1 emonstrating their ability to synthesize the opiate alkaloid.

2  form a functional common binding pocket for opiate alkaloids.

3 ertebrates via NO release as is the case for opiate alkaloids.

4  these cannabinoid actions resemble those of opiate alkaloids.

5 in FQ receptor based on the structure of the opiate alkaloids.

6  FQ receptor mutants can be labeled with the opiate alkaloid [3H]naltrindole and show greatly increas

7           The mu 3 receptor is selective for opiate alkaloids and is insensitive to opioid peptides.

8  pretreatment with N-nitro-L-arginine or the opiate alkaloid antagonist, naloxone.

9                                              Opiate alkaloids are potent analgesics that exert multip

10 n preserves the agonist/antagonist nature of opiate alkaloids as they interact with the mutant recept

11 ght into the cellular mechanisms involved in opiate alkaloid biosynthesis in opium poppy.

12 The parasitic worm Ascaris suum contains the opiate alkaloid morphine as determined by HPLC coupled t

13                 The levels of the endogenous opiate alkaloids morphine and codeine were significantly

14  are critical to its selectivity against the opiate alkaloids, particularly antagonists; and 2) mutat

15 ristics known to be unique to this receptor (opiate alkaloid selective and opioid peptide insensitive

16 icating that the process was mediated by the opiate alkaloid selective mu 3 receptor.

17 release may be mediated by activation of the opiate alkaloid-selective, opioid peptide-insensitive mi

18 h [(3)H]dihydromorphine further supports the opiate alkaloid selectivity and opioid peptide insensiti