Martin Neuenschwander

Dr.

Martin Neuenschwander

Chemical Biology


Screening-Unit


FMP

7,8-Dihydroxyflavone is a direct inhibitor of pyridoxal phosphatase

  • Brenner, M.; Zink, C.; Witzinger, L.; Keller, A.; Hadamek, K.; Bothe, S.; Neuenschwander, M.; Villmann, C.; von Kries, J.P.; Schindelin, H.; Jeanclos, E.; Gohla, A.

bioRxiv 2023

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An unconventional gatekeeper mutation sensitizes inositol hexakisphosphate kinases to an allosteric inhibitor

  • Aguirre, T.; Dornan, G.L.; Hostachy, S.; Neuenschwander, M.; Seyffarth, C.; Haucke, V.; Schütz, A.; von Kries, J.P.; Fiedler, D.

eLife 2023

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Structural Basis for Highly Selective Class II Alpha Phosphoinositide-3-Kinase Inhibition

  • Kücükdisli, M.; Bel-Abed, H.; Cirillo, D.; Lo, W.-T.; Efrém, N.-L.; Horatscheck, A.; Perepelittchenko, L.; Prokofeva, P.; Ehret, T.A.L.; Radetzki, S.; Neuenschwander, M.; Specker, E.; Médard, G.; Müller, S.; Wilhelm, S.; Kuster, B.; Von Kries, J.P.; Haucke, V.; Nazaré, M.

Journal of Medicinal Chemistry 2023

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Small Molecules Targeting Human UDP-GlcNAc 2-Epimerase

  • Gorenflos López, J.L.; Dornan, G.L.; Boback, N.; Neuenschwander, M.; Oder, A.; Kemnitz-Hassanin, K.; Schmieder, P.; Specker, E.; Asikoglu, H.C.; Oberdanner, C.; Seyffarth, C.; von Kries, J.P.; Lauster, D.; Hinderlich, S.; Hackenberger, C.P.R.

ChemBioChem 2023

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The FGFR inhibitor PD173074 binds to the C-terminus of oncofetal HMGA2 and modulates its DNA-binding and transcriptional activation functions

  • Ahmed, S.M.; Ragunathan, P.; Shin, J.; Peter, S.; Kleissle, S.; Neuenschwander, M.; Schäfer, R.; Kries, J.P.V.; Grüber, G.; Dröge, P.

FEBS Letters 2023

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Development of selective inhibitors of phosphatidylinositol 3-kinase C2α

  • Lo, W.-T.; Belabed, H.; Kücükdisli, M.; Metag, J.; Roske, Y.; Prokofeva, P.; Ohashi, Y.; Horatscheck, A.; Cirillo, D.; Krauss, M.; Schmied, C.; Neuenschwander, M.; von Kries, J.P.; Médard, G.; Kuster, B.; Perisic, O.; Williams, R.L.; Daumke, O.; Payrastre, B.; Severin, S.; Nazaré, M.; Haucke, V.

Nature Chemical Biology 2023

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CLK2 and CLK4 are regulators of DNA damage-induced NF-κB targeted by novel small molecule inhibitors

  • Mucka, P.; Lindemann, P.; Bosco, B.; Willenbrock, M.; Radetzki, S.; Neuenschwander, M.; Brischetto, C.; Peter von Kries, J.; Nazaré, M.; Scheidereit, C.

Cell Chemical Biology 2023

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Small molecule inhibiting microglial nitric oxide release could become a potential treatment for neuroinflammation

  • Jordan, P.; Costa, A.; Specker, E.; Popp, O.; Volkamer, A.; Piske, R.; Obrusnik, T.; Kleissle, S.; Stuke, K.; Rex, A.; Neuenschwander, M.; von Kries, J.P.; Nazare, M.; Mertins, P.; Kettenmann, H.; Wolf, S.A.

PLoS ONE 2023

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Drug discovery with an RBM20 dependent titin splice reporter identifies cardenolides as lead structures to improve cardiac filling

  • Liss, M.; Radke, M.H.; Eckhard, J.; Neuenschwander, M.; Dauksaite, V.; Von Kries, J.-P.; Gotthardt, M.

PLoS ONE 2018

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Use of a sequential high throughput screening assay to identify novel inhibitors of the eukaryotic SRP-Sec61 targeting/ translocation pathway

  • Klein, W.; Rutz, C.; Eckhard, J.; Provinciael, B.; Specker, E.; Neuenschwander, M.; Kleinau, G.; Scheerer, P.; Von Kries, J.-P.; Nazaré, M.; Vermeire, K.; Schülein, R.

PLoS ONE 2018

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Loss-of-function uORF mutations in human malignancies

  • Schulz, J.; Mah, N.; Neuenschwander, M.; Kischka, T.; Ratei, R.; Schlag, P.M.; Castaños-Vélez, E.; Fichtner, I.; Tunn, P.-U.; Denkert, C.; Klaas, O.; Berdel, W.E.; Von Kries, J.P.; Makalowski, W.; Andrade-Navarro, M.A.; Leutz, A.; Wethmar, K.

Scientific Reports 2018

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An AKAP-Lbc-RhoA interaction inhibitor promotes the translocation of aquaporin-2 to the plasma membrane of renal collecting duct principal cells

  • Schrade, K.; Tröger, J.; Eldahshan, A.; Zühlke, K.; Abdul Azeez, K.R.; Elkins, J.M.; Neuenschwander, M.; Oder, A.; Elkewedi, M.; Jaksch, S.; Andrae, K.; Li, J.; Fernandes, J.; Müller, P.M.; Grunwald, S.; Marino, S.F.; Vukićević, T.; Eichhorst, J.; Wiesner, B.; Weber, M.; Kapiloff, M.; Rocks, O.; Daumke, O.; Wieland, T.; Knapp, S.; Von Kries, J.P.; Klussmann, E.

PLoS ONE 2018

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Systematic pharmacological screens uncover novel pathways involved in cerebral cavernous malformations

  • Otten, C.; Knox, J.; Boulday, G.; Eymery, M.; Haniszewski, M.; Neuenschwander, M.; Radetzki, S.; Vogt, I.; Hähn, K.; De Luca, C.; Cardoso, C.; Hamad, S.; Igual Gil, C.; Roy, P.; Albiges-Rizo, C.; Faurobert, E.; von Kries, J.P.; Campillos, M.; Tournier-Lasserve, E.; Derry, W.B.; Abdelilah-Seyfried, S.

EMBO Molecular Medicine 2018

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Small-molecule inhibition of STOML3 oligomerization reverses pathological mechanical hypersensitivity

  • Wetzel, C.; Pifferi, S.; Picci, C.; Gök, C.; Hoffmann, D.; Bali, K.K.; Lampe, A.; Lapatsina, L.; Fleischer, R.; Smith, E.S.J.; Bégay, V.; Moroni, M.; Estebanez, L.; Kühnemund, J.; Walcher, J.; Specker, E.; Neuenschwander, M.; Von Kries, J.P.; Haucke, V.; Kuner, R.; Poulet, J.F.A.; Schmoranzer, J.; Poole, K.; Lewin, G.R.

Nature Neuroscience 2017

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Small Molecules Targeting Human N-Acetylmannosamine Kinase

  • Hinderlich, S.; Neuenschwander, M.; Wratil, P.R.; Oder, A.; Lisurek, M.; Nguyen, L.D.; von Kries, J.P.; Hackenberger, C.P.R.

ChemBioChem 2017

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Identification of a Novel Benzimidazole Pyrazolone Scaffold That Inhibits KDM4 Lysine Demethylases and Reduces Proliferation of Prostate Cancer Cells

  • Carter, D.M.; Specker, E.; Przygodda, J.; Neuenschwander, M.; von Kries, J.P.; Heinemann, U.; Nazaré, M.; Gohlke, U.

SLAS Discovery 2017

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A Chemical Disruptor of the ClpX Chaperone Complex Attenuates the Virulence of Multidrug-Resistant Staphylococcus aureus

  • Fetzer, C.; Korotkov, V.S.; Thänert, R.; Lee, K.M.; Neuenschwander, M.; von Kries, J.P.; Medina, E.; Sieber, S.A.

Angewandte Chemie - International Edition 2017

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Statin and rottlerin small-molecule inhibitors restrict colon cancer progression and metastasis via MACC1

  • Juneja, M.; Kobelt, D.; Walther, W.; Voss, C.; Smith, J.; Specker, E.; Neuenschwander, M.; Gohlke, B.-O.; Dahlmann, M.; Radetzki, S.; Preissner, R.; von Kries, J.P.; Schlag, P.M.; Stein, U.

PLoS Biology 2017

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Pharmacological restoration and therapeutic targeting of the B-cell phenotype in classical Hodgkin lymphoma

  • Du, J.; Neuenschwander, M.; Yu, Y.; Däbritz, J.H.M.; Neuendorff, N.-R.; Schleich, K.; Bittner, A.; Milanovic, M.; Beuster, G.; Radetzki, S.; Specker, E.; Reimann, M.; Rosenbauer, F.; Mathas, S.; Lohneis, P.; Hummel, M.; Dörken, B.; Von Kries, J.P.; Lee, S.; Schmitt, C.A.

Blood 2017

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