Alcaloidi oppiacei

Applications Labelled Oxycodone. Controlled substance (opiate). Analgesic (narcotic).
References Mendelson, J., et al.: Clin. Pharmacol. Ther., 60, 105 (1996), Fudala, P., et al.: N. Engl. J. Med., 349, 949 (2003), Alho, H., et al.: Drug Alcohol Depend., 88, 75 (2007),

Applications: (R)-Apomorphine-11-sulfate Potassium Salt-d5 is the isotope labelled analog of (R)-Apomorphine-11-sulfate Potassium Salt (A727520); a derivative of (R)-Apomorphine (A727500) which is a dopamine (D1 and D2) receptor agonist, emetic, and antiparkinsonian.
References Neumeyer, J.L., et al.: J. Pharm. Sci., 59, 1850 (1970); Ginos, J.Z., et al.: J. Med. Chem., 18, 1194 (1975); Muhtadi, F.J., et al.: Anal. Profiles Drug Subs., 20, 121 (1991)

Applications Labelled Hydrocodone. Analgesic (narcotic); antitussive.Controlled substance (opiate).
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 Eddy, N.B., et al.: J. Pharmacol. Exp. Ther., 52, 468 (1934), Stein, A., et al.: Pharmazie, 10, 180 (1955), Peer, C., et al.: J. Anal. Toxicol., 31, 515 (2007),

Applications L-Propoxyphene-d5 Hydrochloride is the isotope labelled analog and L-isomer of Propoxyphene Hydrochloride (P831500); a controlled substance (opiate) and analgesic (narcotic). The α-DL-and D-diastereoisomers possess marked analgesic activity in contrast to the β-diastereoisomers which are substantially inactive. Oral administration of L-Propoxyphene Hydrochloride enhances the analgesic activity of D-Propoxyphene Hydrochloride.
References Goldenthal, E.I., et al.: Toxicol. Appl. Pharmacol., 18, 185 (1971); McEwan, B., et al.: Anal. Profiles Drug Subs., 1, 301 (1972); Murphy, P.J., et al.: J. Pharmacol. Exp. Ther., 199, 415 (1976)

Applications (S)-Moramide or Dextromoramide is a controlled substance (opiate). Analgesic (narcotic).
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 Aoyama, T., et al.: J. Pharm. Sci., 79, 465 (1990); Decamp, W., et al.: J. Pharm. Biomed. Anal., 11, 1167 (1993);