Flavonoïdes et Polyphénols

Stability Light Sensitive, Temperature Sensitive
Applications Xanthophyll is one of the most widespread carotenoid alcohols in nature. Originally isolated from egg yolk, also isolated by chromatography from nettles, algae, and petals of many yellow flowers.
References van het Hof, K., et al.: J. Nutr., 130, 503 (2000), Cooper, D., et al.: J. Nutr., 134, 221S (2004), Faulks, R., et al.: Biochim. Biophys. Acta, 1740, 95 (2005), Rao, A., et al.: Pharmacol. Res., 55, 207 (2007), Tuberoso, C., et al.: Food Chem., 103, 149 (2007),

Stability Hygrscopic
Applications α-Hederin is a saponin of dry extracts from the leaves of Hedera helix L.Inhibitor of β2-adrenergic receptor-GFP fusion proteins. Potential cause for asphyxiation.
References Sieben A. et al.: Biochem., 21, 3477 (2009); Gaillard, Y. et al.: J. Anal Toxicol., 27, 257 (2003);

Applications Curcumin β-D-Glucuronide Sodium Salt is the salt based analogue of Curcumin β-D-Glucuronide (C838510) which is a metabolite of Curcumin (C838500) in hepatic tissue and portal blood.
References Sharma, O., et al.: Biochem. Pharmacol., 25, 1811 (1976), Colletti, L., et al.: J. Clin. Invest., 85, 1936 (1990), Sharma, R., et al.: Clin. Cancer Res., 7, 1894 (2001),

Applications A bactericide detected in rivers and lakes. The current lot contains 8.7% d2, 0.2% d1 and 0.002% d0.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Lindstrom, A., et al.: Environ. Sci. Technol., 36, 2322 (2002)

Applications The aglucon of Naringin. Inhibitory mechanism of Naringenin against carcinogenic acrylamide formation and nonenzymic browning in Maillard model reactions.
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),

Stability Light Sensitive
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.
References Koh, T. et al.: In Vivo, 27, 85 (2013); Zhang, P. et al.: Arch. Pharm. Res., 36, 109 (2013);