Loesche A - Search Results

1

Synthesis and cholinesterase inhibiting potential of A-ring azepano- and 3-amino-3,4-seco-triterpenoids.

Kazakova O, Smirnova I, Lopatina T, Giniyatullina G, Petrova A, Khusnutdinova E, Csuk R, Serbian I, Loesche A. Kazakova O, et al. Among authors: loesche a. Bioorg Chem. 2020 Aug;101:104001. doi: 10.1016/j.bioorg.2020.104001. Epub 2020 Jun 10. Bioorg Chem. 2020. PMID: 32683137

2

Converting maslinic acid into an effective inhibitor of acylcholinesterases.

Schwarz S, Loesche A, Lucas SD, Sommerwerk S, Serbian I, Siewert B, Pianowski E, Csuk R. Schwarz S, et al. Among authors: loesche a. Eur J Med Chem. 2015 Oct 20;103:438-45. doi: 10.1016/j.ejmech.2015.09.007. Epub 2015 Sep 9. Eur J Med Chem. 2015. PMID: 26383128

3

Amino derivatives of platanic acid act as selective and potent inhibitors of butyrylcholinesterase.

Heller L, Kahnt M, Loesche A, Grabandt P, Schwarz S, Brandt W, Csuk R. Heller L, et al. Among authors: loesche a. Eur J Med Chem. 2017 Jan 27;126:652-668. doi: 10.1016/j.ejmech.2016.11.056. Epub 2016 Nov 30. Eur J Med Chem. 2017. PMID: 27936444

4

Novel dehydroabietylamine derivatives as potent inhibitors of acetylcholinesterase.

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

5

Unexpected AChE inhibitory activity of (2E)α,β-unsaturated fatty acids.

Loesche A, Wiemann J, Al Halabi Z, Karasch J, Sippl W, Csuk R. Loesche A, et al. Bioorg Med Chem Lett. 2018 Nov 1;28(20):3315-3319. doi: 10.1016/j.bmcl.2018.09.013. Epub 2018 Sep 11. Bioorg Med Chem Lett. 2018. PMID: 30220607

6

Ursolic and oleanolic acid derivatives with cholinesterase inhibiting potential.

Loesche A, Köwitsch A, Lucas SD, Al-Halabi Z, Sippl W, Al-Harrasi A, Csuk R. Loesche A, et al. Bioorg Chem. 2019 Apr;85:23-32. doi: 10.1016/j.bioorg.2018.12.013. Epub 2018 Dec 15. Bioorg Chem. 2019. PMID: 30599410

7

Triterpene-Based Carboxamides Act as Good Inhibitors of Butyrylcholinesterase.

Loesche A, Kahnt M, Serbian I, Brandt W, Csuk R. Loesche A, et al. Molecules. 2019 Mar 7;24(5):948. doi: 10.3390/molecules24050948. Molecules. 2019. PMID: 30866589 Free PMC article.

8

Caffeic acid phenethyl ester (CAPE)-derivatives act as selective inhibitors of acetylcholinesterase.

Gießel JM, Loesche A, Csuk R, Serbian I. Gießel JM, et al. Among authors: loesche a. Eur J Med Chem. 2019 Sep 1;177:259-268. doi: 10.1016/j.ejmech.2019.05.059. Epub 2019 May 26. Eur J Med Chem. 2019. PMID: 31158743

9

Substituted cinnamic anhydrides act as selective inhibitors of acetylcholinesterase.

Gießel JM, Serbian I, Loesche A, Csuk R. Gießel JM, et al. Among authors: loesche a. Bioorg Chem. 2019 Sep;90:103058. doi: 10.1016/j.bioorg.2019.103058. Epub 2019 Jun 8. Bioorg Chem. 2019. PMID: 31212181

10

Novel 12-hydroxydehydroabietylamine derivatives act as potent and selective butyrylcholinesterase inhibitors.

Loesche A, Wiemann J, Rohmer M, Brandt W, Csuk R. Loesche A, et al. Bioorg Chem. 2019 Sep;90:103092. doi: 10.1016/j.bioorg.2019.103092. Epub 2019 Jul 2. Bioorg Chem. 2019. PMID: 31280014

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