Results 131 to 140 of about 1,990 (193)
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Partial dopamine-agonistic and atypical neuroleptic properties of the amino-ergolines SDZ 208-911 and SDZ 208-912.

Journal of Pharmacology and Experimental Therapeutics, 1990
The aminoergolines SDZ 208-911 [N-[(8-alpha)-2,6-dimethylergoline-8-yl]-2,2- dimethylpropanamide] and SDZ 208-912 [N-[8-alpha)-2-chloro-6-methylergoline-8-yl]- 2,2-dimethylpropanamide] exhibit nonclassical, neuroleptic-like properties in rodents.
D. Coward   +6 more
semanticscholar   +1 more source

Electrochemical Oxidation of Ergolines

Helvetica Chimica Acta, 1992
AbstractAn electrochemical procedure for the preparation of D‐3‐alkoxy‐halogen‐2,3‐dihydro‐6‐methyl‐2‐oxoergolines‐I is described.
Karlheinz Seifert   +2 more
openaire   +1 more source

Serotonin-induced contraction in porcine coronary artery: use of ergolines to support vascular 5-hydroxytryptamine2-receptor heterogeneity.

Journal of Pharmacology and Experimental Therapeutics, 1993
Serotonin-induced contraction in porcine coronary artery was studied in ring segments of coronary artery without endothelium. 5-hydroxytryptamine (5-HT), 5-methoxytryptamine (5-MeOT) and alpha-methyl-5-HT (alpha Me-5-HT) concentration-dependently ...
D. Cushing, M. Cohen
semanticscholar   +1 more source

A Crystallographic Investigation of Ergolines

Structural Chemistry, 2002
The X-ray crystal structures of three ergoline derivatives have been completed and are reported herein. These include mesulergine hydrochloride (III), pergolide methanesulfonate (IV), and dihydroergocriptine hydrate (V). These molecules show dopamine agonist activity at the D2 receptor.
Naijue Zhu   +3 more
openaire   +1 more source

Ergoline derivatives—VIII

Tetrahedron, 1965
Abstract The NH region of the IR spectra of lysergamides and dihydrolysergamides are reported, discussed and the bands assigned. Axial and equatorial amides are clearly distinguishable, the former present between the amide hydrogen and the tertiary nitrogen atom an intramolecular hydrogen bond which can very in strength.
L. Bernardi, W. Barbieri
openaire   +1 more source

Ergoline derivatives: receptor affinity and selectivity

Il Farmaco, 1999
Ergot comprises a group of indole alkaloids which are predominantly found in various species of the ascomycete Claviceps. In pharmacopoeias, the sclerotia of Claviceps purpurea (Fr.) Tulasne parasitizing on rye, Secale cereale L., are designed as ergot or Secale cornutum.
S, Mantegani, E, Brambilla, M, Varasi
openaire   +2 more sources

Nidation Inhibition by Simple Ergoline Derivatives

Journal of Pharmaceutical Sciences, 1975
The ability of four ergoline-type compounds (elymoclavine, its O-benzoate and O-carbamate, and N-methyl-6,7-secoelymoclavine) to inhibit nidation in rats was determined and found to parallel their prolactin-inhibiting activity.
K, Rezábek, J M, Cassady, H G, Floss
openaire   +2 more sources

Ergoline Alkaloids in Tropical Wood Roses

Science, 1965
Extracts of Argyreia nervosa , a tropical wood rose, contain appreciable quantities of ergoline alkaloids tentatively identified as ergine isoergine, and penniclavine together with related substances.
J W, Hylin, D P, Watson
openaire   +2 more sources

1,2-Fused derivatives of ergoline

Collection of Czechoslovak Chemical Communications, 1982
2-Formylergoline derivatives I and II were condensed with methyl isonitrilacetate in the presence of a base. Depending on the nature of this base, the main products of the reaction were either derivatives of pyrimido[1,6-a]ergoline, III and IV, or derivatives of 2-formylamino-3-oxo-3H-pyrrolo[1,2-a]ergoline, V and VI.
Jan Beneš, Jiří Holubek
openaire   +1 more source

2-Acylated derivatives of ergoline

Collection of Czechoslovak Chemical Communications, 1982
Reactions of ergoline derivatives Ia-VIIa with anhydrides of low-molecular-weight aliphatic acids, catalysed by boron trifluoride etherate, gave 2-acylated derivatives Ib-Id, IIb-IId, IIIb-Vb, or 1,2-diacylated derivatives VIb and VIIb. The compound IIb exhibited a hypotensive effect.
Jan Beneš, Jiří Křepelka
openaire   +1 more source

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