Results 101 to 110 of about 1,990 (193)

Females in Psychedelic Research: A Perspective for Advancing Research and Practice. [PDF]

ACS Pharmacol Transl Sci
Cohen ZZ, Blest-Hopley G.
europepmc   +1 more source

Five cases of tremorgenic mycotoxicosis in dogs - clinical aspects and analytical methods. [PDF]

Vet Res Commun
Hart L, Rehagel C, Kuhn M, Taube A, Jozefowitz L, Hassdenteufel E, Cramer B, Akineden Ö, Usleber E.   +8 more
europepmc   +1 more source

Serotonin 5-HT_2C Receptor Signaling Analysis Reveals Psychedelic Biased Agonism. [PDF]

ACS Chem Neurosci
Bonniwell EM, Alabdali R, Hennessey JJ, McKee JL, Cavalco NG, Lammers JC, Moore EJ, Franchini L, Orlandi C, McCorvy JD.   +9 more
europepmc   +1 more source

Reconsideration of Surgical Indication for Prolactin-producing Pituitary Tumor Focusing on Visual Impairment. [PDF]

Neurol Med Chir (Tokyo)
Amano K, Oda Y, Seki Y, Yamashita K, Bokuda K, Ichihara A, Kawamata T.   +6 more
europepmc   +1 more source

Psilocybin as Transformative Fast-Acting Antidepressant: Pharmacological Properties and Molecular Mechanisms. [PDF]

Fundam Clin Pharmacol
Adebo M, Bonnet M, Laouej O, Defaix C, McGowan JC, Butlen-Ducuing F, David DJ, Poupon E, Tritschler L, Gardier AM.   +9 more
europepmc   +1 more source

Biased Signaling in Psychedelic Action. [PDF]

Annu Rev Pharmacol Toxicol
Wacker D, McCorvy JD.
europepmc   +1 more source

Inhibition of Prolactin Secretion by Ergolines.

Endocrinology, 1974
Peptide-containing ergot alkaloids and synthetic ergoline derivatives were administered to reserpine-treated male rats in order to evaluate their prolactin-inhibiting properties. Each compound was administered ip at a standard 50 ¼g/kg dose. The 9,10-dihydrogenated ergots, dihydroergocornine, and dihydroergocryptine were able to inhibit prolactin to ...
C J Shaar, Edmund C Kornfeld, J A Clemens   +2 more
exaly   +5 more sources

On the Alleged Electrochemical Methoxylation of Ergolines

Tetrahedron Letters, 1983
The products obtained by controlled potential electrolysis of ergolines (1) in 0.5N KOH-MeOH previously described as 2-methoxy derivatives (2) are actually the 1-hydroxy methyl ergolines (3)
Giovanni Palmisano, Bruno Danieli
exaly   +4 more sources

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Ergolines as Selective 5-HT1 Agonists

Journal of Medicinal Chemistry, 1988
The synthesis and serotonin receptor subtype affinity of a series of ergolines are described. High selectivity for the 5-HT1 subtype was found with a number of 8-substituted (3 beta, 5 beta)-9,10-didehydro-6-methylergolines. The more potent and selective of these compounds increased the concentration of serotonin and decreased the concentration of 5 ...
John S Ward, Harold D Snoddy, Ray W Fuller   +2 more
exaly   +4 more sources

Regiocontrolled Electrochemical Cyanation of Ergolines

Tetrahedron Letters, 1983
K. Seifert, S. Haertling, S. Johne
exaly   +3 more sources