Döring E - Search Results

1

Ro-Vibrational Spectrum of Vanadium Monoxide (VO) at 10 μm.

Döring E, Blum L, Breier AA, Giesen TF, Fuchs GW. Döring E, et al. J Phys Chem A. 2024 Dec 16. doi: 10.1021/acs.jpca.4c05996. Online ahead of print. J Phys Chem A. 2024. PMID: 39680865

2

Ro-vibrational Spectrum of Linear Dialuminum Monoxide (Al₂O) at 10 μm.

Witsch D, Döring E, Breier AA, Gauss J, Giesen TF, Fuchs GW. Witsch D, et al. Among authors: doring e. J Phys Chem A. 2023 May 4;127(17):3824-3831. doi: 10.1021/acs.jpca.3c00989. Epub 2023 Apr 25. J Phys Chem A. 2023. PMID: 37097756

3

High-resolution infrared spectra and rovibrational analysis of the ν₁₂ band of propylene oxide.

Vávra K, Döring E, Jakob J, Peterß F, Kaufmann M, Stahl P, Giesen TF, Fuchs GW. Vávra K, et al. Among authors: doring e. Phys Chem Chem Phys. 2024 Sep 18;26(36):23886-23892. doi: 10.1039/d4cp02943g. Phys Chem Chem Phys. 2024. PMID: 39233485

4

Pyridinylimidazoles as dual glycogen synthase kinase 3β/p38α mitogen-activated protein kinase inhibitors.

Heider F, Ansideri F, Tesch R, Pantsar T, Haun U, Döring E, Kudolo M, Poso A, Albrecht W, Laufer SA, Koch P. Heider F, et al. Among authors: doring e. Eur J Med Chem. 2019 Aug 1;175:309-329. doi: 10.1016/j.ejmech.2019.04.035. Epub 2019 Apr 24. Eur J Med Chem. 2019. PMID: 31096153

5

Natural chromones as potential anti-inflammatory agents: Pharmacological properties and related mechanisms.

Opretzka LCF, Espírito-Santo RFD, Nascimento OA, Abreu LS, Alves IM, Döring E, Soares MBP, Velozo EDS, Laufer SA, Villarreal CF. Opretzka LCF, et al. Among authors: doring e. Int Immunopharmacol. 2019 Jul;72:31-39. doi: 10.1016/j.intimp.2019.03.044. Epub 2019 Apr 5. Int Immunopharmacol. 2019. PMID: 30959369 Free article.

6

Development, Optimization, and Structure-Activity Relationships of Covalent-Reversible JAK3 Inhibitors Based on a Tricyclic Imidazo[5,4- d]pyrrolo[2,3- b]pyridine Scaffold.

Forster M, Chaikuad A, Dimitrov T, Döring E, Holstein J, Berger BT, Gehringer M, Ghoreschi K, Müller S, Knapp S, Laufer SA. Forster M, et al. Among authors: doring e. J Med Chem. 2018 Jun 28;61(12):5350-5366. doi: 10.1021/acs.jmedchem.8b00571. Epub 2018 Jun 13. J Med Chem. 2018. PMID: 29852068

7

From 2-Alkylsulfanylimidazoles to 2-Alkylimidazoles: An Approach towards Metabolically More Stable p38α MAP Kinase Inhibitors.

Heider F, Haun U, Döring E, Kudolo M, Sessler C, Albrecht W, Laufer S, Koch P. Heider F, et al. Among authors: doring e. Molecules. 2017 Oct 14;22(10):1729. doi: 10.3390/molecules22101729. Molecules. 2017. PMID: 29036906 Free PMC article.

8

Design, Synthesis, and Biological Evaluation of Novel Type I¹/₂ p38α MAP Kinase Inhibitors with Excellent Selectivity, High Potency, and Prolonged Target Residence Time by Interfering with the R-Spine.

Walter NM, Wentsch HK, Bührmann M, Bauer SM, Döring E, Mayer-Wrangowski S, Sievers-Engler A, Willemsen-Seegers N, Zaman G, Buijsman R, Lämmerhofer M, Rauh D, Laufer SA. Walter NM, et al. Among authors: doring e. J Med Chem. 2017 Oct 12;60(19):8027-8054. doi: 10.1021/acs.jmedchem.7b00745. Epub 2017 Sep 7. J Med Chem. 2017. PMID: 28834431

9

Trisubstituted Pyridinylimidazoles as Potent Inhibitors of the Clinically Resistant L858R/T790M/C797S EGFR Mutant: Targeting of Both Hydrophobic Regions and the Phosphate Binding Site.

Günther M, Lategahn J, Juchum M, Döring E, Keul M, Engel J, Tumbrink HL, Rauh D, Laufer S. Günther M, et al. Among authors: doring e. J Med Chem. 2017 Jul 13;60(13):5613-5637. doi: 10.1021/acs.jmedchem.7b00316. Epub 2017 Jun 21. J Med Chem. 2017. PMID: 28603991

10

Trisubstituted Imidazoles with a Rigidized Hinge Binding Motif Act As Single Digit nM Inhibitors of Clinically Relevant EGFR L858R/T790M and L858R/T790M/C797S Mutants: An Example of Target Hopping.

Juchum M, Günther M, Döring E, Sievers-Engler A, Lämmerhofer M, Laufer S. Juchum M, et al. Among authors: doring e. J Med Chem. 2017 Jun 8;60(11):4636-4656. doi: 10.1021/acs.jmedchem.7b00178. Epub 2017 May 23. J Med Chem. 2017. PMID: 28482151

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