In vitro biotransformation of the analgesic agent, RWJ-51784, in rat, dog and human

Author:

Wu W. N.,McKown L. A.,Carson J. R.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Reference10 articles.

1. Ruffolo, R. R., Bondinelli, W., Hieble, J. P., (1995): α- and β-Adrenoceptors: from the gene to the clinic, 2. structure-activity relationships and therapeutic applications. J. Med. Chem. 38(18), 3681.

2. Reitz, A. B., Carson, J. R., Boyd, R. E., Pitis, P. M., Jetter, M. C., Baxter, E. W., McDonnell, M. E., Ross, T. M., Connelly, C. D., Lewis, M. and Codd, E. E., (1999): Alpha-2 adrenoceptor agonists for the treatment of pain, (Abstract # MEDI-158, The 217th ACS National Meeting).

3. Carmosin, R. J., Carson, J. R. and Pitis, P. M., (1999): Preparation of octahydropyrrolo-[3,4-c]carbazoles useful as analgesic agents, US Patent No. 6063803.

4. Vaught, J. L., Carson, J. R., Carmosin, R.J., Blum, P. S., Persico, F. J., Hageman, W. E., Shank, R. P. and Raffa, R. B., (1990): Antinociceptive action of McN-5195 in rodents: a structurally novel (indolizine) analgesic with a nonopioid mechanism of action. J. Pharmacol. Exp. Ther., 255(1), 1–10.

5. Vaught, J. L. and Raffa, R. B., (1991): Centrally-mediated antinociceptive action of RWJ-22757 (formerly McN-5195): involvement of spinal descending inhibitory pathways (an hypothesis) Life Sci., 48(23), 2233–41.

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