Authors:
Windhorst, AD
Timmerman, H
Worthington, EA
Bijloo, GJ
Nederkoorn, PHJ
Menge, WMPB
Leurs, R
Herscheid, JDM
Citation: Ad. Windhorst et al., Characterization of the binding site of the histamine H-3 receptor. 2. Synthesis, in vitro pharmacology, and QSAR of a series of monosubstituted benzyl analogues of thioperamide, J MED CHEM, 43(9), 2000, pp. 1754-1761
Authors:
Windhorst, AD
Timmerman, H
Klok, RP
Custers, FGJ
Menge, WMPB
Leurs, R
Stark, H
Schunack, W
Gielen, EGJ
van Kroonenburgh, MJPG
Herscheid, JDM
Citation: Ad. Windhorst et al., Radiosynthesis and biodistribution of I-123-labeled antagonists of the histamine H-3 receptor as potential SPECT ligands, NUCL MED BI, 26(6), 1999, pp. 651-659
Authors:
Windhorst, AD
Timmerman, H
Klok, RP
Menge, WMPB
Leurs, R
Herscheid, JDM
Citation: Ad. Windhorst et al., Evaluation of [F-18]VUF 5000 as a potential PET ligand for brain imaging of the histamine H-3 receptor, BIO MED CH, 7(9), 1999, pp. 1761-1767
Authors:
Windhorst, AD
Timmerman, H
Menge, WMPB
Leurs, R
Herscheid, JDM
Citation: Ad. Windhorst et al., Synthesis, in vitro pharmacology and radiosynthesis of N-(cis-4-fluoromethylcyclohexyl)-4-(1(H)-imidazol-4-yl)piperidine-1-thiocarbonamide (VUF 5000), a potential pet ligand for the histamine H-3 receptor., J LABEL C R, 42(3), 1999, pp. 293-307