Kupfer E - Search Results

1

Lipstatin, an inhibitor of pancreatic lipase, produced by Streptomyces toxytricini. II. Chemistry and structure elucidation.

Hochuli E, Kupfer E, Maurer R, Meister W, Mercadal Y, Schmidt K. Hochuli E, et al. Among authors: kupfer e. J Antibiot (Tokyo). 1987 Aug;40(8):1086-91. doi: 10.7164/antibiotics.40.1086. J Antibiot (Tokyo). 1987. PMID: 3680019 Free article.

2

Anantin--a peptide antagonist of the atrial natriuretic factor (ANF). I. Producing organism, fermentation, isolation and biological activity.

Weber W, Fischli W, Hochuli E, Kupfer E, Weibel EK. Weber W, et al. Among authors: kupfer e. J Antibiot (Tokyo). 1991 Feb;44(2):164-71. doi: 10.7164/antibiotics.44.164. J Antibiot (Tokyo). 1991. PMID: 1849131 Free article.

3

Lipstatin, an inhibitor of pancreatic lipase, produced by Streptomyces toxytricini. I. Producing organism, fermentation, isolation and biological activity.

Weibel EK, Hadvary P, Hochuli E, Kupfer E, Lengsfeld H. Weibel EK, et al. Among authors: kupfer e. J Antibiot (Tokyo). 1987 Aug;40(8):1081-5. doi: 10.7164/antibiotics.40.1081. J Antibiot (Tokyo). 1987. PMID: 3680018 Free article.

4

Tracer studies with crude U-13C-lipid mixtures. Biosynthesis of the lipase inhibitor lipstatin.

Eisenreich W, Kupfer E, Weber W, Bacher A. Eisenreich W, et al. Among authors: kupfer e. J Biol Chem. 1997 Jan 10;272(2):867-74. doi: 10.1074/jbc.272.2.867. J Biol Chem. 1997. PMID: 8995375 Free article.

5

Biosynthetic origin of a branched chain analogue of the lipase inhibitor, lipstatin.

Eisenreich W, Kupfer E, Stohler P, Weber W, Bacher A. Eisenreich W, et al. Among authors: kupfer e. J Med Chem. 2003 Sep 11;46(19):4209-12. doi: 10.1021/jm030780x. J Med Chem. 2003. PMID: 12954074

6

Biosynthetic precursors of the lipase inhibitor lipstatin.

Schuhr CA, Eisenreich W, Goese M, Stohler P, Weber W, Kupfer E, Bacher A. Schuhr CA, et al. Among authors: kupfer e. J Org Chem. 2002 Apr 5;67(7):2257-62. doi: 10.1021/jo016285v. J Org Chem. 2002. PMID: 11925237

7

Biosynthetic origin of hydrogen atoms in the lipase inhibitor lipstatin.

Goese M, Eisenreich W, Kupfer E, Weber W, Bacher A. Goese M, et al. Among authors: kupfer e. J Biol Chem. 2000 Jul 14;275(28):21192-6. doi: 10.1074/jbc.M003094200. J Biol Chem. 2000. PMID: 10801870 Free article.

8

Large scale preparation of chiral building blocks for the P3 site of renin inhibitors.

Doswald S, Estermann H, Kupfer E, Stadler H, Walther W, Weisbrod T, Wirz B, Wostl W. Doswald S, et al. Among authors: kupfer e. Bioorg Med Chem. 1994 Jun;2(6):403-10. doi: 10.1016/0968-0896(94)80007-3. Bioorg Med Chem. 1994. PMID: 8000860

9

Metabolite identification via LC-SPE-NMR-MS of the in vitro biooxidation products of a lead mGlu5 allosteric antagonist and impact on the improvement of metabolic stability in the series.

Ceccarelli SM, Schlotterbeck G, Boissin P, Binder M, Buettelmann B, Hanlon S, Jaeschke G, Kolczewski S, Kupfer E, Peters JU, Porter RH, Prinssen EP, Rueher M, Ruf I, Spooren W, Stämpfli A, Vieira E. Ceccarelli SM, et al. Among authors: kupfer e. ChemMedChem. 2008 Jan;3(1):136-44. doi: 10.1002/cmdc.200700203. ChemMedChem. 2008. PMID: 17994660

10

Biosynthesis of lipstatin. Incorporation of multiply deuterium-labeled (5Z,8Z)-tetradeca-5,8-dienoic acid and octanoic acid.

Goese M, Eisenreich W, Kupfer E, Stohler P, Weber W, Leuenberger HG, Bacher A. Goese M, et al. Among authors: kupfer e. J Org Chem. 2001 Jun 29;66(13):4673-8. doi: 10.1021/jo010230b. J Org Chem. 2001. PMID: 11421791

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