A. Krzyzanowski

发表

Hot-spot guided design of macrocyclic inhibitors of the LSD1-CoREST1 interaction

H. Waldmann, H. Adihou, Peter ‘t Hart, 2019, Tetrahedron.

Synthesis of Indole-, Benzo[ b]thiophene-, and Benzo[ b]selenophene-Based Analogues of the Resveratrol Dimers Viniferifuran and (±)-Dehydroampelopsin B.

M. Elofsson, Michael Saleeb, A. Krzyzanowski, 2018, Organic letters.

Development of Macrocyclic PRMT5–Adaptor Protein Interaction Inhibitors

H. Waldmann, R. Prudent, C. Peter, 2022, Journal of medicinal chemistry.

Structure Based Design of Bicyclic Peptide Inhibitors of RbAp48

I. Vetter, H. Waldmann, H. Adihou, 2020, Angewandte Chemie.

The Highly Potent AhR Agonist Picoberin Modulates Hh-Dependent Osteoblast Differentiation

H. Waldmann, D. Schade, F. Rastinejad, 2022, Journal of medicinal chemistry.

Total Synthesis of Viniferifuran and Dehydroampelopsin B Analogues

A. Krzyzanowski, 2018 .

Unprecedented Combination of Polyketide Natural Product Fragments Identifies the New Hedgehog Signaling Pathway Inhibitor Grismonone

H. Waldmann, Slava Ziegler, B. Schölermann, 2022, Chemistry.

Biochemical Investigation of the Interaction of pICln, RioK1 and COPR5 with the PRMT5–MEP50 Complex

H. Waldmann, H. Adihou, R. Gasper, 2021, Chembiochem : a European journal of chemical biology.

Spacial Score—A Comprehensive Topological Indicator for Small-Molecule Complexity

A. Pahl, A. Krzyzanowski, Michael Grigalunas, 2023, Journal of medicinal chemistry.