Götz MG - Search Results

1

Aza-peptidyl Michael acceptors. A new class of potent and selective inhibitors of asparaginyl endopeptidases (legumains) from evolutionarily diverse pathogens.

Götz MG, James KE, Hansell E, Dvorák J, Seshaadri A, Sojka D, Kopácek P, McKerrow JH, Caffrey CR, Powers JC. Götz MG, et al. J Med Chem. 2008 May 8;51(9):2816-32. doi: 10.1021/jm701311r. Epub 2008 Apr 17. J Med Chem. 2008. PMID: 18416543

2

Aza-peptide epoxides: potent and selective inhibitors of Schistosoma mansoni and pig kidney legumains (asparaginyl endopeptidases).

James KE, Götz MG, Caffrey CR, Hansell E, Carter W, Barrett AJ, McKerrow JH, Powers JC. James KE, et al. Among authors: gotz mg. Biol Chem. 2003 Dec;384(12):1613-8. doi: 10.1515/BC.2003.179. Biol Chem. 2003. PMID: 14719804

3

Aza-peptide Michael acceptors: a new class of inhibitors specific for caspases and other clan CD cysteine proteases.

Ekici OD, Götz MG, James KE, Li ZZ, Rukamp BJ, Asgian JL, Caffrey CR, Hansell E, Dvorák J, McKerrow JH, Potempa J, Travis J, Mikolajczyk J, Salvesen GS, Powers JC. Ekici OD, et al. Among authors: gotz mg. J Med Chem. 2004 Apr 8;47(8):1889-92. doi: 10.1021/jm049938j. J Med Chem. 2004. PMID: 15055989

4

Peptidyl allyl sulfones: a new class of inhibitors for clan CA cysteine proteases.

Götz MG, Caffrey CR, Hansell E, McKerrow JH, Powers JC. Götz MG, et al. Bioorg Med Chem. 2004 Oct 1;12(19):5203-11. doi: 10.1016/j.bmc.2004.07.016. Bioorg Med Chem. 2004. PMID: 15351403

5

Design and evaluation of inhibitors for dipeptidyl peptidase I (Cathepsin C).

Kam CM, Götz MG, Koot G, McGuire M, Thiele D, Hudig D, Powers JC. Kam CM, et al. Among authors: gotz mg. Arch Biochem Biophys. 2004 Jul 15;427(2):123-34. doi: 10.1016/j.abb.2004.04.011. Arch Biochem Biophys. 2004. PMID: 15196986

6

Optimization of peptidyl allyl sulfones as clan CA cysteine protease inhibitors.

Fennell BD, Warren JM, Chung KK, Main HL, Arend AB, Tochowicz A, Götz MG. Fennell BD, et al. Among authors: gotz mg. J Enzyme Inhib Med Chem. 2013 Jun;28(3):468-78. doi: 10.3109/14756366.2011.651466. Epub 2012 Mar 1. J Enzyme Inhib Med Chem. 2013. PMID: 22380780 Free article.

7

Synthesis and Evaluation of Macrocyclic Peptide Aldehydes as Potent and Selective Inhibitors of the 20S Proteasome.

Wilson DL, Meininger I, Strater Z, Steiner S, Tomlin F, Wu J, Jamali H, Krappmann D, Götz MG. Wilson DL, et al. Among authors: gotz mg. ACS Med Chem Lett. 2016 Jan 15;7(3):250-5. doi: 10.1021/acsmedchemlett.5b00401. eCollection 2016 Mar 10. ACS Med Chem Lett. 2016. PMID: 26985310 Free PMC article.

8

Luteinizing hormone-releasing hormone and analogs. Synthesis and biological activity.

Immer H, Nelson VR, Revesz C, Sestanj K, Götz M. Immer H, et al. J Med Chem. 1974 Oct;17(10):1060-5. doi: 10.1021/jm00256a007. J Med Chem. 1974. PMID: 4608382 No abstract available.

9

TMC-95-based inhibitor design provides evidence for the catalytic versatility of the proteasome.

Groll M, Götz M, Kaiser M, Weyher E, Moroder L. Groll M, et al. Chem Biol. 2006 Jun;13(6):607-14. doi: 10.1016/j.chembiol.2006.04.005. Chem Biol. 2006. PMID: 16793518

10

Visible-light photocatalyzed cross-linking of diacetylene ligands by quantum dots to improve their aqueous colloidal stability.

Götz MG, Takeuchi H, Goldfogel MJ, Warren JM, Fennell BD, Heyes CD. Götz MG, et al. J Phys Chem B. 2014 Dec 11;118(49):14103-9. doi: 10.1021/jp505340c. Epub 2014 Jul 28. J Phys Chem B. 2014. PMID: 25036275 Free PMC article.

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