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Results: 1-3 |
Results: 3
Conjugated enynes as nonaromatic catechol bioisosteres: Synthesis, bindingexperiments, and computational studies of novel dopamine receptor agonistsrecognizing preferentially the D-3 subtype
Authors: Hubner, H Haubmann, C Utz, W Gmeiner, P
Citation: H. Hubner et al., Conjugated enynes as nonaromatic catechol bioisosteres: Synthesis, bindingexperiments, and computational studies of novel dopamine receptor agonistsrecognizing preferentially the D-3 subtype, J MED CHEM, 43(4), 2000, pp. 756-762
Piperidinylpyrroles: Design, synthesis and binding properties of novel andselective dopamine D4 receptor ligands
Authors: Haubmann, C Hubner, H Gmeiner, P
Citation: C. Haubmann et al., Piperidinylpyrroles: Design, synthesis and binding properties of novel andselective dopamine D4 receptor ligands, BIOORG MED, 9(21), 1999, pp. 3143-3146
2,2-Dicyanovinyl as a nonaromatic aryl bioisostere: Synthesis, binding experiments and SAR studies of highly selective dopamine D4 receptor ligands
Authors: Haubmann, C Hubner, H Gmeiner, P
Citation: C. Haubmann et al., 2,2-Dicyanovinyl as a nonaromatic aryl bioisostere: Synthesis, binding experiments and SAR studies of highly selective dopamine D4 receptor ligands, BIOORG MED, 9(14), 1999, pp. 1969-1972
Risultati: 1-3 |