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2. Making Protein Degradation Visible: Discovery of Theranostic PROTACs for Detecting and Degrading NAMPT

4. Strategies for designing proteolysis targeting chimaeras (PROTACs)

5. Procoxacin bidirectionally inhibits osteoblastic and osteoclastic activity in bone and suppresses bone metastasis of prostate cancer

6. Discovery of Highly Potent Nicotinamide Phosphoribosyltransferase Degraders for Efficient Treatment of Ovarian Cancer

7. Blocking Non-enzymatic Functions by PROTAC-Mediated Targeted Protein Degradation

8. Aptamer‐PROTAC Conjugates (APCs) for Tumor‐Specific Targeting in Breast Cancer

9. Molecular Glues for Targeted Protein Degradation: From Serendipity to Rational Discovery

10. Synthesis and evaluation of new sesamol-based phenolic acid derivatives with hypolipidemic, antioxidant, and hepatoprotective effects

11. MASM inhibits cancer stem cell-like characteristics of EpCAM

12. Nucleic-Acid-Based Targeted Degradation in Drug Discovery

13. Visible-light-driven cascade radical cyclization toward the synthesis of α-carbonyl alkyl-substituted benzimidazo[2,1-a]isoquinolin-6(5H)-one derivatives

15. Homo-PROTAC mediated suicide of MDM2 to treat non-small cell lung cancer

16. Potent Dual BET/HDAC Inhibitors for Efficient Treatment of Pancreatic Cancer

17. Optimization of clofibrate with O-desmethyl anetholtrithione lead to a novel hypolipidemia compound with hepatoprotective effect

18. Targeted delivery of a PROTAC induced PDEδ degrader by a biomimetic drug delivery system for enhanced cytotoxicity against pancreatic cancer cells

19. Molecular Engineering of Polymyxin B for Imaging and Treatment of Bacterial Infections

20. Hydrophobic Tagging-Induced Degradation of PDEδ in Colon Cancer Cells

21. Hydrocarbon stapling modification of peptide alyteserin-2a: Discovery of novel stapled peptide antitumor agents

22. Development of novel bone targeting peptide-drug conjugate of 13-aminomethyl-15-thiomatrine for osteoporosis therapy

24. Visible-Light-Driven Sulfonylation/Cyclization to Access Sulfonylated Benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-ones

25. Efficient synthesis of artificial pharmaceutical solid-phase modules for constructing aptamer-drug conjugates

26. A novel BRD4 inhibitor suppresses osteoclastogenesis and ovariectomized osteoporosis by blocking RANKL-mediated MAPK and NF-κB pathways

27. Design, Synthesis, and Antitumor Activities Study of Stapled A4K14-Citropin 1.1 Peptides

30. Small Molecules Simultaneously Inhibiting p53-Murine Double Minute 2 (MDM2) Interaction and Histone Deacetylases (HDACs): Discovery of Novel Multitargeting Antitumor Agents

31. Discovery of Novel Indoleamine 2,3-Dioxygenase 1 (IDO1) and Histone Deacetylase (HDAC) Dual Inhibitors

32. Structural simplification and bioisostere principle lead to Bis-benzodioxole-fibrate derivatives as potential hypolipidemic and hepatoprotective agents

33. Irrigation amount dominates soil mineral nitrogen leaching in plastic shed vegetable production systems

36. Improving the Potency of Cancer Immunotherapy by Dual Targeting of IDO1 and DNA

37. Design, synthesis and biological evaluation of novel antitumor spirotetrahydrothiopyran–oxindole derivatives as potent p53-MDM2 inhibitors

38. Design, synthesis and biological evaluation of novel antitumor spirodihydrothiopyran-oxindole derivatives

39. Synthesis of spiro-tetrahydrothiopyran-oxindoles by Michael-aldol cascade reactions: discovery of potential P53-MDM2 inhibitors with good antitumor activity

40. Design of waveguide to microstrip directional coupler with rectangular apertures as fishbone shape for high power applications

41. Identification of benzothiophene amides as potent inhibitors of human nicotinamide phosphoribosyltransferase

42. Discovery of Novel Multiacting Topoisomerase I/II and Histone Deacetylase Inhibitors

43. Scaffold hopping of sampangine: discovery of potent antifungal lead compound against Aspergillus fumigatus and Cryptococcus neoformans

44. Study of binding glycyrrhetic acid to AT1 receptor

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