Wiemann J - Search Results

1

Cytotoxic Dehydroabietylamine Derived Compounds.

Wiemann J, Al-Harrasi A, Csuk R. Wiemann J, et al. Anticancer Agents Med Chem. 2020;20(15):1756-1767. doi: 10.2174/1871520620666200317110010. Anticancer Agents Med Chem. 2020. PMID: 32183684 Review.

2

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

3

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

4

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

5

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

6

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

7

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

8

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

9

Syntheses of C-ring modified dehydroabietylamides and their cytotoxic activity.

Wiemann J, Fischer L, Rohmer M, Csuk R. Wiemann J, et al. Eur J Med Chem. 2018 Aug 5;156:861-870. doi: 10.1016/j.ejmech.2018.07.051. Epub 2018 Jul 20. Eur J Med Chem. 2018. PMID: 30056282

10

Ugi multicomponent-reaction: Syntheses of cytotoxic dehydroabietylamine derivatives.

Wiemann J, Fischer Née Heller L, Kessler J, Ströhl D, Csuk R. Wiemann J, et al. Bioorg Chem. 2018 Dec;81:567-576. doi: 10.1016/j.bioorg.2018.09.014. Epub 2018 Sep 11. Bioorg Chem. 2018. PMID: 30248508

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