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Enantiomers of 11‐hydroxy‐10‐methylaporphine having opposing pharmacological effects at 5‐HT 1A receptors
Author(s) -
Can Joseph G.,
Moe Scott T.,
Long John Paul
Publication year - 1991
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.530030105
Subject(s) - enantiomer , chemistry , agonist , receptor , partial agonist , stereochemistry , pharmacology , biochemistry , medicine
The two enantiomers of the title compound have been prepared by different synthetic routes. Both bind strongly to 5‐HT 1A receptors from rat forebrain membrane tissue. However, in a guinea pig ileum preparation, the (R)‐enantiomer exhibits properties consistent with its being an agonist, whereas the (S)‐enantiomer shows no agonist effect, but it blocks the actions of the (R)‐enantiomer and of 8‐hydroxy‐2‐di‐ n ‐propylaminotetralin (8‐OH‐DPAT), a 5‐HT 1A agonist. These data are presented as a rare example of enantiomers which demonstrate opposite pharmacological effects at the same receptor.