Resolution and absolute configuration of an ergoline-related dopamine agonist, trans-4,4a,5,6,7,8,8a,9-octahydro-5-propyl-1H(or 2H)-pyrazolo[3,4-g]quinoline
- 1 August 1983
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 26 (8) , 1112-1116
- https://doi.org/10.1021/jm00362a005
Abstract
The title compound (.+-.)-5 (R = Pro) (LY141865) was resolved into a (-) isomer and a (+) isomer as the D- and L-tartrate salts, respectively. Dopamine agonist activity [rat striatal membranes] is a property of only the (-) isomer. Crystallographic analysis proved that the absolute configuration of the active (-) isomer is the same as that of the natural ergolines.This publication has 13 references indexed in Scilit:
- Inhibitory effects of pergolide on peripheral adrenergic neurotransmission in spontaneously hypertensive ratsLife Sciences, 1981
- Repeated administration of pergolide to rats attenuates the acute elevation of serum corticosterone by pergolidePharmacology Biochemistry and Behavior, 1981
- Stimulation of pre- and postsynaptic dopamine receptors by an ergoline and by a partial ergolineBrain Research, 1981
- Elevation of Serum Corticosterone Concentrations in Rats by Pergolide and Other Dopamine AgonistsEndocrinology, 1981
- Bicyclic and tricyclic ergoline partial structures. Rigid 3-(2-aminoethyl)pyrroles and 3- and 4-(2-aminoethyl)pyrazoles as dopamine agonistsJournal of Medicinal Chemistry, 1980
- BINDING OF [H-3]-LABELED PERGOLIDE MESYLATE TO DOPAMINE RECEPTORS OF MAMMALIAN BRAINS1980
- Role of hypothalamic dopaminergic receptors in the control of lordosis behavior in the female ratPhysiology & Behavior, 1979
- ASSAY OF 855 TEST CHEMICALS IN TEN TESTER STRAINS USING A NEW MODIFICATION OF THE AMES TEST FOR BACTERIAL MUTAGENS1979
- Effects of (8β)-8-[(Methylthio)methyl]-6-propylergoline on dopaminergic function and brain dopamine turnover in ratsLife Sciences, 1979
- Ergot alkaloids. Synthesis of 6-alkyl-8-ergolenes and 6-methyl-8-aminoergolines as potential prolactin inhibitorsJournal of Medicinal Chemistry, 1977