Jauch J - Search Results

1

Myrtucommulone-A Induces both Extrinsic and Intrinsic Apoptotic Pathways in Cancer Cells.

Izgi K, Iskender B, Jauch J, Sezen S, Cakir M, Charpentier M, Canatan H, Sakalar C. Izgi K, et al. Among authors: jauch j. J Biochem Mol Toxicol. 2015 Sep;29(9):432-439. doi: 10.1002/jbt.21716. Epub 2015 Jun 2. J Biochem Mol Toxicol. 2015. PMID: 26032814

2

Inhibition of epithelial-mesenchymal transition in bladder cancer cells via modulation of mTOR signalling.

Iskender B, Izgi K, Hizar E, Jauch J, Arslanhan A, Yuksek EH, Canatan H. Iskender B, et al. Among authors: jauch j. Tumour Biol. 2016 Jun;37(6):8281-91. doi: 10.1007/s13277-015-4695-1. Epub 2015 Dec 30. Tumour Biol. 2016. PMID: 26718217

3

Stereoisomeric Composition of Natural Myrtucommulone A.

Hans M, Charpentier M, Huch V, Jauch J, Bruhn T, Bringmann G, Quandt D. Hans M, et al. Among authors: jauch j. J Nat Prod. 2015 Oct 23;78(10):2381-9. doi: 10.1021/acs.jnatprod.5b00358. Epub 2015 Oct 12. J Nat Prod. 2015. PMID: 26457652

4

Total synthesis of myrtucommulone A.

Müller H, Paul M, Hartmann D, Huch V, Blaesius D, Koeberle A, Werz O, Jauch J. Müller H, et al. Among authors: jauch j. Angew Chem Int Ed Engl. 2010 Mar 8;49(11):2045-9. doi: 10.1002/anie.200903906. Angew Chem Int Ed Engl. 2010. PMID: 20155764 No abstract available.

5

The acylphloroglucinols hyperforin and myrtucommulone A cause mitochondrial dysfunctions in leukemic cells by direct interference with mitochondria.

Wiechmann K, Müller H, Fischer D, Jauch J, Werz O. Wiechmann K, et al. Among authors: jauch j. Apoptosis. 2015 Nov;20(11):1508-17. doi: 10.1007/s10495-015-1170-9. Apoptosis. 2015. PMID: 26386573

6

Mitochondrial Chaperonin HSP60 Is the Apoptosis-Related Target for Myrtucommulone.

Wiechmann K, Müller H, König S, Wielsch N, Svatoš A, Jauch J, Werz O. Wiechmann K, et al. Among authors: jauch j. Cell Chem Biol. 2017 May 18;24(5):614-623.e6. doi: 10.1016/j.chembiol.2017.04.008. Epub 2017 Apr 28. Cell Chem Biol. 2017. PMID: 28457707 Free article.

7

Efficient preparation of incensole and incensole acetate, and quantification of these bioactive diterpenes in Boswellia papyrifera by a RP-DAD-HPLC method.

Paul M, Jauch J. Paul M, et al. Among authors: jauch j. Nat Prod Commun. 2012 Mar;7(3):283-8. Nat Prod Commun. 2012. PMID: 22545396

8

Synthesis and biological evaluation of novel myrtucommulones and structural analogues that target mPGES-1 and 5-lipoxygenase.

Wiechmann K, Müller H, Huch V, Hartmann D, Werz O, Jauch J. Wiechmann K, et al. Among authors: jauch j. Eur J Med Chem. 2015 Aug 28;101:133-49. doi: 10.1016/j.ejmech.2015.06.001. Epub 2015 Jun 5. Eur J Med Chem. 2015. PMID: 26123643

9

A thin-layer chromatography method for the identification of three different olibanum resins (Boswellia serrata, Boswellia papyrifera and Boswellia carterii, respectively, Boswellia sacra).

Paul M, Brüning G, Bergmann J, Jauch J. Paul M, et al. Among authors: jauch j. Phytochem Anal. 2012 Mar-Apr;23(2):184-9. doi: 10.1002/pca.1341. Epub 2011 Aug 20. Phytochem Anal. 2012. PMID: 21858880

10

Total synthesis of azadirachtin--finally completed after 22 years.

Jauch J. Jauch J. Angew Chem Int Ed Engl. 2008;47(1):34-7. doi: 10.1002/anie.200703814. Angew Chem Int Ed Engl. 2008. PMID: 17966967 No abstract available.

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