Toxicology

<p>Applications Shows antioxidant effects. Antiseptic.<br>References Wong, S., et al.: Clin. Chem., 33, 214 (1987), Daood, H., et al.: Food Chem., 55, 365 (1996), Zainol, M., et al.: Food Chem., 81, 575 (2003),<br></p>

<p>Applications CP 55,940 is a cannabinoid agonist which is considerably more potent than Δ9-THC in both behavioral tests and receptor binding assays. Displays high and roughly equal affinity for both central and peripheral cannabinoid receptors (Ki = 0.6 - 5.0 and 0.7 - 2.6 nM at CB1 and CB2 respectively; EC50 values are 0.2, 0.3 and 5 nM at CB1, CB2 and GRP55 respectively).Controlled substance. Synthetic Cannabinoids<br>References Wiley, et al.: Neuropharmacology, 34, 669 (1995); Griffin, et al.: J. Pharmacol. Exp. Ther., 285, 553 (1998); Thomas, et al.: J. Pharmacol. Exp. Ther., 285, 285 (1998); Ryberg, et al.: Br. J. Pharmacol., 152, 1092 (2007);<br></p>

<p>Applications 7,8,9,10-Tetrahydro-8-methyl-6,10-methano-6H-pyrazino[2,3-h][3]benzazepine is a secondary amine drug varenicline impurity. It is a part of the pharmaceutical formulation of varenicline tartrate tablet.<br>References Waterman, K., et al.: J. Pharm. Sci., 97, 1499 (2008); Watheesh, B., et al.: Acta Chromatogr., 22, 207 (2010);<br></p>

<p>Applications A metabolite of Cevimeline (C283500).<br></p>

<p>Applications Labelled Isoproturon. Pre-and post-emergence herbicide for control of annual grasses and broad-leaved weeds. Herbicide.<br>References Fournier, J.-C., et al.: Chemosphere, 4, 207 (1975), Gonzales, P., et al.: Weed Res., 23, 39 (1983),<br></p>

<p>Applications N-Deethoxymethyl Chlorfenapyr is a primary metabolite of Chlorfenapyr (C428500). Chlorfenapyr is a halogenated pyrrole based pro-insecticide. Chlorfenapyr functions by metabolizing into an active insecticide after entering the host. Chlorfenapyr is used primarily as a means of pest control on cotton.<br>References Lovell, J.B. et al.: Bright. Crop Prot. Pests Dis., 1, 37 (1990); Wier, A.T. et al.: J. Agric. Entemol., 11, 311 (1994); Black, B.C. et al.: Pest. Biochem. Physiol., 50, 115 (1994); Albers, P. H., et al.: Environ. Toxicol. Chem., 25, 438 (2006)<br></p>

<p>Applications Isotope Labelled 1-Cyclopropyl-8-ethoxy-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid is an impurity in the synthesis of Moxifloxacin (M745000), a fluorinated quinolone antibacterial.<br>References Woodcock, J.M., et al.: Antimicrob. Ag. Chemother., 41, 101 (1997), Stass, H., et al.: Antimicrob. Ag. Chemother., 42, 2060 (1998)<br></p>

<p>Applications Labelled trans-Hydroxy Praziquantel (H952405). The main cis-monohydroxylated metabolite of Praziquantel (P702095).<br>References Buehring, K., et al.: Eur. J. Drug Metab. Pharm., 3, 179 (1978), Moldeus, P., et al.: Methods Enzymol., 52, 60 (1978), Cioli, D., et al.: Pharmacol. Ther., 68, 35 (1995),<br></p>

<p>Applications Pipobroman-D8 is a labelled analogue of Pipobroman (P490602).<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 (S)-7-Hydroxy Efavirenz, is a metabolite of Efavirenz (E425000), a nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiviral.<br>References Young, S.D., et al.: Antimicrob. Ag. Chemother., 39, 2602 (1995),<br></p>

<p>Applications Labelled (6R,7S)-Cefoperazone (C242890). (6R,7S)-Cefoperazone is the enantiomer of Cefoperazone (C242900) as an impurity.<br>References Fabre, H., et al.: J. Pharm. Sci., 73, 611 (1984), Strasters, J., et al.: Anal. Chem., 63, 2503 (1991), Chen, Z., et al.: World Notes Antibiot., 25, 249 (2004),<br></p>

<p>Applications Prometryn-d14 (di-iso-propyl-d14) (CAS# 1202864-57-0) is a useful isotopically labeled research compound.<br></p>

<p>Applications 4-Methoxy-n,6-dimethyl-1,3,5-triazin-2-amine is a metabolite of tribenuron-methyl used in herbicidal formulations or used as herbicides.<br>References Bhattacherjee, A. K., et al.: Biomed. Chromatogr., 12, 196 (1998)<br></p>

<p>Applications A pigment that forms during the visual cycle in vertebrates leading to harmful byproducts of this biosynthetic pathway.<br>References Anderson, R., et al.: Biochem., 9, 3624 (1970), Liu, J., et al.: J. Biol Chem., 38, 29354 (2000)<br></p>

<p>Applications Dimension can be employed as a herbicide.<br>References Zhang, R., et al.: Sepu., 36, 1228-1237 (2018)<br></p>

<p>Applications Erythromycin Ethyl Succinate-13C,d3 is the deuterated form of Erythromycin Ethyl Succinate (E649985), which is a derivative of Erythromycin (E649950), an antibiotic.<br>References Koch, W.L., et al.: Anal. Profiles Drug Subs., 8, 157 (1979); Serisier, D. et al.: J. Am. Med. Assoc., 309, 1206 (2013);<br></p>

<p>Applications Protected metabolite of Mycophenolic Acid.<br>References Nelson, P., et al.: J. Med. Chem., 39, 4181 (1996), Ubukata, M., et al.: Bioorg. Med. Chem. Lett., 17, 4767 (2007),<br></p>