Synthesis and opioid activities of some naltrexone oxime ethers
…, PV Kaplita, DL DeHaven-Hudkins
Index: Mavunkel, B. J.; Rzeszotarski, W. J.; Kaplita, P. V.; DeHaven-Hudkins, D. L. European Journal of Medicinal Chemistry, 1994 , vol. 29, # 9 p. 659 - 666
Full Text: HTML
Citation Number: 8
Abstract
Abstract A series of alkyl, cycloalkyl, aryl, and aralkyl ethers of naltrexone oxime was prepared. The compounds were examined in binding assays for μ, δ and κ opioid receptor affinity. In addition, the, naltrexone oxime ethers were studied in animal models that measure opioid agonist and antagonist activity. These studies led to the discovery of several compounds, notably phenethyl 3e and phenylpropyl 3f ethers of naltrexone, which have a ...
Related Articles:
[Kim, Dae-Kee; Gam, Jongsik; Kim, Young-Woo; Lim, Jinsoo; Kim, Hun-Taek; Kim, Key H. Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2363 - 2373]
[Kim, Dae-Kee; Gam, Jongsik; Kim, Young-Woo; Lim, Jinsoo; Kim, Hun-Taek; Kim, Key H. Journal of Medicinal Chemistry, 1997 , vol. 40, # 15 p. 2363 - 2373]
Derivatives of hydroxylamine: central nervous system stimulants
[Major,R.T.; Ohly,K.W. Journal of Medicinal and Pharmaceutical Chemistry, 1961 , vol. 4, p. 51 - 65]