Toxicologie

Stability Hygroscopic
Applications Troglitazone Sulfate is the major metabolite of Troglitazone (T892500), a hypoglycemic agent with cholestatic effect.
References Ciaraldi, T.P., et al.: Metabolism, 39, 1056 (1990); Kuzuya, T., et al.: Diabetes Res. Clin. Pract., 11, 147 (1991); Kellerer, M., et al.: Diabetes, 43, 447 (1994); Adachi, Y., et al.: Mol. Pharmacol., 67, 923 (2005);

Applications Labelled Ouabain (O714500). A cardiac glycoside that inhibits Na(+)/K(+) ATPase. It regulates transcription of MDR (increase, Pgp) and MRP (increase MRP1 and decrease CFTR, cyctic fibrosis transport receptor or cAMP-activated Cl- channel) genes, also alters localization of MRP1.
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 Padilha, A.S. et al.: Clin. Exp. Pharmacol. Physiol., 35, 801 (2008); Blaustein, M.P. et al.: Clin. Exp. Hypertens. 20, 691 (1998); van Huysse, J.W. et al.: Clin. Exp. Hypertens. 20, 657 (1998);

Applications 20-Deoxo-5-O-[3,6-dideoxy-3-(dimethylamino)-β-D-glucopyranosyl]-20-(1-piperidinyl)tylonolide is an intermediate in the synthesis of Tildipirosin (T440150), is a novel 16-membered-ring macrolide used in veterinary medicine.

Applications Diltiazem (D460620) intermediate (impurity B).
References Chaffman, M., et al.: Drugs, 29, 387 (1985), Kamath, B., et al.: J. Pharm. Biomed. Anal., 11, 407 (1993), Chankvetadze, B., et al.: J. Pharm. Biomed. Anal., 27, 161 (2002),

Stability Hygroscopic
Applications 4-Hydroxy Estrone 1-N7-Guanine is an estrogen metabolite formed with DNA which can lead to the mutations that initiate breast, prostate, and other types of cancer. Estrogen-DNA depurinating adducts as biomarkers of cancer risk and their use in cancer detection and prevention.
References Chakravarti, D., et al.: Mutat. Res., 456, 17 (2000), Liehr, J., et al.: Endocr. Rev., 21, 4054 (2000), Chakravarti, D., et al.: Oncogene, 20, 7945 (2001), Cavalieri, E., et al.: Chem. Res. Toxicol., 14, 1041 (2002),

Applications CRL-40,941 is a wakefulness-promoting agent. It was found to produce antiaggressive effects in animals.
References Lafon, L.: US4489095 (A) (1984)

Applications Fipexide Hydrochloride is one of five potential drug candidates to overcome the melphalan-induced vascular toxicity.
References Yang, Y., et al.: Tumour Biol., 37, 6709-6718 (2016);

Impurity Beclomethasone Dipropionate EP Impurity E
Applications 6α-Chlorobeclomethasone Dipropionate (Beclomethasone Dipropionate EP Impurity E) is an analogue of Beclomethasone Dipropionate (B131030), an antiallergic, antiasthmatic (inhalate). Anti-inflammatory (topical).
References Laube, B., et al.: J. Allergy Clin. Immunol., 101, 475 (1998); Harrison, L., et al.: Eur. J. Clin. Pharmacol., 58, 191 (2002); Maneechotesuwan, K., et al.: J. Allergy Clin. Immunol., 121, 43 (2008)

Applications Labelled Fenvalerate (F279450). An insecticide, used to control insects from food crops, animal feed and cotton products.
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 Sharma, R., et al.: Environ. Ecol., 27, 1481 (2009), Choudhary, S., et al.: J. Industrial Poll. Cont., 25, 145 (2009), Tang, J., et al.: Pest Man. Sci., 66, 121 (2010), Ai, G., et al.: J. Agric. Food Chem., 58, 694 (2010),

Applications Betamethasone 6α-Bromo 17-Valerate is an impurity of Betamethasone (B327000), which is a glucocorticoid used as an anti-inflammatory agent.
References Ferrante, M.G., et al.: Anal. Profiles Drug Subs., 6, 43 (1977), Li, A., et al.: Chem. Biol. Interact., 142, 7 (2002), Cruz-Monteagudo, M., et al.: Eur. J. Med. Chem., 40, 1030 (2005), Rothfuss, A., et al.: Chem. Res. Toxicol., 19, 1313 (2006),

Impurity Artemether USP Related Compound B
Applications Derivative of Artemisinin (A777500). Shows antimalarial and antifungal activity.
References Michael, O., et al.: Malaria J., 9, 335 (2010), Cesar, I., et al.: J. Pharm. Biomed. Anal., 54, 114 (2011), Galal, A. et al.: J. Nat. Prod. 68, 1274 (2005)

Applications A trizolopyrazine dipeptidyl peptidase IV inhibitor. It has recently been approved for the therapy of type II diabetes.
References Kim, D., et al.: J. Med. Chem., 48, 141 (2005), Ahren, B., et al.: Eur. J. Pharmacol., 521 164 (2005), Bergman, A., et al: Clin. Ther., 28, 55 (2006).

Applications (1R-cis)-Cyhalothric Acid is an intermediate in the synthesis of Bifenthrin (B383000), a third generation synthetic pyrethroid.
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 Faming Zhuanli Shenqing (2012), CN 102827004 A 20121219. Wei, W. J., et al.: Chirality., 22, 604 (2010);

Applications A diphenhydramine (D486900) analog classified as an antihistaminic.
References Bakker, R.A. et al.: Mol. Pharm., 60, 1133 (2001); Rekker, R.F. et al.: Arzneim.-Forsch., 21, 688 (1971);

Stability Hygroscopic
Applications Semisynthetic aminoglycoside antibiotic derived from Kanamycin A. Antibacterial.
References Cabana, T., et al.: Antimicrob. Agents Chemother., 3, 478 (1973), Cappelletti, L.M., et al.: J. Antibiot., 36, 328 (1983), Monteleone, P.M., et al.: Anal. Profiles Drug Subs., 12, 37 (1983),