nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Affinity and kinetics study of anthranilic acids as HCA2 receptor agonists
|
van Veldhoven, Jacobus P.D. |
|
2015 |
23 |
14 |
p. 4013-4025 13 p. |
artikel |
2 |
Cell-based and virtual fragment screening for adrenergic α2C receptor agonists
|
Szőllősi, Edit |
|
2015 |
23 |
14 |
p. 3991-3999 9 p. |
artikel |
3 |
Dimeric carbamoylguanidine-type histamine H2 receptor ligands: A new class of potent and selective agonists
|
Kagermeier, Nicole |
|
2015 |
23 |
14 |
p. 3957-3969 13 p. |
artikel |
4 |
Editorial board
|
|
|
2015 |
23 |
14 |
p. IFC- 1 p. |
artikel |
5 |
Fluoro-substituted phenylazocarboxamides: Dopaminergic behavior and N-arylating properties for irreversible binding
|
Bartuschat, Amelie L. |
|
2015 |
23 |
14 |
p. 3938-3947 10 p. |
artikel |
6 |
GPCR crystal structures: Medicinal chemistry in the pocket
|
Shonberg, Jeremy |
|
2015 |
23 |
14 |
p. 3880-3906 27 p. |
artikel |
7 |
Graphical contents list
|
|
|
2015 |
23 |
14 |
p. 3873-3878 6 p. |
artikel |
8 |
High metabolic in vivo stability and bioavailability of a palmitoylated ghrelin receptor ligand assessed by mass spectrometry
|
Kostelnik, Katja B. |
|
2015 |
23 |
14 |
p. 3925-3932 8 p. |
artikel |
9 |
Improved radiosynthesis and preliminary in vivo evaluation of a 18F-labeled glycopeptide–peptoid hybrid for PET imaging of neurotensin receptor 2
|
Maschauer, Simone |
|
2015 |
23 |
14 |
p. 4026-4033 8 p. |
artikel |
10 |
Ligand selectivity of a synthetic CXCR4 mimetic peptide
|
Groß, Andrea |
|
2015 |
23 |
14 |
p. 4050-4055 6 p. |
artikel |
11 |
Molecular modeling of the human P2Y14 receptor: A template for structure-based design of selective agonist ligands
|
Trujillo, Kevin |
|
2015 |
23 |
14 |
p. 4056-4064 9 p. |
artikel |
12 |
M2 Subtype preferring dibenzodiazepinone-type muscarinic receptor ligands: Effect of chemical homo-dimerization on orthosteric (and allosteric?) binding
|
Keller, Max |
|
2015 |
23 |
14 |
p. 3970-3990 21 p. |
artikel |
13 |
Non-peptide ligand binding to the formyl peptide receptor FPR2—A comparison to peptide ligand binding modes
|
Stepniewski, Tomasz M. |
|
2015 |
23 |
14 |
p. 4072-4081 10 p. |
artikel |
14 |
Novel 3-(1H-indol-3-yl)-2-[3-(4-methoxyphenyl)ureido]propanamides as selective agonists of human formyl-peptide receptor 2
|
Lacivita, Enza |
|
2015 |
23 |
14 |
p. 3913-3924 12 p. |
artikel |
15 |
Potency enhancement of the κ-opioid receptor antagonist probe ML140 through sulfonamide constraint utilizing a tetrahydroisoquinoline motif
|
Frankowski, Kevin J. |
|
2015 |
23 |
14 |
p. 3948-3956 9 p. |
artikel |
16 |
Promiscuity and selectivity of bitter molecules and their receptors
|
Di Pizio, Antonella |
|
2015 |
23 |
14 |
p. 4082-4091 10 p. |
artikel |
17 |
Selective GPCR ligands
|
Gmeiner, Peter |
|
2015 |
23 |
14 |
p. 3879- 1 p. |
artikel |
18 |
Structure versus function—The impact of computational methods on the discovery of specific GPCR–ligands
|
Bermudez, Marcel |
|
2015 |
23 |
14 |
p. 3907-3912 6 p. |
artikel |
19 |
Synthesis and biological evaluation of spirocyclic antagonists of CCR2 (chemokine CC receptor subtype 2)
|
Strunz, Ann Kathrin |
|
2015 |
23 |
14 |
p. 4034-4049 16 p. |
artikel |
20 |
Synthesis and pharmacological evaluation of N-benzyl substituted 4-bromo-2,5-dimethoxyphenethylamines as 5-HT2A/2C partial agonists
|
Hansen, Martin |
|
2015 |
23 |
14 |
p. 3933-3937 5 p. |
artikel |
21 |
Understanding allosteric interactions in G protein-coupled receptors using Supervised Molecular Dynamics: A prototype study analysing the human A3 adenosine receptor positive allosteric modulator LUF6000
|
Deganutti, Giuseppe |
|
2015 |
23 |
14 |
p. 4065-4071 7 p. |
artikel |
22 |
Using click chemistry toward novel 1,2,3-triazole-linked dopamine D3 receptor ligands
|
Keck, Thomas M. |
|
2015 |
23 |
14 |
p. 4000-4012 13 p. |
artikel |