Löber S, Hübner H, Gmeiner P (1999)
Publication Type: Journal article
Publication year: 1999
Publisher: Elsevier
Book Volume: 9
Pages Range: 97-102
DOI: 10.1016/S0960-894X(98)00692-1
Piperazinylmethyl substituted pyrazolo[1,5-a]pyridines and related heterocycles were synthesized and found to recognize selectively the dopamine D4 receptor. For the most potent derivative 10d a Ki value of 2.0 nM was observed. SAR studies including the comparison of molecular isopotential surfaces were performed.
APA:
Löber, S., Hübner, H., & Gmeiner, P. (1999). Azaindole Derivatives with High Affinity for the Dopamine D4 Receptor: Synthesis, Ligand Binding Studies and Comparison of Molecular Electrostatic Potential Maps. Bioorganic & Medicinal Chemistry Letters, 9, 97-102. https://doi.org/10.1016/S0960-894X(98)00692-1
MLA:
Löber, Stefan, Harald Hübner, and Peter Gmeiner. "Azaindole Derivatives with High Affinity for the Dopamine D4 Receptor: Synthesis, Ligand Binding Studies and Comparison of Molecular Electrostatic Potential Maps." Bioorganic & Medicinal Chemistry Letters 9 (1999): 97-102.
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