Results 121 to 130 of about 1,990 (193)
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Journal of the American Chemical Society, 1968
U Hornemann, H G Floss, Heinz G Floss
exaly +2 more sources
U Hornemann, H G Floss, Heinz G Floss
exaly +2 more sources
Synthesis of D-Oxa Tricyclic Partial Ergolines as Dopamine Agonists
Journal of Medicinal Chemistry, 1987J A Clemens, Edmund C Kornfeld
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Ergoline and non-ergoline derivatives in the treatment of Parkinson’s disease
Journal of Neurology, 2006There are a large variety of dopamine agonists available. Especially de novo patients are treated with dopamine agonists to avoid dyskinesia. Dopamine agonists can be subdivided into ergoline and non-ergoline derivatives. This distinction raises the question whether there are differences in the effects to treat symptoms, not only in the side effects ...
Heinz, Reichmann +6 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
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Stimulation of pre- and postsynaptic dopamine receptors by an ergoline and by a partial ergoline
Brain Research, 1981The capacity of the ergoline, pergolide, and of the partial ergoline, LY 141865, to stimulate pre- and postsynaptic dopamine (DA) receptors was investigated. Binding studies have revealed that pergolide has a high affinity, while the partial ergoline, LY 141865, has a low affinity for the postsynaptic striatal DA receptors in vitro.
J M, Rabey +4 more
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Serotonergic ergoline derivatives
Bioorganic & Medicinal Chemistry Letters, 1998Novel classes of 13- and 14-tertbutyl-ergoline derivatives were prepared, and characterised in vitro for their affinity for adrenergic, dopaminergic and serotonergic binding sites. This study particularly examines the importance of the presence and the position of the tert-butyl group in conferring either significant 5-HT1A or 5-HT2 affinity and ...
S, Mantegani +6 more
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Molecular Pharmacology, 1995
In this paper we show that a highly conserved aromatic residue, phenylalanine at the 340-position, is essential for ergoline binding to 5-hydroxytryptamine2A receptors. We hypothesized that F340 was essential for a specific aromatic-aromatic interaction (
M. S. Choudhary +5 more
semanticscholar +1 more source
In this paper we show that a highly conserved aromatic residue, phenylalanine at the 340-position, is essential for ergoline binding to 5-hydroxytryptamine2A receptors. We hypothesized that F340 was essential for a specific aromatic-aromatic interaction (
M. S. Choudhary +5 more
semanticscholar +1 more source
Chemischer Informationsdienst, 1986
AbstractErgolin‐thioharnstoffe (I) reagieren mit Acetylendicarbonsäureestern (II) zum Isomerengemisch der Ergolin‐thiazolidinone (III) und (IV).
K. SEIFERT, S. + HAERTLING, S. JOHNE
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AbstractErgolin‐thioharnstoffe (I) reagieren mit Acetylendicarbonsäureestern (II) zum Isomerengemisch der Ergolin‐thiazolidinone (III) und (IV).
K. SEIFERT, S. + HAERTLING, S. JOHNE
openaire +1 more source

