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A highly selective kappa-opioid receptor agonist with low addictive potential and dependence liability
Hee Sock Park1, Hee Yoon Lee, Yong Hae Kim
1Department of Chemistry, KAIST, Daejeon 305-701, Republic of Korea.
Abstract:
Buprenorphine analogs have been synthesized. In the studies of analgesic and addictive effects in mice and [(35)S]GTPgammaS binding assay in human brain tissue, an analog of buprenorphine where the tert-butyl is replaced by a cyclobutyl moiety (16) has been identified as a selective kappa-partial agonist which gives antinociceptive effects, but has low abuse potential. The results may lead to lower degrees of dysphoria than full kappa-agonists.
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