Results 91 to 100 of about 2,032 (166)
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Conversion of ergolines to hexahydro- and octahydrobenzo[f]quinolines (depyrroloergolines).
Journal of Medicinal Chemistry, 1980A general method has been developed for removal of the pyrrole ring from the ergolines. Oxidation of various ergolines at the 2,3 double bond gave formamido ketones 10, which afforded the amino ketones 11.
N. Bach+3 more
semanticscholar +5 more sources
Ergot alkaloids. New ergolines as selective dopaminergic stimulants.
A new two-step sequence for the epimerization of methyl dihydrolysergate (5) at C-8 leading to methyl dihydroisolysergate (7) is presented. The latter compound was used as a starting material for the synthesis of various ergolines, of which (5R,8R,10R)-8-
P. Stütz+3 more
semanticscholar +2 more sources
Abstract The treatment of methyl lysergate with mercuric acetate in methanol yields, instead of the expected 10 - methoxy - 6 - methyl - ergoline - 8 β - carboxylic acid methyl ester (2), 10 - methoxy - 8,9 - didehydro - 6 - methyl - ergoline - 8 - carboxylic acid methyl ester (3), whose structure is demonstrated.
Luciano Bernardi+2 more
openalex +3 more sources
Abstract The preparation of the four isomeric methyl 10-methoxydihydrolysergates is reported. The configurations are assigned and the conformation of rings C and D is discussed. A mechanism for the formation of these 10-methoxy derivatives is suggested.
W. Barbieri+3 more
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Studies on the metabolism of ergoline derivatives
Abstract Tritium labelled nicergoline is rapidly absorbed from the gut in rat, dog, monkey and man. In the rat radioactivity was present in all tissues examined from 30 min to 12 hr after the administration. In all species tested labelled nicergoline was extensively metabolized in the body and the final products, labelled 1,6-dimethyl-8β ...
F Arcamone+4 more
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Experiences with a new ergoline (CF 25–397) in parkinsonism
Studies on rats with unilateral nigral lesions suggest that a new ergoline, CF 25-397, is a dopaminergic agonist that might improve parkinsonism. CF 25-397 induces less stereotyped behavior than other dopaminergic agents in rats, and might therefore cause less dyskinesia than levodopa in man.
Paul F. Teychenné+3 more
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ChemInform Abstract: Electrochemical Oxidation of Ergolines. [PDF]
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Karlheinz Seifert+2 more
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Preparation and Characterization of Ergoline Thiazolidinones and an Ergoline Imidazolidinone
Archiv der Pharmazie, 1986AbstractThe preparation of the ergoline thiazolidinones 2,3 and the ergoline imidazolidinone 5 is described. The 13C‐ and 15N‐NMR spectra of the 15N‐labelled compounds 15N‐ 2a and 15N‐3a allow the distinction of the two isomers.
Karlheinz Seifert+2 more
openaire +3 more sources
ChemMedChem, 2015
Ergolines were recently identified as a novel class of H3 receptor (H3R) inverse agonists. Although their optimization led to drug candidates with encouraging properties for the treatment of narcolepsy, brain penetration remained low.
Y. Auberson+14 more
semanticscholar +1 more source
Ergolines were recently identified as a novel class of H3 receptor (H3R) inverse agonists. Although their optimization led to drug candidates with encouraging properties for the treatment of narcolepsy, brain penetration remained low.
Y. Auberson+14 more
semanticscholar +1 more source
ChemInform Abstract: Serotonergic Ergoline Derivatives.
ChemInform, 1998AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Carla Caccia+6 more
openaire +4 more sources