Applications Exhibits specific inhibitory activity against tyrosine kinases,including autophosphorylation of epidermal growth factor receptor kinase (IC50 - 2.6uM). Also inhibits other protein kinases through competitive inhibition of ATP. Inhibits tumor cell proliferation and induces tumor cell differentiation. Produces cell-cycle arrest and apoptosis in Jurat T-leukemia cells. However, it prevents anti-CD3 monoclonal antibody-induced thymic apoptosis. Genistein also inhibits topoisomerase II activity in vitro. Genistein has also been shown to inhibit the action of GABA on recombinant GABAA receptors2. uv(max)ethanol: 262.5 nm (e= 138). moderately sol. in hot alcohol<br>References Akiyama, T., et al.: J. Biol. Chem., 262, 5592 (1987), O'Dell, T.J., et al.: Nature, 353, 588 (1991), Aharonovits, O., et al.: Biochim Biophys. Acta, 1112, 181 (1992), Platanias, L.C., et al.: J. Biol. Chem., 267, 24053 (1992), Yoshida, H., et al.: Biochim. Biophys. Acta, 1137, 321 (1992), Uckun, F.M., et al.: Science, 267, 886 (1995)Merck Index 12th ed. 43952. Huang, R.Q.; Fang, M.J.; Dillon, G.H., Mol. Brain Res. 67: 177-183 (1999)<br></p>

<p>Applications A major Lidocaine metabolite.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Falany, C., et al.: Drug Metab. Disposition, 27, 1057 (1999), Gan, J., et al.: Chem. Res. Toxicol., 14, 672 (2001), Lienert, J., et al.: Envir. Sci. Technol., 41, 4471 (2007),<br></p>

<p>Stability Hygroscopic<br>Applications Urolithin D is used in biological studies to evaluate DNA gyrase inhibitory activity of ellagic acid derivatives.<br>References Weidner-Weels, M. A., et al: Bioorg. Med. Chem. Lett., 8, 97 (1998)<br></p>

<p>Stability Light Sensitive<br>Applications Urolithin B Glucuronide counteracts trimethylamine-N-oxide (TMAO)-induced cell damage and other detrimental effects of the cardiovascular systems triggered by TMAO.<br>References Savi, M., et al.: Molecules, 23, 549 (2018)<br></p>

<p>Applications Diosmetin 3’,7-Diglucuronide-d3 is labelled Diosmetin 3’,7-Diglucuronide (D485040), a metabolite of Diosmetin (D485000) which is a flavonoid often administered in the treatment of chronic venous insufficiency, hemorrhoids, and related affections.<br>References Silverstro, L., et al.: Anal. Bioanal. Chem., 405, 8295 (2013); Boutin, J., et al.; Drug Metab. Dispos., 21, 1157 (1993)<br></p>

<p>Applications Methyl trans-Cinnamate is one of the odour active compounds of Tahitian vanilla flavour and basil oil. Methyl trans-Cinnamate is naturally found in Magnolia liliflora oil, which is used to create a variety of nematicides. Methyl trans-Cinnamate also inhibits mushroom tyrosinase and has antimicrobial effects against Escherechia coli in food.<br>References Adams, A., et al.: J. Am. Oil Chem. Soc., 88, 201 (2011); Blank, A., et al.: Ind. Crop. Prod., 38, 93 (2012); Brunschwig, C., et al.: Food Res. Int., 46, 148 (2012); Huang, Q., et al.: J. Agr. Food Chem., 57, 2565 (2009)<br></p>

<p>Applications 2,4,5-Trichlorophenol-d2 is the labelled analogue of 2,4,5-Trichlorophenol (T774145), which is used as a broad range pesticide against insects, fungi, vegetation and bacteria. It has become a common environmental contaminant and probable human carcinogen.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Amer, S. et al.: Cytologia, 39, 633 (1974); Xu, X. wt l.: Occup. Environ. Med., 68, 557 (2011); Sinclair, C.J. et al.: Environ. Sci. Technol., 37, 4617 (2003);<br></p>

<p>Applications Silychristin is a new natural product has been isolated from silymarin, the hepatoprotective extract of milk thistle (Silybum marianum) fruits. Silychristin has been shown to be an antihepatotoxic flavonolignan.<br>References Smith, W.A., et al.: Planta. Med., 71, 877 (2005); Hong, L., et al.: Process. Biochem., 45, 799 (2010); Hitoshi, T., et al.: J. Chem. Soc., 11, 749 (1988);<br></p>

<p>Applications A metabolite of trans Resveratrol.<br>References Banerjee, S., et al.: Cancer Res., 62, 4945 (2002), Wang, L., et al.: J. Pharm. Sci., 93, 2448 (2004), Provinciali, M., et al.: Int. J. Cancer, 115, 36 (2005), Lancon, A., et al.: Drug Metab. Dispos., 35, 699 (2007),<br></p>