Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine

JH Broadbear; TL Sumpter; TF Burke; SM Husbands; JW Lewis; JH Woods; JR Traynor

Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine

JH Broadbear
, TL Sumpter
, TF Burke
, SM Husbands
, JW Lewis
, JH Woods
, JR Traynor

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

Translated title of the contribution	Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine
Original language	English
Pages (from-to)	933 - 940
Journal	Journal of Pharmacology and Experimental Therapeutics
Volume	294
Publication status	Published - 2000

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@article{f639d0a183c448438e53268200fa6440,

title = "Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine",

author = "JH Broadbear and TL Sumpter and TF Burke and SM Husbands and JW Lewis and JH Woods and JR Traynor",

year = "2000",

language = "English",

volume = "294",

pages = "933 -- 940",

journal = "Journal of Pharmacology and Experimental Therapeutics",

issn = "1521-0103",

publisher = "Elsevier Inc.",

}

Broadbear, JH, Sumpter, TL, Burke, TF, Husbands, SM, Lewis, JW, Woods, JH & Traynor, JR 2000, 'Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine', Journal of Pharmacology and Experimental Therapeutics, vol. 294, pp. 933 - 940.

Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine. / Broadbear, JH; Sumpter, TL; Burke, TF et al.
In: Journal of Pharmacology and Experimental Therapeutics, Vol. 294, 2000, p. 933 - 940.

Research output: Contribution to journal › Article (Academic Journal) › peer-review

TY - JOUR

T1 - Methocinnamox is a potent, long-lasting, and selective antagonist of morphine-mediated antinociception in the mouse: Comparison with clocinnamox, beta-funaltrexamine, and beta-chlornaltrexamine

AU - Broadbear, JH

AU - Sumpter, TL

AU - Burke, TF

AU - Husbands, SM

AU - Lewis, JW

AU - Woods, JH

AU - Traynor, JR

PY - 2000

Y1 - 2000

M3 - Article (Academic Journal)

SN - 1521-0103

VL - 294

SP - 933

EP - 940

JO - Journal of Pharmacology and Experimental Therapeutics

JF - Journal of Pharmacology and Experimental Therapeutics

ER -