Wünsch B - Search Results

1

Design and Synthesis of Enantiomerically Pure Decahydroquinoxalines as Potent and Selective κ-Opioid Receptor Agonists with Anti-Inflammatory Activity in Vivo.

Soeberdt M, Molenveld P, Storcken RP, Bouzanne des Mazery R, Sterk GJ, Autar R, Bolster MG, Wagner C, Aerts SN, van Holst FR, Wegert A, Tangherlini G, Frehland B, Schepmann D, Metze D, Lotts T, Knie U, Lin KY, Huang TY, Lai CC, Ständer S, Wünsch B, Abels C. Soeberdt M, et al. Among authors: wunsch b. J Med Chem. 2017 Mar 23;60(6):2526-2551. doi: 10.1021/acs.jmedchem.6b01868. Epub 2017 Mar 13. J Med Chem. 2017. PMID: 28218838

2

Synthesis and stereoselective kappa-receptor binding of methylated analogues of GR-89.696.

Röhr C, Soukara S, Wünsch B. Röhr C, et al. Among authors: wunsch b. Eur J Med Chem. 2001 Feb;36(2):211-4. doi: 10.1016/s0223-5234(00)01208-3. Eur J Med Chem. 2001. PMID: 11311752

3

Methylated analogues of methyl (R)-4-(3,4-dichlorophenylacetyl)- 3-(pyrrolidin-1-ylmethyl)piperazine-1-carboxylate (GR-89,696) as highly potent kappa-receptor agonists: stereoselective synthesis, opioid-receptor affinity, receptor selectivity, and functional studies.

Soukara S, Maier CA, Predoiu U, Ehret A, Jackisch R, Wünsch B. Soukara S, et al. Among authors: wunsch b. J Med Chem. 2001 Aug 16;44(17):2814-26. doi: 10.1021/jm0108395. J Med Chem. 2001. PMID: 11495592

4

Novel spiropiperidines as highly potent and subtype selective sigma-receptor ligands. Part 1.

Maier CA, Wünsch B. Maier CA, et al. Among authors: wunsch b. J Med Chem. 2002 Jan 17;45(2):438-48. doi: 10.1021/jm010992z. J Med Chem. 2002. PMID: 11784148

5

Conformationally constrained ethylenediamines: synthesis and receptor binding of 6,8-diazabicyclo[3.2.2]nonanes.

Weigl M, Bedürftig S, Maier CA, Wünsch B. Weigl M, et al. Among authors: wunsch b. Bioorg Med Chem. 2002 Jul;10(7):2245-57. doi: 10.1016/s0968-0896(02)00043-3. Bioorg Med Chem. 2002. PMID: 11983522

6

Novel sigma receptor ligands. Part 2. SAR of spiro[[2]benzopyran-1,4'-piperidines] and spiro[[2]benzofuran-1,4'-piperidines] with carbon substituents in position 3.

Maier CA, Wünsch B. Maier CA, et al. Among authors: wunsch b. J Med Chem. 2002 Oct 24;45(22):4923-30. doi: 10.1021/jm020889p. J Med Chem. 2002. PMID: 12383018

7

Synthesis and structure/NMDA receptor affinity relationships of 1-substituted tetrahydro-3-benzazepines.

Krull O, Wünsch B. Krull O, et al. Among authors: wunsch b. Bioorg Med Chem. 2004 Mar 15;12(6):1439-51. doi: 10.1016/j.bmc.2003.12.036. Bioorg Med Chem. 2004. PMID: 15018917

8

Structure-affinity relationship studies of non-competitive NMDA receptor antagonists derived from dexoxadrol and etoxadrol.

Aepkers M, Wünsch B. Aepkers M, et al. Among authors: wunsch b. Bioorg Med Chem. 2005 Dec 15;13(24):6836-49. doi: 10.1016/j.bmc.2005.07.030. Epub 2005 Sep 19. Bioorg Med Chem. 2005. PMID: 16169732

9

Synthesis and receptor binding studies of 3-substituted piperazine derivatives.

Bedürftig S, Wünsch B. Bedürftig S, et al. Among authors: wunsch b. Eur J Med Chem. 2006 Mar;41(3):387-96. doi: 10.1016/j.ejmech.2005.09.004. Epub 2006 Jan 30. Eur J Med Chem. 2006. PMID: 16446011

10

Relationships between the structure of dexoxadrol and etoxadrol analogues and their NMDA receptor affinity.

Sax M, Wünsch B. Sax M, et al. Among authors: wunsch b. Curr Top Med Chem. 2006;6(7):723-32. doi: 10.2174/156802606776894483. Curr Top Med Chem. 2006. PMID: 16719812 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

321 results

Search Page