Henk Timmerman
Affiliations: | 1979-2002 | Pharmacochemistry | Vrije Universiteit Amsterdam, Amsterdam, Netherlands |
Website:
https://chg.kncv.nl/geschiedenis/biografieen/t/timmerman%2C-h.Google:
"Henk Timmerman"Mean distance: 13.48 | S | N | B | C | P |
Parents
Sign in to add mentorWybe Th. Nauta | grad student | 1967 | Free University of Amsterdam | |
(2-alkyl-1-[ortho-alkyl-phenyl] cyclohexanols, synthesis, conformation and some pharmacological investigations) |
Children
Sign in to add traineeRob Leurs | grad student | Free University of Amsterdam | |
Ad P. IJzerman | grad student | 1985 | VU Amsterdam |
Martine Joyce Smit | grad student | 1995 | VU Amsterdam |
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Publications
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Kooistra AJ, de Graaf C, Timmerman H. (2014) The receptor concept in 3D: from hypothesis and metaphor to GPCR-ligand structures. Neurochemical Research. 39: 1850-61 |
Paquay JB, Bolscher MT, Voss HP, et al. (2012) Difference in the inhibition of nitric oxide synthase and cytochrome P-450 by some H(2)-antagonists. Toxicology in Vitro : An International Journal Published in Association With Bibra. 11: 775-8 |
Malan SF, van Marle A, Menge WM, et al. (2012) Corrigendum to “Fluorescent ligands for the histamine H2 receptor: Synthesis and preliminary characterization” [Bioorg. Med. Chem. 12 (2004) 6495–6503 Bioorganic & Medicinal Chemistry. 20: 6003 |
Wijtmans M, Denonne F, Célanire S, et al. (2010) Histamine H3 receptor ligands with a 3-cyclobutoxy motif: A novel and versatile constraint of the classical 3-propoxy linker Medchemcomm. 1: 39-44 |
Timmerman H, van der Goot H. (2010) Histamine receptors and their ligands: Mechanisms and applications Encyclopedia of Neuroscience. 1149-1166 |
van Muijlwijk-Koezen JE, Timmerman H, van der Sluis RP, et al. (2010) ChemInform Abstract: Synthesis and Use of FSCPX, an Irreversible Adenosine A1 Antagonist, as a “Receptor Knock-Down” Tool. Cheminform. 32: no-no |
Walczynski K, Guryn R, Zuiderveld OP, et al. (2010) ChemInform Abstract: Non-imidazole Histamine H3 Ligands. Part 1. Synthesis of 2-(1-Piperazinyl)- and 2-(Hexahydro-1H-1,4-diazepin-1-yl)benzothiazole Derivatives as H3-Antagonists with H1 Blocking Activities. Cheminform. 31: no-no |
Walczynski K, Timmerman H, Zuiderveld OP, et al. (2010) ChemInform Abstract: Histamine H1 Receptor Ligands. Part 1. Novel Thiazol-4-ylethanamine Derivatives: Synthesis and in vitro Pharmacology. Cheminform. 30: no-no |
Menge WMPB, Timmerman H. (2010) ChemInform Abstract: Substituted Imidazoles: The Key to Histaminergic Receptors Cheminform. 30: no-no |
ZWAAGSTRA ME, KORTHOUWER REM, TIMMERMAN H, et al. (2010) ChemInform Abstract: Synthesis of 3- and 5′-Substituted Flavone-8-carboxylic Acids as “Three-Armed” Leukotriene CysLT1 Receptor Antagonists. Cheminform. 29: no-no |