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Journal of Medicinal Chemistry|November 2, 1999
Structure-activity relationships at the monoamine transporters and sigma receptors for a novel series of 9-[3-(cis-3, 5-dimethyl-1-piperazinyl)propyl]carbazole (rimcazole) analoguesS M Husbands, S Izenwasser, T Kopajtic, et al.The Journal of Pharmacology and Experimental Therapeutics|August 17, 2000
BU48: a novel buprenorphine analog that exhibits delta-opioid-mediated convulsions but not delta-opioid-mediated antinociception in miceD C Broom, L Guo, A Coop, et al.Neuropharmacology|October 31, 2001
Rimcazole analogs attenuate the convulsive effects of cocaine: correlation with binding to sigma receptors rather than dopamine transportersR R Matsumoto, K L Hewett, B Pouw, et al.Combinatorial Chemistry & High Throughput Screening|April 3, 2001
Solid phase synthesis of 4-hydroxycinnamic acid and its derivatives for potential use in combinatorial chemistry: a novel route for the synthesis of 4-hydroxycinnamoyl coenzyme A and NMDA receptor antagonistsB G McIntyre, F Martínez Bermejo, S K Srivastava, et al.Journal of Medicinal Chemistry|January 22, 1998
Isothiocyanate derivatives of 9-[3-(cis-3,5-dimethyl-1-piperazinyl)propyl]carbazole (rimcazole): irreversible ligands for the dopamine transporterS M Husbands, S Izenwasser, R J Loeloff, et al.The Journal of Pharmacology and Experimental Therapeutics|August 17, 2000
Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamineJ H Broadbear, T L Sumpter, T F Burke, et al.Bioorganic & Medicinal Chemistry Letters|March 31, 2000
Probes for imidazoline binding sites: synthesis and evaluation of a selective, irreversible I2 ligandP A Coates, P Grundt, E S Robinson, et al.Drug and Alcohol Dependence|September 7, 2001
beta-carboline binding to imidazoline receptorsS M Husbands, R A Glennon, S Gorgerat, et al.Journal of Medicinal Chemistry|March 4, 2009
14 beta-O-cinnamoylnaltrexone and related dihydrocodeinones are mu opioid receptor partial agonists with predominant antagonist activityH Moynihan, A R Jales, B M Greedy, et al.Journal of Medicinal Chemistry|August 28, 1998
3-Alkyl ethers of clocinnamox: delayed long-term mu-antagonists with variable mu efficacyS M Husbands, J Sadd, J H Broadbear, et al.Pageof 3