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Your search keyword '"Llona-Minguez, Sabin"' showing total 39 results

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39 results on '"Llona-Minguez, Sabin"'

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1. Identification and evaluation of small-molecule inhibitors against the dNTPase SAMHD1 via a comprehensive screening funnel

2. Pharmacological targeting of MTHFD2 suppresses acute myeloid leukemia by inducing thymidine depletion and replication stress

4. Supplementary Table S2 from Crystal Structure of the Emerging Cancer Target MTHFD2 in Complex with a Substrate-Based Inhibitor

5. Supplementary Methods and References from Crystal Structure of the Emerging Cancer Target MTHFD2 in Complex with a Substrate-Based Inhibitor

6. Supplementary Figures S1-S7 from Crystal Structure of the Emerging Cancer Target MTHFD2 in Complex with a Substrate-Based Inhibitor

7. Data from Crystal Structure of the Emerging Cancer Target MTHFD2 in Complex with a Substrate-Based Inhibitor

8. Synthesis of Substituted Indazole Acetic Acids by N-N Bond Forming Reactions

9. Author Correction: Targeted NUDT5 inhibitors block hormone signaling in breast cancer cells

10. Identification and evaluation of small-molecule inhibitors against the dNTPase SAMHD1viaa comprehensive screening funnel

11. Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions.

12. Targeted NUDT5 inhibitors block hormone signaling in breast cancer cells

13. Supplementary methods for "Pharmacological targeting of MTHFD2 suppresses acute myeloid leukemia by inducing thymidine depletion and replication stress"

14. Inhibitory Kappa B Kinase α (IKKα) Inhibitors That Recapitulate Their Selectivity in Cells against Isoform-Related Biomarkers

18. Structure–metabolism-relationships in the microsomal clearance of piperazin-1-ylpyridazines† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7md00230k

19. Identification of Triazolothiadiazoles as Potent Inhibitors of the dCTP Pyrophosphatase 1

20. Piperazin-1-ylpyridazine Derivatives Are a Novel Class of Human dCTP Pyrophosphatase 1 Inhibitors

21. Structure-metabolism-relationships in the microsomal clearance of piperazin-1-ylpyridazines

22. Crystal Structure of the Emerging Cancer Target MTHFD2 in Complex with a Substrate-Based Inhibitor

23. Novel spirocyclic systems via multicomponent aza-Diels-Alder reaction

24. Correction to Piperazin-1-ylpyridazine Derivatives Are a Novel Class of Human dCTP Pyrophosphatase 1 Inhibitors

25. Piperazin-1-ylpyridazine Derivatives Are a Novel Class of Human dCTP Pyrophosphatase 1 Inhibitors

26. Identification of Triazolothiadiazoles as Potent Inhibitors of the dCTP Pyrophosphatase 1

27. Crystal Structure of the Emerging Cancer Target MTHFD2 in Complex with a Substrate-Based Inhibitor

30. Correction to Piperazin-1-ylpyridazine Derivatives Are a Novel Class of Human dCTP Pyrophosphatase 1 Inhibitors

31. Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1

32. Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1

33. Vinylic MIDA Boronates : New Building Blocks for the Synthesis of Aza-Heterocycles

34. Front Cover: Synthesis of Substituted Indazole Acetic Acids by N−N Bond Forming Reactions (Eur. J. Org. Chem. 29/2023).

38. Inhibitory Kappa B Kinase α (IKKα) Inhibitors That Recapitulate Their Selectivity in Cells against Isoform-Related Biomarkers.

39. Vinylic MIDA Boronates: New Building Blocks for the Synthesis of Aza-Heterocycles.

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