Jung M - Search Results

1

Structure-Reactivity Relationships on Substrates and Inhibitors of the Lysine Deacylase Sirtuin 2 from Schistosoma mansoni (SmSirt2).

Monaldi D, Rotili D, Lancelot J, Marek M, Wössner N, Lucidi A, Tomaselli D, Ramos-Morales E, Romier C, Pierce RJ, Mai A, Jung M. Monaldi D, et al. Among authors: jung m. J Med Chem. 2019 Oct 10;62(19):8733-8759. doi: 10.1021/acs.jmedchem.9b00638. Epub 2019 Sep 20. J Med Chem. 2019. PMID: 31496251

2

Structure-activity relationships on phenylalanine-containing inhibitors of histone deacetylase: in vitro enzyme inhibition, induction of differentiation, and inhibition of proliferation in Friend leukemic cells.

Wittich S, Scherf H, Xie C, Brosch G, Loidl P, Gerhäuser C, Jung M. Wittich S, et al. Among authors: jung m. J Med Chem. 2002 Jul 18;45(15):3296-309. doi: 10.1021/jm0208119. J Med Chem. 2002. PMID: 12109913

3

Subtype selective substrates for histone deacetylases.

Heltweg B, Dequiedt F, Marshall BL, Brauch C, Yoshida M, Nishino N, Verdin E, Jung M. Heltweg B, et al. Among authors: jung m. J Med Chem. 2004 Oct 7;47(21):5235-43. doi: 10.1021/jm0497592. J Med Chem. 2004. PMID: 15456267 Free article.

4

Adenosine mimetics as inhibitors of NAD+-dependent histone deacetylases, from kinase to sirtuin inhibition.

Trapp J, Jochum A, Meier R, Saunders L, Marshall B, Kunick C, Verdin E, Goekjian P, Sippl W, Jung M. Trapp J, et al. Among authors: jung m. J Med Chem. 2006 Dec 14;49(25):7307-16. doi: 10.1021/jm060118b. J Med Chem. 2006. PMID: 17149860

5

Target-based approach to inhibitors of histone arginine methyltransferases.

Spannhoff A, Heinke R, Bauer I, Trojer P, Metzger E, Gust R, Schüle R, Brosch G, Sippl W, Jung M. Spannhoff A, et al. Among authors: jung m. J Med Chem. 2007 May 17;50(10):2319-25. doi: 10.1021/jm061250e. Epub 2007 Apr 14. J Med Chem. 2007. PMID: 17432842

6

Phenylalanine-containing hydroxamic acids as selective inhibitors of class IIb histone deacetylases (HDACs).

Schäfer S, Saunders L, Eliseeva E, Velena A, Jung M, Schwienhorst A, Strasser A, Dickmanns A, Ficner R, Schlimme S, Sippl W, Verdin E, Jung M. Schäfer S, et al. Among authors: jung m. Bioorg Med Chem. 2008 Feb 15;16(4):2011-33. doi: 10.1016/j.bmc.2007.10.092. Epub 2007 Nov 4. Bioorg Med Chem. 2008. PMID: 18054239

7

Structure-activity studies on splitomicin derivatives as sirtuin inhibitors and computational prediction of binding mode.

Neugebauer RC, Uchiechowska U, Meier R, Hruby H, Valkov V, Verdin E, Sippl W, Jung M. Neugebauer RC, et al. Among authors: jung m. J Med Chem. 2008 Mar 13;51(5):1203-13. doi: 10.1021/jm700972e. Epub 2008 Feb 13. J Med Chem. 2008. PMID: 18269226

8

Assays for histone deacetylases.

Hauser AT, Jung M, Jung M. Hauser AT, et al. Among authors: jung m. Curr Top Med Chem. 2009;9(3):227-34. doi: 10.2174/156802609788085269. Curr Top Med Chem. 2009. PMID: 19355987 Review.

9

NAD(+) -dependent histone deacetylases (sirtuins) as novel therapeutic targets.

Schemies J, Uciechowska U, Sippl W, Jung M. Schemies J, et al. Among authors: jung m. Med Res Rev. 2010 Nov;30(6):861-89. doi: 10.1002/med.20178. Med Res Rev. 2010. PMID: 19824050 Review.

10

Novel 3-arylideneindolin-2-ones as inhibitors of NAD+ -dependent histone deacetylases (sirtuins).

Huber K, Schemies J, Uciechowska U, Wagner JM, Rumpf T, Lewrick F, Süss R, Sippl W, Jung M, Bracher F. Huber K, et al. Among authors: jung m. J Med Chem. 2010 Feb 11;53(3):1383-6. doi: 10.1021/jm901055u. J Med Chem. 2010. PMID: 20030343

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