Publikationen von Herbert Waldmann

Niggemeyer, G.; Knyazeva, A.; Gasper, R.; Corkery, D.; Bodenbinder, P.-J.; Holstein, J. J.; Sievers, S.; Wu, Y.-W.; Waldmann, H.: Synthesis of 20-Membered Macrocyclic Pseudo-Natural Products Yields Inducers of LC3 Lipidation. Angewandte Chemie International Edition 61 (11), S. 1 - 21 (2022)

Niggemeyer, G.; Knyazeva, A.; Gasper, R.; Corkery, D.; Bodenbinder, P.-J.; Holstein, J. J.; Sievers, S.; Wu, Y.-W.; Waldmann, H.: Synthesis of 20-Membered Macrocyclic Pseudo-Natural Products Yields Inducers of LC3 Lipidation. Angewandte Chemie 134 (11), S. 1 - 21 (2022)

Grigalunas, M.; Brakmann, S.; Waldmann, H.: Chemical Evolution of Natural Product Structure. Journal of the American Chemical Society 144 (8), S. 3314 - 3329 (2022)

Akbarzadeh, M.; Flegel, J.; Patil, S.; Shang, E.; Narayan, R.; Buchholzer, M.; Jasemi, N. S. K.; Grigalunas, M.; Krzyzanowski, A.; Abegg, D. et al.; Shuster, A.; Potowski, M.; Karatas, H.; Karageorgis, G.; Mosaddeghzadeh, N.; Zischinsky, M.-L.; Merten, C.; Golz, C.; Brieger, L.; Strohmann, C.; Antonchick, A. P.; Janning, P.; Adibekian, A.; Goody, R. S.; Ahmadian, M. R.; Ziegler, S.; Waldmann, H.: The Pseudo-Natural Product Rhonin Targets RHOGDI. Angewandte Chemie International Edition, S. 1 - 27 (2022)

Akbarzadeh, M.; Flegel, J.; Patil, S.; Shang, E.; Narayan, R.; Buchholzer, M.; Jasemi, N. S. K.; Grigalunas, M.; Krzyzanowski, A.; Abegg, D. et al.; Shuster, A.; Potowski, M.; Karatas, H.; Karageorgis, G.; Mosaddeghzadeh, N.; Zischinsky, M.-L.; Merten, C.; Golz, C.; Brieger, L.; Strohmann, C.; Antonchick, A. P.; Janning, P.; Adibekian, A.; Goody, R. S.; Ahmadian, M. R.; Ziegler, S.; Waldmann, H.: The Pseudo-Natural Product Rhonin Targets RHOGDI. Angewandte Chemie, S. 1 - 27 (2022)

Yoshioka, H.; Kawamura, T.; Muroi, M.; Kondoh, Y.; Honda, K.; Kawatani, M.; Aono, H.; Waldmann, H.; Watanabe, N.; Osada, H.: Identification of a Small Molecule That Enhances Ferroptosis via Inhibition of Ferroptosis Suppressor Protein 1 (FSP1). ACS Chemical Biology, S. 1 - 9 (2022)

Wesseler, F.; Riege, D.; Puthanveedu, M.; Halver, J.; Müller, E.; Bertrand, J.; Antonchick, A. P.; Sievers, S.; Waldmann, H.; Schade, D.: Probing Embryonic Development Enables the Discovery of Unique Small-Molecule Bone Morphogenetic Protein Potentiators. Journal of Medicinal Chemistry, S. 1 - 13 (2022)

Shaaban, S.; Merten, C.; Waldmann, H.: Catalytic Atroposelective C7-Functionalisation of Indolines and Indoles. Chem. Eur. J. 28 (1) (2022)

Akbarzadeh, M.; Deipenwisch, I.; Schoelermann, B.; Pahl, A.; Sievers, S.; Ziegler, S.; Waldmann, H.: Morphological profiling by means of the Cell Painting assay enables identification of tubulin-targeting compounds. Cell Chemical Biology, S. 1 - 16 (2021)

Carnero Corrales, M. A.; Zinken, S.; Konstantinidis, G.; Rafehi, M.; Abdelrahman, A.; Wu, Y.-W.; Janning, P.; Müller, C. E.; Laraia, L.; Waldmann, H.: Thermal proteome profiling identifies the membrane-bound purinergic receptor P2X4 as a target of the autophagy inhibitor indophagolin. Cell Chemical Biology 28 (12), S. 1750 - 1757 (2021)

Schneidewind, T.; Brause, A.; Schölermann, B.; Sievers, S.; Pahl, A.; Sankar, M. G.; Winzker, M.; Janning, P.; Kumar, K.; Ziegler, S. et al.; Waldmann, H.: Combined morphological and proteome profiling reveals target-independent impairment of cholesterol homeostasis. Cell Chemical Biology 28 (12), S. 1780 - 1794 (2021)

Shaaban, S.; Merten, C.; Waldmann, H.: Catalytic Atroposelective C7-Functionalisation of Indolines and Indoles. Chemistry – A European Journal 28 (1), S. 1 - 7 (2021)

Gally, J.-M.; Pahl, A.; Czodrowski, P.; Waldmann, H.: Pseudonatural Products Occur Frequently in Biologically Relevant Compounds. Journal of Chemical Information and Modeling 61 (11), S. 5458 - 5468 (2021)

Burhop, A.; Bag, S.; Grigalunas, M.; Woitalla, S.; Bodenbinder, P.-J.; Brieger, L.; Strohmann, C.; Pahl, A.; Sievers, S.; Waldmann, H.: Synthesis of Indofulvin Pseudo-Natural Products Yields a New Autophagy Inhibitor Chemotype. Advanced Science 8 (19), e2102042, S. 1 - 10 (2021)

Liu, J.; Flegel, J.; Otte, F.; Pahl, A.; Sievers, S.; Strohmann, C.; Waldmann, H.: Combination of Pseudo-Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo-Sesquiterpenoid Alkaloids. Angewandte Chemie International Edition 60 (39), S. 21384 - 21395 (2021)

Liu, J.; Flegel, J.; Otte, F.; Pahl, A.; Sievers, S.; Strohmann, C.; Waldmann, H.: Combination of Pseudo-Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo-Sesquiterpenoid Alkaloids. Angewandte Chemie 133 (39), S. 21554 - 21565 (2021)

Yildirim, O.; Grigalunas, M.; Brieger, L.; Strohmann, C.; Antonchick, A. P.; Waldmann, H.: Dynamic Catalytic Highly Enantioselective 1,3-Dipolar Cycloadditions. Angewandte Chemie International Edition 60 (36), S. 20012 - 20020 (2021)

Yildirim, O.; Grigalunas, M.; Brieger, L.; Strohmann, C.; Antonchick, A. P.; Waldmann, H.: Dynamic Catalytic Highly Enantioselective 1,3-Dipolar Cycloadditions. Angewandte Chemie 133 (36), S. 20165 - 20173 (2021)

Liu, J.; Otte, F.; Strohmann, C.; Waldmann, H.: Enantioselective synthesis of pyrro[3,4-c]quinoline pseudo-natural products. Tetrahedron Letters 76, 153228, S. 1 - 4 (2021)

Karageorgis, G.; Foley, D. J.; Laraia, L.; Brakmann, S.; Waldmann, H.: Pseudo Natural Products – Chemical Evolution of Natural Product Structure. Angewandte Chemie International Edition 60 (29), S. 15705 - 15723 (2021)