Wiemann J - Search Results

1

Amino(oxo)acetate moiety: A new functional group to improve the cytotoxicity of betulin derived carbamates.

Heller L, Perl V, Wiemann J, Al-Harrasi A, Csuk R. Heller L, et al. Among authors: wiemann j. Bioorg Med Chem Lett. 2016 Jun 15;26(12):2852-2854. doi: 10.1016/j.bmcl.2016.04.055. Epub 2016 Apr 20. Bioorg Med Chem Lett. 2016. PMID: 27142753

2

A bioassay-driven discovery of an unexpected selenophene and its cytotoxicity.

Csuk R, Siewert B, Wiemann J. Csuk R, et al. Among authors: wiemann j. Bioorg Med Chem Lett. 2013 Jun 15;23(12):3542-6. doi: 10.1016/j.bmcl.2013.04.036. Epub 2013 Apr 23. Bioorg Med Chem Lett. 2013. PMID: 23664875

3

The chemical and biological potential of C ring modified triterpenoids.

Siewert B, Wiemann J, Köwitsch A, Csuk R. Siewert B, et al. Among authors: wiemann j. Eur J Med Chem. 2014 Jan 24;72:84-101. doi: 10.1016/j.ejmech.2013.11.025. Epub 2013 Dec 5. Eur J Med Chem. 2014. PMID: 24361521

4

Betulinic acid derived hydroxamates and betulin derived carbamates are interesting scaffolds for the synthesis of novel cytotoxic compounds.

Wiemann J, Heller L, Perl V, Kluge R, Ströhl D, Csuk R. Wiemann J, et al. Eur J Med Chem. 2015 Dec 1;106:194-210. doi: 10.1016/j.ejmech.2015.10.043. Epub 2015 Nov 5. Eur J Med Chem. 2015. PMID: 26547057

5

First Occurrence of a Furano-glycyrrhetinoate and Its Cytotoxicity.

Heller L, Sommerwerk S, Tzschöckell F, Wiemann J, Schwarz S, Siewert B, Al-Harrasi A, Csuk R. Heller L, et al. Among authors: wiemann j. Arch Pharm (Weinheim). 2015 Dec;348(12):889-96. doi: 10.1002/ardp.201500318. Epub 2015 Nov 9. Arch Pharm (Weinheim). 2015. PMID: 26548762

6

Targeting cancer cells with oleanolic and ursolic acid derived hydroxamates.

Wiemann J, Heller L, Csuk R. Wiemann J, et al. Bioorg Med Chem Lett. 2016 Feb 1;26(3):907-909. doi: 10.1016/j.bmcl.2015.12.064. Epub 2015 Dec 19. Bioorg Med Chem Lett. 2016. PMID: 26750249

7

Synthesis and proapoptotic activity of oleanolic acid derived amides.

Heller L, Knorrscheidt A, Flemming F, Wiemann J, Sommerwerk S, Pavel IZ, Al-Harrasi A, Csuk R. Heller L, et al. Among authors: wiemann j. Bioorg Chem. 2016 Oct;68:137-51. doi: 10.1016/j.bioorg.2016.08.004. Epub 2016 Aug 6. Bioorg Chem. 2016. PMID: 27518757

8

Novel dehydroabietylamine derivatives as potent inhibitors of acetylcholinesterase.

Wiemann J, Loesche A, Csuk R. Wiemann J, et al. Bioorg Chem. 2017 Oct;74:145-157. doi: 10.1016/j.bioorg.2017.07.013. Epub 2017 Aug 1. Bioorg Chem. 2017. PMID: 28797788

9

Piperlongumine B and analogs are promising and selective inhibitors for acetylcholinesterase.

Wiemann J, Karasch J, Loesche A, Heller L, Brandt W, Csuk R. Wiemann J, et al. Eur J Med Chem. 2017 Oct 20;139:222-231. doi: 10.1016/j.ejmech.2017.07.081. Epub 2017 Aug 2. Eur J Med Chem. 2017. PMID: 28802122

10

An access to a library of novel triterpene derivatives with a promising pharmacological potential by Ugi and Passerini multicomponent reactions.

Wiemann J, Heller L, Csuk R. Wiemann J, et al. Eur J Med Chem. 2018 Apr 25;150:176-194. doi: 10.1016/j.ejmech.2018.02.060. Epub 2018 Feb 21. Eur J Med Chem. 2018. PMID: 29529499

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