Several N-hetero aromatic compounds have been known to form dimers via oxidation and some of these to be in equilibrium with dissociated radicals. la-g
Dimerization of ergot derivatives
β Scribed by N.J. Bach; E.C. Kornfeld
- Book ID
- 104238238
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 94 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract Bromocriptine, lergotrile, lisuride, metergoline, and the Sandoz ergot derivatives 25β397, 29β712, and 29β717 have been tested for their ability to inhibit the synaptic receptor binding of spiroperidol, 5βhydroxytryptamine (5βHT), dβlysergic acid diethylamide (LSD), quinuclidinyl benzil
Studies of the effect of xanthines on the solubility of molecules related to the proteinaceous ergot alkaloids indicate the indole moiety to be a primary site for complexation. The tendency of indole and several analogs to form intermolecular complexes with caffeine was surveyed. This property leads