Flavonoids and Polyphenols

<p>Stability Light Sensitive<br>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 receptors 2. 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. 4395, Huang, R.Q.; Fang, M.J.; Dillon, G.H., Mol. Brain Res. 67: 177-183 (1999)<br></p>

<p>Stability Hygroscopic<br>Applications Urolithin A Glucuronide is a conjugate of Urolithin A acknowledged with in vivo anti-inflammatory and cancer chemopreventive properties.<br>References Gonzalez-Sarrias, A., et al.: J. Agric. Food Chem., 61, 4352 (2013); Gonzalez-Sarrias, A., et al.: Eur. J. Nutr., 56, 831 (2017)<br></p>

<p>Applications Hesperetin 3тАЩ-O-b-D-Glucuronide is one of the most abundant metabolite of Hesperetin (H289500) in vivo.<br>References van Zanden, J., et al.: Biochem. Pharmacol., 74, 345 (2007), Yanez, J., et al.: Biopharm. Drug Dispos., 29, 63 (2008), Brand, W., et al.: Drug Metab. Dispos., 38, 617 (2010),<br></p>

<p>Applications The cis isomer of human metabolite of Resveratrol (R150000).<br>References Athar, M., et al.: Toxicol. Appl. Pharmacol., 224, 274 (2007), Bernhardt, R., et al.: J. Biotechnol., 124, 128 (2006), Fairman, D.A., et al.: Drug Metab. Dispos., 35, 2159 (2007),<br></p>

<p>Stability Hygroscopic<br>Applications Quercetin 3-O-β-D-Glucuronide is a metabolite of Quercetin (Q509500).<br>References Ajay, M., et al.: Life Sci., 74, 603 (2003), Shen, S., et al.: Toxicol. Appl. Pharmacol., 197, 84 (2004), Amira, S., et al.: Eur. J. Pharmacol. 599, 126 (2008),<br></p>

<p>Applications Harpagoside is an iridoid glycoside along with with Harpagide (H105270), the potential to be strong anti-inflammatory agents providing the bulk of the observed effects from their plant origins.<br>References Zhang, L. et al.: Bioorg Med. Chem., 19, 4882 (2011); Wen, B. et al.: J. Ethnopharm., 147, 503 (2013);<br></p>

<p>Applications 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 Gulcan, H., et al.: Chem. Res. Toxicol., 21, 1503 (2008), Toropov, A., et al.: Bioorg. Med. Chem., 16, 5999 (2008), Franco, A., et al.: Envir. Toxicol. Chem., 28, 2018 (2009), Jensen, S., et al.: J. Agric. Food Chem., 57, 5872 (2009),<br></p>

<p>Applications BENZYL CINNAMATE (cas# 103-41-3) is a useful research chemical.<br></p>

<p>Applications 2,4,5-Trichlorophenol 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>Stability Light Sensitive, Temperature Sensitive<br>Applications A metabolite of cis Resveratrol.<br>References Schroder, H., et al.: Clin. Nutr., 20, 429 (2001), Yu, C., et al.: Pharm. Res., 19, 1907 (2002), Rimando, A., et al.: J. Agric. Food Chem., 52, 4713 (2004), Walle, T., et al.: Drug Metab. Dispos., 32, 1377 (2004), Ito, H., et al.: Br. J. Nutr., 94, 500 (2005),<br></p>