Flavonoidi e Polifenoli

<p>Applications (E)-Neochlorogenic Acid is an antioxidant compound used in the treatment of oxidative stress and related afflictions.<br>References Wang, J. et al.: Molecules, 19, 21226 (2014); Jimenez-Zamora, A. et al.: LWT-Food Sci. Tech., 61, 12 (2015);<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>

<p>Stability Hygroscopic, Light Sensitive<br>Applications Erythrosine B Disodium Salt is a derivative of fluorone and is used as a cherry-pink synthetic colour additives used on food products. Dyes and metabolites, Environmental Testing<br>References Xue, H., et al.: Adv. Mat. Res., 476, 2239 (2012); Harp, B. P., et al.: Food. Add. Contamin., 29, 886 (2012); Sarikaya, R., et al.: Chemosphere., 88, 974 (2012);<br></p>

<p>Applications Naturally occurring flavonic glycoside; rhamnoglycoside of Diosmetin. Capillary protectant.<br>References Damon, M., et al.: Arzneim.-Forsch., 37, 1149 (1987), Laurent, R., et al.: Int. Angiol., 7, 39 (1988), Tajana, A., et al.: Minerva Med., 79, 387 (1988),<br></p>

<p>Applications Pinocembrin is a flavanoid with antioxidant activity found in damiana, honey, and propolis. Recent studies show that Pinocembrin maybe be a therapeutic option in reducing cerebral ischemia/reperfusion injury as a result of its anti-oxidative and anti-apoptotic effects. Pinocembrin displayed neuroprotective effects in glutamate injury model partly by inhibiting p53 expression causing a lower Bax-Bcl-2 ratio and by inhibiting the release of cytochrome c.<br>References Zhao, J. et al.: J. Ethnopharmacol., 120, 387 (2008); Liu, R. et al.: Brain Res., 1216, 104 (2008); Gao, M. et al.: Eur. J. Pharmacol., 591, 73 (2008);<br></p>

<p>Applications 18α-Glycyrrhetinic Acid 3-O-β-D-Glucuronide is a metabolite of 18α-Glycyrrhetinic Acid (G735005), an anti-inflammatory which also rapidly and reversibly blocks gap junction intercellular communication (GJIC).<br>References Guo, Y., et. al.: Am. J. Phys.: 276, L1018 (1999)<br></p>

<p>Applications Isotope labelled Triclosan is used as bactericide and preservative for cosmetic and detergent compositions (1). Broadly used as an antiseptic and disinfectant (2). This compound is a contaminant of emerging concern (CECs). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA). Environmental contaminants; Food contaminants.<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 1. Lindström, A. et al.: Environ. Sci. Technol. 2002 Jun 1;36(11):2322-9. 2. Ruszkiewicz, J. et al.: J. Toxicol. Environ. Health B. Crit. Rev. 2017;20(2):104-117.<br></p>

<p>Applications Minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression.<br>References Powell, R.G., et al.: Phytochemistry, 35, 335 (1994), Jeandet, P., et al.: J. Phytopathol., 143, 135 (1995), Mattivi, F., et al.: J. Agric. Food Chem., 43, 1820 (1995),<br></p>

<p>Applications Scopoletin is the aglucone of Scopolin. Used for cosmetics, topical formulations, and foods. Dyes and metabolites.<br></p>

<p>Stability Hygroscopic<br>Applications Eupatilin maintains anticoagulant and antiplatelet activity isolated from the Artemisia princeps Pampanini flower.<br>References Ryu, R. et al.: Prev. Nutr. Food Sci., 18, 181 (2013);<br></p>

<p>Stability Hygroscopic, Light Sensitive<br>Applications 13C-labelled Phenol (P318000).<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></p>

<p>Applications Methyleugenol is a phenylpropene that is commonly found in plants such as nutmeg, pimento, lemongrass, tarragon, basil, star anise, and fennel. Methyleugenol has been shown to inhibit histone deacetylase (HDAC) activity in the human colon carcinoma cell line HT29. Compounds that exhibit HDAC-inhibitory properties or disrupt the HDAC complex have potential applications in cancer therapy and chemoprevention. In addition, Methyleugenol is a flavoring agent often used in consumer products such as jellies, baked goods, beverages,chewing gums, ice cream, and fragrance.<br>References Groh, I. A., et al.: J Nutr Metab. 2013, 821082 (2013); R. L. Smith, et al.: Food Chem Toxicol 40, 851 (2002)<br></p>

<p>Applications Carnosic Acid is a phenolic component of rosemary. It acts as a potent antioxdant and also has UV protective activity. Specifically protection for UV-A radiation and damage. Carnosic Acid also inhibits the free-radical chain reaction that leads to the oxidation of fats and oils, thereby stabilizing and increasing the shelf life of meats.<br>References Frankel, E. et al.: J. Agri. Food Chem., 44, 131 (1996); Offord, E. et al.: Free Rad Biol. Med., 32, 1293 (2002); Chem. and Eng. News Feb. 10, 2014 p. 13<br></p>

<p>Applications Labelled Chloroxylenol. Chloroxylenol is an antiseptic and germicide. Chloroxylenol is used for mildew prevention. Chloroxylenol is also an antibacterial.<br>References Heberer, T., et al.: Toxicol. Lett., 131, 5 (2002); Nikolaou, A., et al.: Anal. Bioanal. Chem., 387, 1225 (2007); Focazio, M., et al.: Sci. Total Environ., 402, 201 (2008); Miege, C., et al.: Environ. Pollut., 157, 1721 (2009);<br></p>

<p>Impurity Diosmin EP Impurity D<br>Applications 6-Iodo Diosmin (Diosmin EP Impurity D) is a Diosmin (D485200) impurity.<br></p>

<p>Stability Light Sensitive<br>Applications Labelled Tyrosol (T947800) metabolite.<br>References Perez-Trujillo, M., et al.: J. Agric. Food Chem., 58, 9129 (2010), Gregus, P., et al.: J. Pharm. Biomed. Anal., 53, 674 (2010), Garcia-Villalba, R., et al.: Anal. Bioanal. Chem., 398, 463 (2010),<br></p>

<p>Applications Anisole is used in perfumery.<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 Taylor, J.M., et al.: Toxicol. Appl. Pharmacol., 6, 378 (1964),<br></p>

<p>Applications Silydianin is an active constituent of Silybium marianum and is known the exhibit anti-inflammatory activity which regulates caspase-3 activation which affects cell membranes and acts as a free radical scavenger.<br>References Zlelinska-Przyyjemska, M., et al.: Phytother. Res., 20, 115 (2006); Milan, M., et al.L Anal. Chimica. Acta., 486, 125 (2003); Liu, Y.Z., et al.: Chin. Herb. Med., 4, 237 (2012);<br></p>

<p>Applications An isoflavone with anticancer proliferation, differentiation and chemopreventitive properties. Inhibits metabolic activation of benzo[a]pyrene.<br>References Chae, Y.H., et al.: Chem. Biol. Interactions, 82, 181 (1992), Jing, Y. and Waxman, S.: Anticancer Res., 15(4), 1147 (1995)<br></p>

<p>Applications Isovitexin is known as a flavones, a class of flavonoids. Isovitexin have been studied for their antiradical activities in the process of metabolisms. Isovitexin have also been studied for beneficial effcts against atherosclerosis, osteoporosis and certain cancers.<br>References Cermak, R., et al.: Expert. Opin. Drug. Metab. Toxicol., 4, 17 (2008); Ma, X., et al.: J. Agri. Food. Chem., 60, 10844 (2012); Li, H., et al.: Food. Chem., 135, 2942, (2012);<br></p>

<p>Stability Hygroscopic<br>Applications (-)-Riboflavin is a nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, leafy vegetables. Richest natural source is yeast. Minute amounts present in all plant and animal cells. Vitamin (enzyme cofactor).<br>References Unna, K., et al.: J. Pharmacol. Exp. Ther., 76, 75 (1942), Rivlin, et al.: N. Engl. J. Med., 283, 463 (1970), Al-Shammary, F.J., et al.: Anal. Profiles Drug Subs., 19, 429 (1990),<br></p>

<p>Applications The demethoxy derivative of Curcumin (C838500) that regulates anti-inflammatory and anti-proliferative responses through a ROS-independent mechanism. It attenuates the Wnt/β-catenin pathway through down-regulation of the transcriptional coactivator p300.<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 Ryu, M.J. et al.: Biochem. Biophys. Res. Comm., 377, 1304 (2008); Sandur, S.K. et al.: Carcinogenesis, 28, 1765 (2007); Huang, T. et al.: J. Agric. Food. Chem., 58, 10639 (2010);<br></p>

<p>Applications Triclosan O-β-D-Glucuronide is a metabolite of the bacteriostat, 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>Applications A human metabolite of Resveratrol (R150000). Piceatannol is strong anti-oxidant.<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>Applications A metabolite of Apigenin. Antibacterial. Metabolite of Luteolin in rats.<br>References Baylocq, D., et al.: Ann. Pharm. Fr., 41, 115 (1983), Allen, S., et al.: Drug Metab. Dispos., 29, 1074 (2001), Birt, D., et al.: Pharmacol. Ther., 90, 157 (2001), Boersma, M., et al.: Chem. Res. Toxicol., 15, 662 (2002); Chen, Z., et al.: Drug Metab. Dispos., 39, 667 (2011)<br></p>

<p>Applications Urolithin M6 is an intestinal microbial metabolite of ellagitannins.<br>References Garcia-Villalba, R., et al.: J. Agr. Food Chem., 61, 8797 (2013);<br></p>

<p>Applications The compund shows an anti-cancer activity, plasma cholesterol reduction, reduction in postmenopausal bone loss.<br>References Whalley, J.L., et al.: Bioorg. Med. Chem. Lett., 8, 1569 (1998), Song, T., et al.: J. Agric. Food Chem., 47, 1607 (1999),<br></p>

<p>Stability Light Sensitive<br>Applications Labelled Eugenol is a dental compound which shows cytotoxicity to human oral squamous cell carcinoma and oral cells. When glucosylated, this compound exhibits anti-inflammatory activity.<br>References Koh, T. et al.: In Vivo, 27, 85 (2013); Zhang, P. et al.: Arch. Pharm. Res., 36, 109 (2013);<br></p>

<p>Applications Thiochrome is a selective M4 muscarinic receptor enhancer of acetylcholine affinity.<br>References Mohsen, Z., et al.: Food and chemical toxicology, 49 (2011); Lazareno, S., et al.: Molecular pharmacology, 65 (2004);<br></p>

<p>Applications A bactericide detected in rivers and lakes. The current lot contains 8.7% d2, 0.2% d1 and 0.002% d0.<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 Lindstrom, A., et al.: Environ. Sci. Technol., 36, 2322 (2002)<br></p>

<p>Applications The aglucon of Naringin. Inhibitory mechanism of Naringenin against carcinogenic acrylamide formation and nonenzymic browning in Maillard model reactions.<br>References Lomovskaya, N., et al.: J. Bacteriol., 181, 305 (1999), Chung, L., et al.: J. Antibiot., 54, 250 (2001), Kim, D., et al.: Biochemistry, 43, 981 (2004), Kumar, S., et al.: J. Biol. Chem., 280, 19569 (2005),<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>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 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>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>

<p>Applications 1,5-Dicaffeoylquinic Acid acts as an anti-hyperlipidemic agent. In addition, acts as a neuroprotective agent against amyloid-β toxicity in the treatement of Alzheimer’s.<br>References Gray, N. et al.: J. Alz. Dis., 40, 359 (2014); Liu, H. et al.: J. App. Pharm. Sci., 3, 016 (2013);<br></p>

<p>Applications An antioxidant flavenoid.<br>References Dixon, D., et al.: J. Biol. Chem., 285, 36322 (2010), Sheu, M., et al.: Chem. Pharm. Bull., 58, 1187 (2010),<br></p>

<p>Applications 2,4,6-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>References Nunes, C., et al.: J. Env. Biol., 29, 733 (2008), Carucci, A., et al.: Water Sci. Technol., 58, 309 (2008), Fu, W., et al.: Env., Toxicol., Chem., 28, 1372 (2009), Osborne, R., et al.: Biochem., 48, 4231 (2009), Campoy, S., et al.: Env. Microbiol., 11, 99 (2009),<br></p>

<p>Applications Urolithin M5 is an intestinal microbial metabolite of ellagitannins.<br>References Garcia-Villalba, R., et al.: J. Agr. Food Chem., 61, 8797 (2013);<br></p>

<p>Applications An anthocyanin responsible for red pigment in fruits and berries. It is an antioxidant, protecting the cell against damage from SOD.<br>References Riihinen, K., et al.: Food Chem., 110, 156 (2008), Khanizadeh, S., et al.: J. Food Comp. Anal., 21, 396 (2008), Viskelis, P., et al.: J. Food Sci., 74, C157 (2009), Comeskey, D., et al.: J. Agric. Food Chem., 57, 2035 (2009),<br></p>

<p>Applications Silybin B is the 2R, 3R, 7‘S, 8‘S isomer of Silybin (S465850); a natural occurring flavolignan that exerts anti-inflammatory and anti-fibrogenic effects on human hepatic stellate cells.<br>References Lee, D.Y.W, et al.: J. Nat. Prod., 66, 1171 (2003); Trappoliere, M., et al.: J. Hepatol., 50, 1102 (2009); Borsari, M., et al.: J. Inorg. Biochem., 85, 123 (2001)<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>Impurity Diosmin EP Impurity E<br>Stability Hygroscopic<br>Applications Linarine (Diosmin EP Impurity E) is a naturally occurring flavone glycoside that was identified to possess potential sedative and anticonvulsant properties.<br>References Nugroho, A., et al.: Arch. Pharma. Res., 36, 51 (2013); Jung, H.A., et al.: Arch. Pharma. Res., 35, 1021 (2012); Shen, H.J., et al.: J. Med. Plants. Res., 5, 6555 (2011);<br></p>

<p>Applications Sulfuric Acid conjugated Genistein metabolite.<br>References Kinjo, J., et al.: Biol. Pharm. Bull., 27, 185 (2004), Tsuchihashi, R., et al.: Nat. Med., 58, 71 (2004), Bursztyka, J., et al.: Food Chem. Toxicol., 46, 939 (2008),<br></p>

<p>Applications Allyl Bromide is used as a reagent in the synthesis of Resveratrol derivatives. Resveratrol (R150000) is a minor constituent of wine, correlated with serum lipid reduction and inhibition of platelet aggregation. Resveratrol is a specific inhibitor of COX-1, and it also inhibits the hydroperoxidase activity of COX-1. It has been shown to inhibit events associated with tumor initiation, promotion and progression.<br> E0<br>References Powell, R.G., et al.: Phytochemistry, 35, 335 (1994), Jeandet, P., et al.: J. Phytopathol., 143, 135 (1995), Mattivi, F., et al.: J. Agric. Food Chem., 43, 1820 (1995); Mulakayala, C. et al.: J. Mol. Graph. Model., 41, 43 (2013);<br></p>

<p>Applications Hexahydrocurcumin-d6 is an isotope labelled degradation product of Curcumin (C838500), a dietary anti-inflammatory and chemopreventive agent consisting of two methoxyphenol rings connected by a conjugated heptadienedione chain.<br>References Gordon, D.N., et al.: J. Biol. Chem., 290, 4817 (2015);<br></p>

<p>Applications Imperatorin (cas# 482-44-0) is a compound useful in organic synthesis.<br></p>

<p>Applications tBHQ is an antioxidant in induction of AP-1, NF-κB, and glutathione S-transferase gene expression. It also disrupts ability of Kelch-like ECH-associated protein 1(Keap1) to target Nrf2, a bZIP transcription factor, for proteasome-mediated degradation and promote nuclear accumulation of Nrf2.<br>References Pinkus, R., et al.: J. Biol. Chem., 271, 13422 (1996); Zhang, D., et al.: Mol. Cell. Bio., 23, 8137 (2003)<br></p>

<p>Applications Narcissoside is a flavonoid from Nitraria tangutorum. Narcissoside may have antiproliferative activity in human colon cancer cell line (HT29).<br>References Wu, Z., et. al.: Chem. Nat. Compnd., 49, 1125 (2014); Serra, A.T., et. al.: Food Res. Int., 54, 892 (2013)<br></p>

<p>Applications A metabolite of trans Resveratrol (150000).<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>