Meyners C - Search Results

1

Structure-Based Discovery of a New Selectivity-Enabling Motif for the FK506-Binding Protein 51.

Knaup FH, Meyners C, Sugiarto WO, Wedel S, Springer M, Walz C, Geiger TM, Schmidt M, Sisignano M, Hausch F. Knaup FH, et al. Among authors: meyners c. J Med Chem. 2023 Apr 27;66(8):5965-5980. doi: 10.1021/acs.jmedchem.3c00249. Epub 2023 Apr 14. J Med Chem. 2023. PMID: 37058391

2

Potent and Selective Non-hydroxamate Histone Deacetylase 8 Inhibitors.

Kleinschek A, Meyners C, Digiorgio E, Brancolini C, Meyer-Almes FJ. Kleinschek A, et al. Among authors: meyners c. ChemMedChem. 2016 Dec 6;11(23):2598-2606. doi: 10.1002/cmdc.201600528. Epub 2016 Nov 9. ChemMedChem. 2016. PMID: 27860422

3

Kinetic method for the large-scale analysis of the binding mechanism of histone deacetylase inhibitors.

Meyners C, Baud MG, Fuchter MJ, Meyer-Almes FJ. Meyners C, et al. Anal Biochem. 2014 Sep 1;460:39-46. doi: 10.1016/j.ab.2014.05.014. Epub 2014 Jun 2. Anal Biochem. 2014. PMID: 24882269

4

Features of the transglutaminase-activating metalloprotease from Streptomyces mobaraensis DSM 40847 produced in Escherichia coli.

Juettner NE, Classen M, Colin F, Hoffmann SB, Meyners C, Pfeifer F, Fuchsbauer HL. Juettner NE, et al. Among authors: meyners c. J Biotechnol. 2018 Sep 10;281:115-122. doi: 10.1016/j.jbiotec.2018.07.004. Epub 2018 Jul 4. J Biotechnol. 2018. PMID: 29981445

5

The enzyme activity of histone deacetylase 8 is modulated by a redox-switch.

Jänsch N, Meyners C, Muth M, Kopranovic A, Witt O, Oehme I, Meyer-Almes FJ. Jänsch N, et al. Among authors: meyners c. Redox Biol. 2019 Jan;20:60-67. doi: 10.1016/j.redox.2018.09.013. Epub 2018 Sep 27. Redox Biol. 2019. PMID: 30292946 Free PMC article.

6

The Many Faces of FKBP51.

Hähle A, Merz S, Meyners C, Hausch F. Hähle A, et al. Among authors: meyners c. Biomolecules. 2019 Jan 21;9(1):35. doi: 10.3390/biom9010035. Biomolecules. 2019. PMID: 30669684 Free PMC article. Review.

7

Initial Metabolic Step of a Novel Ethanolamine Utilization Pathway and Its Regulation in Streptomyces coelicolor M145.

Krysenko S, Matthews A, Okoniewski N, Kulik A, Girbas MG, Tsypik O, Meyners CS, Hausch F, Wohlleben W, Bera A. Krysenko S, et al. mBio. 2019 May 21;10(3):e00326-19. doi: 10.1128/mBio.00326-19. mBio. 2019. PMID: 31113893 Free PMC article.

8

FKBP51 and FKBP12.6-Novel and tight interactors of Glomulin.

Hähle A, Geiger TM, Merz S, Meyners C, Tianqi M, Kolos J, Hausch F. Hähle A, et al. Among authors: meyners c. PLoS One. 2019 Sep 6;14(9):e0221926. doi: 10.1371/journal.pone.0221926. eCollection 2019. PLoS One. 2019. PMID: 31490997 Free PMC article.

9

Enantioselective Synthesis of a Tricyclic, sp³ -Rich Diazatetradecanedione: an Amino Acid-Based Natural Product-Like Scaffold.

Bischoff M, Mayer P, Meyners C, Hausch F. Bischoff M, et al. Among authors: meyners c. Chemistry. 2020 Apr 9;26(21):4677-4681. doi: 10.1002/chem.201905144. Epub 2020 Feb 19. Chemistry. 2020. PMID: 31846111 Free PMC article.

10

Structure-Based Design of High-Affinity Macrocyclic FKBP51 Inhibitors.

Bauder M, Meyners C, Purder PL, Merz S, Sugiarto WO, Voll AM, Heymann T, Hausch F. Bauder M, et al. Among authors: meyners c. J Med Chem. 2021 Mar 25;64(6):3320-3349. doi: 10.1021/acs.jmedchem.0c02195. Epub 2021 Mar 5. J Med Chem. 2021. PMID: 33666419

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