Bêta-bloquants

Applications A metabolite of labelled Diltiazem (D460620). References Shallcross, H., et al.: Br. Med. J., 295, 1236 (1987), Yeung, P.K.F., et al.: Drug Metab. Dispos., 18, 1055 (1990), Cashman, J.R., et al.: J. Med. Chem., 34,2049 (1991),

Applications Buflomedil is used as an vasodilator (peripheral). References Gundert-Remy, U., et al.: Eur. J. Clin. Pharmacol., 20, 459 (1981), Rosas, G., et al.: Angiology, 32, 291 (1981), Clissold, S.P., et al.: Drugs, 33, 430 (1987),

Applications Isotope labelled Difenacoum is a 4-hydroxycouramin derivative. Difenacoum is a second generation anticoagulant rodenticide used against rodent pests such as rats and mice. 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 Hadler, M.R. et al.: J. Hygiene, 74, 441 (1975); Rehman, A.B. et al.: J. Pharm., 1, 1 (1982); Quy, R.J. et al.: Crop Prot., 11, 14 (1992);

Applications di(2-Hydroxy Atorvastatin-d5) Calcium Salt is the labeled analogue of di(2-Hydroxy Atorvastatin) Calcium Salt (H828930), a metabolite of Atorvastatin Calcium Salt (A791750), a selective, competitive HMG-CoA reductase inhibitor. Atorvastatin is the only drug in its class specfically indicated for lowering both elevated LDL-cholesterol and triglycerides in patients with hypercholesterolemia. References Kearney, A.S., et al.: Pharm. Res., 10, 1461 (1993); Heinonen, T.M., et al.: Clin. Ther., 18, 853 (1996); Whitfield, L.R., et al.: Eur. J. Drug Metab. Pharmacokinet., 25, 97 (2000)

Applications A labelled nonsteroidal anti-inflammatory drug (NSAID); activity resides primarily in the (S)-isomer. References Busson, M., et al.: J. Int. Med Res., 14, 53 (1986), Meade, E.A., et al.: J. Biol. Chem., 268, 6610 (1993), Davies, N.M., et al.: Clin. Pharmacokinet., 34, 101 (1998),

Applications Cardioselective β-adrenergic blocker. Antihypertensive, antianginal, antiarrhythmic (class II). References Caplar, V., et al.: Anal. Profiles Drug Subs., 13, 1 (1984),

Applications A metabolite of Perhexiline. References Shah, R., et al.: Br. Med. J., 284, 295 (1982), Gould, B., et al.: Xenobiotica, 16, 491 (1986), Marquet, P., et al.: Ther. Drug Monit., 24, 255 (2002), Sallustio, B., et al.: Br. J. Clin. Pharmacol., 54, 107 (2002),

Applications Labelled Indapamide. Used as an antihypertensive. Diuretic. References Leary, et al.: Curr. Ther. Res., 15, 571 (1973), Kyncl, J., et al.: Arzneim.-Forsch., 25, 1491 (1975), DiFeo, T.J., et al.: Anal. Profiles Drug Subs. Excip., 23, 229 (1994),

Applications A labelled inhibitor of glucose synthesis. References Garcia-Salguero, L. et al.: Arch. Int. Physiol., Biochim. Biophys., 99, 237, (1991); Martirosyan, A., et al.: Biochem. Pharmacol., 68, 1729 (2004);

Heterocyclic compounds with oxygen hetero-atom(s) only

Labetalol hydrochloride (Sch-15719W), a salicylamide derivative, is a non-cardioselective blocker of β-adrenergic receptors and α1-adrenergic receptors.

Applications Tirofiban intermediate.

Applications Tienilic Acid is a heterocyclic derivative of phenoxyacetic acid. Tienilic acid is used as diuretic, uricosuric, antihypertensive. References Kerremans, A.L., et al.: Eur. J. Clin. Pharmacol., 22, 515 (1982), Manier, J.W., et al.: Am. J. Gastroenterol., 77, 401 (1982)