Toxicologie

<p>Applications (+)-Irinotecan is a Topo I inhibitor.<br></p>

<p>Applications The active labelled metabolite of the antibacterial dye, Sulfamidochrysoidine. Inhibits folic acid synthesis in prokaryotes. Antibacterial.<br>References Colebrook, L., et al.: Lancet, 233, 1291 (1937), Dye, C., et al.: Nat. Rev. Microbiol., 7, 81 (2009), Isik, S., et al.: Bioorg. Med. Chem., 17, 1158 (2009),<br></p>

<p>Applications Bromothalonil can be used in biological study of comparison and validation of an in vitro skin sensitization strategy using a data set of 33 chemical references.Environmental toxin on US EPA Toxic Release Inventory list (TRI) list.<br>References Clouet, E., et al.: Toxicology In Vitro, (2017)<br></p>

<p>Applications 4’-Hydroxy Pyrimethanil is a labelled metabolite of the pesticide Pyrimethanil (P997250).<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 Environmental Protection Agency EPA: Fed. Reg., 69, 52434 (2004);<br></p>

<p>Applications A metabolite of Imipramine (I465980).<br>References Magdalou, J., et al.: J. Biol. Chem., 257, 13624 (1982), Orzechowski, A., et al.: Carcinogenesis, 15, 1549 (1994), Hawes, E., et al.: Drug Metab. Dispos., 26, 830 (1998),<br></p>

<p>Applications β-Cypermethrin is a pyrethroid compound that is used as an insecticide to eliminate unwanted pests from crop fields. β-Cypermethrin has been advertised to be safe for humans despite the fact that considered a possible 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 Chen, S., et al.: Appl. Micro. 94, 505 (2012); Li, Z., et al.: Bull. Env. Cont. Toxicol., 80, 335 (2008)<br></p>

<p>Applications Metyrapone acts as a glucocorticoid synthesis inhibitor, maintaining stress-hormone levels.<br>References Keller, C. et al.: Drug. Alc. Dep., 133, 405 (2013); Vilela, F. et al.: Neuroendocrinol., 97, 322 (2013);<br></p>

<p>Applications Main Quinfamide (Q670600) metabolite.<br>References Bailey, D., et al.: J. Med. Chem., 22, 599 (1979),<br></p>

<p>Applications Estradiol 17β-sulfate is a naturally occuring steroid in whihc can be converted into Estradiol(E888000)<br>References Takanashi, K., et al.: Steroids., 68, 383-392 (2003)<br></p>

<p>Applications Isovaleryl L-Carnitine-d3 Chloride is labelled Isovaleryl L-Carnitine Chloride (I917580) which is used to prepare carnitine benzyl esters as neuroprotectant prodrugs.<br>References Gong, X., et al.: J. Chem. Res., 6, 327 (2008)<br></p>

<p>Applications Metribuzin DK is a selective triazine herbicide used in the control of broadleaf weeds. Used in the protection of vegetable and fruit crops. Pesticide.<br>References Xie, Y. et al.: Microchem. J., 133, 468 (2017);<br></p>

<p>Applications Cymoxanil-d3 (methoxy-d3) (CAS# 2140803-92-3) is a useful isotopically labeled research compound of Cymoxanil(C988995). Cymoxanil is a fungicide applied as a seed treatment or as a foliar application to the plants to control late blight.<br>References Dhingani, J. C., et al.: J. Pure. App. Microbiol., 6, 1683 (2012); Bakirici, G.T., et al.: Food. Chem., 135, 1901 (2012);<br></p>

<p>Applications Diphenyl Phosphate is an organophosphate diester and metabolite of the flame retardant Triphenyl Phosphate (T808990) and also a metabolite of 2-Ethylhexyl diphenyl phosphate.<br>References Cooper, E.M. et al.: Anal. Bioanal. Chem., 401, 2123 (2011); Nishimaki-Mogami, T. et al.: Arch. Toxicol., 61, 259 (1988);<br></p>

<p>Applications Labelled acetylsalicylic acid impurity B.<br>References Walter, M., et al.: Eur. J. Biochem., 1996, 239, 281 (1996), Bantignies, B., et al.: Plant Mol. Biol., 42, 871 (2000), Bais, H., et al.: J. Biol. Chem., 278, 32413 ( 2003), Finkler, C., et al.: Genetica, 124, 117 (2005),<br></p>

<p>Applications 2'-O-Methyl Uridine-d3 is an isotope labelled compound of 2'-O-Methyl Uridine (M338200), a uridine analog used for the preparation of antiviral nucleoside derivatives as inhibitors of subgenomic hepatitis C virus RNA replication.<br>References Gratzner, H., et al.: Science, 218, 474 (1982), Jarvis, T., et al.: J. Biol. Chem., 271, 29107 (1996), Pavco, P., et al.: Clin. Cancer Res., 6, 2094 (2000),<br></p>