39 results on '"Llona-Minguez, Sabin"'
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2. Pharmacological targeting of MTHFD2 suppresses acute myeloid leukemia by inducing thymidine depletion and replication stress
3. Synthesis of Substituted Indazole Acetic Acids by N‐N Bond Forming Reactions
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
15. Tetrahydrobenzothiophene carboxamides: Beyond the kinase domain and into the fatty acid realm
16. Diverse heterocyclic scaffolds as dCTP pyrophosphatase 1 inhibitors. Part 1: Triazoles, triazolopyrimidines, triazinoindoles, quinoline hydrazones and arylpiperazines
17. Diverse heterocyclic scaffolds as dCTP pyrophosphatase 1 inhibitors. Part 2: Pyridone- and pyrimidinone-derived systems
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
28. Novel spirocyclic systems via multicomponent aza-Diels–Alder reaction
29. Structure–metabolism-relationships in the microsomal clearance of piperazin-1-ylpyridazines
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).
35. ChemInform Abstract: Vinylic MIDA Boronates: New Building Blocks for the Synthesis of Aza-Heterocycles.
36. Lysophosphatidic acid receptor (LPAR) modulators: The current pharmacological toolbox
37. Vinylic MIDA Boronates: New Building Blocks for the Synthesis of Aza‐Heterocycles
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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