33 results on '"Cao, Danyan"'
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2. Structure-Based Rational Design and Evaluation of BET-Aurora Kinase Dual-Inhibitors for Treatment of Cancers.
3. Multi-omics characterization of WNT pathway reactivation to ameliorate BET inhibitor resistance in liver cancer cells
4. Fragment-based drug discovery of triazole inhibitors to block PDEδ-RAS protein-protein interaction
5. Structure-based optimization of a series of selective BET inhibitors containing aniline or indoline groups
6. Discovery of a series of dihydroquinoxalin-2(1H)-ones as selective BET inhibitors from a dual PLK1-BRD4 inhibitor
7. Structure, magnetic and transport properties of La0.7Ca0.3−xSrxMnO3 thin films by sol–gel method
8. Screening and optimization of phage display cyclic peptides against the WDR5 WBM site
9. Discovery of 1H‑Imidazo[4,5‑b]pyridine Derivatives as Potent and Selective BET Inhibitors for the Management of Neuropathic Pain.
10. Structure-Based Discovery of a Series of NSD2-PWWP1 Inhibitors
11. Structure-based Discovery of a Series of NSD2-PWWP1 Inhibitors
12. Structure-Based Discovery of Potent CARM1 Inhibitors for Solid Tumor and Cancer Immunology Therapy
13. Structure-based Discovery of a Series of NSD2-PWWP1 Inhibitor
14. Multi-Water Bridges Enable Design of BET BD1-Selective Inhibitors for Pancreatic Cancer Therapy
15. Screening and optimization of phage display cyclic peptides against the WDR5 WBM siteElectronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3md00288h
16. Phage-Display Based Discovery and Characterization of Peptide Ligands against WDR5
17. Rational Design and Evaluation of 6-(Pyrimidin-2-ylamino)-3,4-dihydroquinoxalin-2(1H)-ones as Polypharmacological Inhibitors of BET and Kinases
18. Structure-Based Discovery and Development of a Series of Potent and Selective Bromodomain and Extra-Terminal Protein Inhibitors
19. Design and Synthesis of Potent, Selective Inhibitors of Protein Arginine Methyltransferase 4 against Acute Myeloid Leukemia
20. Identification of a new series of potent diphenol HSP90 inhibitors by fragment merging and structure-based optimization
21. Structure-Based Rational Design and Evaluation of BET-Aurora Kinase Dual-Inhibitors for Treatment of Cancers
22. Annealing Effect on the Physical Properties of La0.7Sr0.3MnO3Thin Films Grown on Si Substrates Prepared by Chemical Solution Deposition Method
23. Aqueous-phase reforming of the low-boiling fraction of bio-oil for hydrogen production: The size effect of Pt/Al2O3
24. Structure, magnetic and transport properties of La0.7Ca0.3−Sr MnO3 thin films by sol–gel method
25. Highly orientated growth and characterization of La0.7Sr0.3MnO3 thin films with different orientations on SrTiO3 substrates by chemical solution deposition method
26. Fragment-Based Drug Discovery of 2-Thiazolidinones as BRD4 Inhibitors: 2. Structure-Based Optimization
27. Multi-substituted 8-aminoimidazo[1,2-a]pyrazines by Groebke–Blackburn–Bienaymé reaction and their Hsp90 inhibitory activity
28. Fragment-Based Drug Discovery of 2-Thiazolidinones as Inhibitors of the Histone Reader BRD4 Bromodomain
29. Annealing Effect on the Physical Properties of La 0.7 Sr 0.3 MnO 3 Thin Films Grown on Si Substrates Prepared by Chemical Solution Deposition Method.
30. Fragment-Based Drug Discoveryof 2-Thiazolidinonesas BRD4 Inhibitors: 2. Structure-Based Optimization.
31. Design of Selective BRD4 Inhibitors for the Treatment of Autosomal Dominant Polycystic Kidney Disease.
32. Discovery of 1 H -Imidazo[4,5- b ]pyridine Derivatives as Potent and Selective BET Inhibitors for the Management of Neuropathic Pain.
33. Rational Design and Evaluation of 6-(Pyrimidin-2-ylamino)-3,4-dihydroquinoxalin-2(1 H )-ones as Polypharmacological Inhibitors of BET and Kinases.
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