Results 131 to 140 of about 1,343 (193)

Microdosing psychedelics and the risk of cardiac fibrosis and valvulopathy: Comparison to known cardiotoxins. [PDF]

J Psychopharmacol
Rouaud A, Calder AE, Hasler G.
europepmc   +1 more source

Chanoclavine synthase operates by an NADPH-independent superoxide mechanism. [PDF]

Nature
Chen CC, Yu ZP, Liu Z, Yao Y, Hagedoorn PL, Schmitz RA, Yang L, Yu L, Liu A, Sheng X, Su H, Ma Y, Wang T, Huang JW, Zhang L, Yan J, Bao J, Cui C, Li X, Shen P, Zhang W, Min J, Wang CY, Guo RT, Gao SS.   +24 more
europepmc   +1 more source

Molecular Mechanisms of Nicergoline from Ergot Fungus in Blocking Human 5-HT3A Receptor. [PDF]

J Microbiol Biotechnol
Pyeon M, Moon M, Yun J, Yang J, Yeom HD, Lee G, Lee JH.   +6 more
europepmc   +1 more source

Uncovering the unique characteristics of different groups of 5-HT_5AR ligands with reference to their interaction with the target protein. [PDF]

Pharmacol Rep
Kordylewski SK, Bugno R, Bojarski AJ, Podlewska S.   +3 more
europepmc   +1 more source

Sistemi per il rimescolamento elettromagnetico di compositi metallici allo stato fuso [PDF]

core  

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   +3 more sources

Ergoline derivatives—XIV

Tetrahedron, 1974
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.
L. Bernardi, E. Gandini, A. Temperilli
openaire   +3 more sources

Ergoline derivatives—IX

Tetrahedron, 1969
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.
Temperilli A, L. Bernardi, W. Barbieri, G. Bosisio   +3 more
openaire   +4 more sources

Studies on the metabolism of ergoline derivatives

Biochemical Pharmacology, 1972
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 ...
A. Minghetti, V. Nicolella, J. Grafnetterova, A.G. Glässer, Federico Arcamone   +4 more
openaire   +4 more sources