lysergic acid has been researched along with 9,10-dihydrolysergol in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 2 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (25.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Eich, E; Pertz, H | 1 |
Johne, S; Seifert, K | 1 |
Eich, E; Milhahn, H; Pertz, HH | 1 |
Bragg, PE; Maust, MD; Panaccione, DG | 1 |
4 other study(ies) available for lysergic acid and 9,10-dihydrolysergol
Article | Year |
---|---|
O-acylated lysergol and dihydrolysergol-I derivatives as competitive antagonists of 5-HT at 5-HT2 receptors of rat tail artery. Allosteric modulation instead of pseudoirreversible inhibition.
Topics: Animals; Binding, Competitive; Ergolines; In Vitro Techniques; Lysergic Acid; Male; Methysergide; Muscle Contraction; Muscle, Smooth, Vascular; Phenylephrine; Rats; Rats, Inbred Strains; Receptors, Adrenergic, alpha; Regional Blood Flow; Serotonin Antagonists; Tail | 1992 |
[Synthesis of glycosides and sugar orthoesters of 9,10-dihydrolysergol].
Topics: Animals; Chemical Phenomena; Chemistry; Ergolines; Lysergic Acid; Magnetic Resonance Spectroscopy; Prolactin; Rats | 1984 |
Cycloalkanecarboxylic esters derived from lysergol, dihydrolysergol-I, and elymoclavine as partial agonists and antagonists at rat 5-HT2A receptors: pharmacological evidence that the indolo[4,3-fg]quinoline system of the ergolines is responsible for high
Topics: Animals; Aorta, Thoracic; Arteries; Ergolines; Female; Guinea Pigs; Iliac Artery; In Vitro Techniques; Lysergic Acid; Male; Muscle Contraction; Muscle, Smooth, Vascular; Rats; Rats, Wistar; Receptor, Serotonin, 5-HT1B; Receptor, Serotonin, 5-HT2A; Receptors, Adrenergic, alpha-1; Receptors, Serotonin; Serotonin Antagonists; Serotonin Receptor Agonists; Tail | 1999 |
Ergot Alkaloid Biosynthesis in the Maize (Zea mays) Ergot Fungus Claviceps gigantea.
Topics: Chromatography, High Pressure Liquid; Claviceps; Ergot Alkaloids; Gene Expression; Lysergic Acid; Mass Spectrometry; Mixed Function Oxygenases; Mutation; Secondary Metabolism; Transformation, Genetic; Zea mays | 2017 |