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J H Broadbear

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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.

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.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 13 results.

The Journal of Pharmacology and Experimental Therapeutics|August 17, 2000

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.

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