| Autor: |
Ceballos, J, Schwalfenberg, M, Karageorgis, G, Reckzeh, ES, Sievers, S, Ostermann, C, Pahl, A, Sellstedt, M, Nowacki, J, Carnero Corrales, MA, Wilke, J, Laraia, L, Tschapalda, K, Metz, M, Sehr, DA, Brand, S, Winklhofer, K, Janning, P, Ziegler, S, Waldmann, H |
| Jazyk: |
angličtina |
| Rok vydání: |
2019 |
| ISSN: |
1433-7851 |
| Popis: |
Bioactive compound design based on natural product (NP) structure may be limited due to partial coverage of NP‐like chemical space and biological target space. These limitations can be overcome by combining NP‐centered strategies with fragment‐based compound design through combination of NP‐derived fragments to structurally unprecedented “pseudo natural products” (pseudo‐NPs). We describe the design, synthesis and biological evaluation of a collection of indomorphan pseudo‐NPs that combine biosynthetically unrelated indole‐ and morphan‐alkaloid fragments. Biological investigation in a cell‐based screen for modulators of glucose uptake identified the indomorphane derivative Glupin as potent inhibitor of glucose uptake. Glupin selectively targets and upregulates both, glucose transporters GLUT‐1 and GLUT‐3. Glupin suppresses glycolysis, reduces the levels of glucose‐derived metabolites and attenuates the growth of various cancer cell lines. Our findings underscore the importance of dual GLUT‐1 and GLUT‐3 inhibition to efficiently suppress tumor cell growth and the cellular rescue mechanism, which counteracts glucose scarcity. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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