Buprenorphine is a widely used analgesic. Its in vivo properties are partial agonism at
μ-receptors and antagonism at κ-receptors. For the investigation of the role of the
tertiary alcohol function in the pharmacology of buprenorphine, a series of ring
constrained analogues of buprenorphine, in which the tertiary hydroxyl substituent on
C19 is fixed in different positions either above (BU46 and BU95) or below (BU47,
BU96, BU48 and BU61) the plane of the ring, have been studied in several biological
test systems, include binding assays, isolated tissue bioassays and intracellular assays. [Continues.]
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Publication date
1996
Notes
A Master's Thesis. Submitted in partial fulfilment of the requirements for the award of Master of Philosophy at Loughborough University.