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Michael Gütschow
Michael Gütschow
在 uni-bonn.de 的电子邮件经过验证
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引用次数
引用次数
年份
Recent developments in hydantoin chemistry. A review
M Meusel, M Gütschow
Organic preparations and procedures international 36 (5), 391-443, 2004
3142004
Degradation of Quercetin and Luteolin byEubacterium ramulus
A Braune, M Gütschow, W Engst, M Blaut
Applied and environmental microbiology 67 (12), 5558-5567, 2001
2642001
Conversion of daidzein and genistein by an anaerobic bacterium newly isolated from the mouse intestine
A Matthies, T Clavel, M Gütschow, W Engst, D Haller, M Blaut, A Braune
Applied and environmental microbiology 74 (15), 4847-4852, 2008
1842008
Dysfunction of the key ferroptosis-surveilling systems hypersensitizes mice to tubular necrosis during acute kidney injury
W Tonnus, C Meyer, C Steinebach, A Belavgeni, A von Mässenhausen, ...
Nature communications 12 (1), 4402, 2021
1512021
Calcium-sensing receptors signal constitutive macropinocytosis and facilitate the uptake of NOD2 ligands in macrophages
J Canton, D Schlam, C Breuer, M Gütschow, M Glogauer, S Grinstein
Nature communications 7 (1), 11284, 2016
1472016
Homo-PROTACs for the chemical knockdown of cereblon
C Steinebach, S Lindner, ND Udeshi, DC Mani, H Kehm, S Köpff, ...
ACS chemical biology 13 (9), 2771-2782, 2018
1352018
Interaction of papain-like cysteine proteases with dipeptide-derived nitriles
R Löser, K Schilling, E Dimmig, M Gütschow
Journal of medicinal chemistry 48 (24), 7688-7707, 2005
1322005
2-(Diethylamino) thieno [1, 3] oxazin-4-ones as stable inhibitors of human leukocyte elastase
M Gütschow, L Kuerschner, U Neumann, M Pietsch, R Löser, N Koglin, ...
Journal of medicinal chemistry 42 (26), 5437-5447, 1999
1321999
Regulation of TMPRSS6 by BMP6 and iron in human cells and mice
D Meynard, V Vaja, CC Sun, E Corradini, S Chen, C López-Otín, ...
Blood, The Journal of the American Society of Hematology 118 (3), 747-756, 2011
1312011
Development of nitrile-based peptidic inhibitors of cysteine cathepsins
M Frizler, M Stirnberg, MT Sisay, M Gutschow
Current topics in medicinal chemistry 10 (3), 294-322, 2010
1262010
Synthesis of tricyclic 1, 3-oxazin-4-ones and kinetic analysis of cholesterol esterase and acetylcholinesterase inhibition
M Pietsch, M Gütschow
Journal of medicinal chemistry 48 (26), 8270-8288, 2005
1242005
Antimicrobial phenalenone derivatives from the marine-derived fungus Coniothyrium cereale
MF Elsebai, S Kehraus, U Lindequist, F Sasse, S Shaaban, M Gütschow, ...
Organic & Biomolecular Chemistry 9 (3), 802-808, 2011
1222011
E3 ligase ligands in successful PROTACs: an overview of syntheses and linker attachment points
A Bricelj, C Steinebach, R Kuchta, M Gütschow, I Sosič
Frontiers in chemistry 9, 707317, 2021
1212021
Analogs of thalidomide as potential angiogenesis inhibitors
WD Figg, K Eger, U Teubert, M Weiss, M Guetschow, T Hecker, ...
US Patent 7,320,991, 2008
1212008
Antiangiogenic activity of N-substituted and tetrafluorinated thalidomide analogues
SSW Ng, M Gütschow, M Weiss, S Hauschildt, U Teubert, TK Hecker, ...
Cancer research 63 (12), 3189-3194, 2003
1132003
3CL protease inhibitors with an electrophilic arylketone moiety as anti-SARS-CoV-2 agents
S Konno, K Kobayashi, M Senda, Y Funai, Y Seki, I Tamai, L Schäkel, ...
Journal of Medicinal Chemistry 65 (4), 2926-2939, 2021
1112021
Targeting the main protease of SARS‐CoV‐2: from the establishment of high throughput screening to the design of tailored inhibitors
J Breidenbach, C Lemke, T Pillaiyar, L Schäkel, G Al Hamwi, M Diett, ...
Angewandte Chemie International Edition 60 (18), 10423-10429, 2021
1102021
Structural optimization of azadipeptide nitriles strongly increases association rates and allows the development of selective cathepsin inhibitors
M Frizler, F Lohr, N Furtmann, J Kläs, M Gütschow
Journal of medicinal chemistry 54 (1), 396-400, 2011
1012011
Systematic exploration of different E3 ubiquitin ligases: an approach towards potent and selective CDK6 degraders
C Steinebach, YLD Ng, I Sosič, CS Lee, S Chen, S Lindner, LP Vu, ...
Chemical science 11 (13), 3474-3486, 2020
982020
Azadipeptide nitriles: highly potent and proteolytically stable inhibitors of papain‐like cysteine proteases
R Löser, M Frizler, K Schilling, M Gütschow
Angewandte Chemie International Edition 47 (23), 4331-4334, 2008
962008
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