M. Seiler

发表

CY 208-243: a unique combination of atypical opioid antinociception and D1 dopaminomimetic properties.

R. W. Foote, B. Gähwiler, A. Enz, 1988, Life sciences.

5‐HT1‐like receptors mediate 5‐hydroxytryptamine‐induced contraction of guinea‐pig isolated iliac artery

D. Hoyer, P. Schoeffter, A. Stoll, 1991, British journal of pharmacology.

Differential inverse agonist efficacies of SB-258719, SB-258741 and SB-269970 at human recombinant serotonin 5-HT7 receptors.

Philippe Schoeffter, E. Loetscher, P. Schoeffter, 2004, European journal of pharmacology.

SDZ 216-525, a selective and potent 5-HT1A receptor antagonist.

J. Fozard, P. Schoeffter, A. Stoll, 1993, European journal of pharmacology.

Structure-activity relationships of dopaminergic 5-hydroxy-2-aminotetralin derivatives with functionalized N-alkyl substituents.

A. Jaton, M. Seiler, J. Vigouret, 1986, Journal of medicinal chemistry.

Characterization of dopamine receptor subtypes by comparative structure-activity relationships: dopaminomimetic activities and solid state conformation of monohydroxy-1,2,3,4,4a,5,10,10a-octahydrobenz[g]quinolines and its implications for a rotamer-based dopamine receptor model.

M. Walkinshaw, R. Markstein, J. Boelsterli, 1989, Molecular pharmacology.

trans-hexahydroindolo[4,3-ab]phenanthridines ("benzergolines"), the first structural class of potent and selective dopamine D1 receptor agonists lacking a catechol group.

R. Markstein, M. Seiler, H. Wüthrich, 1991, Journal of medicinal chemistry.

trans-Hexahydroindolo(4,3-ab)phenanthridines (“Benzergolines”), the First Structural Class of Potent and Selective Dopamine D1 Receptor Agonists Lacking a Catechol Group.

R. Markstein, H. Wuethrich, M. Seiler, 2010 .

Structure activity relationship and therapeutic uses of dopaminergic ergots

A. Jaton, U. Briner, R. Markstein, 1992, Neurochemistry International.

Identification and biological characterization of 6-aryl-7-isopropylquinazolinones as novel TRPV1 antagonists that are effective in models of chronic pain.

P. McIntyre, S. Bevan, A. Dyson, 2006, Journal of medicinal chemistry.