246 results on '"Che, Jinxin"'
Search Results
2. A Microenvironment-responsive small-molecule probe and application in quick acute myocardial infarction imaging
3. Integration of covalent organic frameworks and molecularly imprinted polymers for selective extraction of flavonoid naringenin from grapefruit (Citrus × paradisi Macf.) peels
4. Discovery of novel, potent, selective and orally bioavailable HPK1 inhibitor for enhancing the efficacy of anti-PD-L1 antibody
5. Promoting anti-tumor immunity by targeting TMUB1 to modulate PD-L1 polyubiquitination and glycosylation
6. Recent progress and applications of small molecule inhibitors of Keap1–Nrf2 axis for neurodegenerative diseases
7. Discovery of a potent and selective PARP1 degrader promoting cell cycle arrest via intercepting CDC25C-CDK1 axis for treating triple-negative breast cancer
8. Structure-based identification of new orally bioavailable BRD9-PROTACs for treating acute myelocytic leukemia
9. Targeted delivery of cathepsin-activatable near-infrared fluorescence probe for ultrahigh specific imaging of peritoneal metastasis
10. Advances of targeting the YAP/TAZ-TEAD complex in the hippo pathway for the treatment of cancers
11. Discovery of new macrophage M2 polarization modulators as multiple sclerosis treatment agents that enable the inflammation microenvironment remodeling
12. Altered pathways and targeted therapy in double hit lymphoma
13. Nitrogen and sulfur co-doped carbon dots derived from granatums and ammonium persulfate to detect tetracyclines in milk
14. Log P analyzation-based discovery of GSH activated biotin-tagged fluorescence probe for selective colorectal cancer imaging
15. Structure-based rational design enables efficient discovery of a new selective and potent AKT PROTAC degrader
16. Design, synthesis and biological evaluation of new dihydropyridine derivatives as PD-L1 degraders for enhancing antitumor immunity
17. Molecular dynamics insights into the selectivity toward CXCR1 and CXCR2 antagonists
18. Design, synthesis and biological evaluation of sulfonamides inhibitors of XPO1 displaying activity against multiple myeloma cells
19. Design, synthesis, and biological evaluation of quinazoline derivatives with covalent reversible warheads as potential FGFR4 inhibitors
20. Discovery of seneciobipyrrolidine derivatives for the amelioration of glucose homeostasis disorders through 4E-BP1/Akt/AMPK signaling activation
21. Fabrication of γ-cyclodextrin-Based metal-organic frameworks as a carrier of cinnamaldehyde and its application in fresh-cut cantaloupes
22. Discovery of New Phenyltetrazolium Derivatives as Ferroptosis Inhibitors for Treating Ischemic Stroke: An Example Development from Free Radical Scavengers.
23. Discovery of a Highly Potent and Selective BRD9 PROTAC Degrader Based on E3 Binder Investigation for the Treatment of Hematological Tumors.
24. Design, synthesis and biological evaluation of quinazoline derivatives as potent and selective FGFR4 inhibitors
25. Discovery of phenyl-linked symmetric small molecules as inhibitors of the programmed cell death-1/programmed cell death-ligand 1 interaction
26. Discovery of N-(1-(6-Oxo-1,6-dihydropyrimidine)-pyrazole) Acetamide Derivatives as Novel Noncovalent DprE1 Inhibitors against Mycobacterium tuberculosis
27. A Microenvironment-responsive small-molecule probe and application in quick acute myocardial infarction imaging
28. Inhibiting ferroptosis: A novel approach for stroke therapeutics
29. Development of differentiation modulators and targeted agents for treating neuroblastoma
30. Structure-based design, synthesis and bioactivity evaluation of macrocyclic inhibitors of mutant isocitrate dehydrogenase 2 (IDH2) displaying activity in acute myeloid leukemia cells
31. Rational Identification of Novel Antibody‐Drug Conjugate with High Bystander Killing Effect against Heterogeneous Tumors.
32. Targeting CXCR1/2: The medicinal potential as cancer immunotherapy agents, antagonists research highlights and challenges ahead
33. Recent progress and applications of small molecule inhibitors of Keap1–Nrf2 axis for neurodegenerative diseases
34. Discovery of a potent and selective PARP1 degrader promoting cell cycle arrest via intercepting CDC25C-CDK1 axis for treating triple-negative breast cancer
35. ADCdb: the database of antibody–drug conjugates
36. Discovery of Novel Oxazepine Derivatives as Akt/ROCK Inhibitors for Growth Arrest and Differentiation Induction in Neuroblastoma Treatment
37. An updated patent review of AKT inhibitors (2020 – present)
38. Discovery of pyrazole-thiophene derivatives as highly Potent, orally active Akt inhibitors
39. Discovery of novel indoleaminopyrimidine NIK inhibitors based on molecular docking-based support vector regression (SVR) model
40. ADCdb: the database of antibody–drug conjugates.
41. TransFoxMol: predicting molecular property with focused attention
42. ClusterX: a novel representation learning-based deep clustering framework for accurate visual inspection in virtual screening
43. AKT inhibitor Hu7691 induces differentiation of neuroblastoma cells
44. Genomic sequencing, genome-scale metabolic network reconstruction, and in silico flux analysis of the grape endophytic fungus Alternaria sp. MG1
45. Screening of Oxygenated Aromatic Compounds for Potential Antifungal Activity against Geotrichum citri-aurantii through Structure–Activity Relationship Analysis
46. Structural Feature Analyzation Strategies toward Discovery of Orally Bioavailable PROTACs of Bruton’s Tyrosine Kinase for the Treatment of Lymphoma
47. Integrating docking scores, interaction profiles and molecular descriptors to improve the accuracy of molecular docking: Toward the discovery of novel Akt1 inhibitors
48. Identification of Novel Covalent XPO1 Inhibitors Based on a Hybrid Virtual Screening Strategy
49. Production of pinoresinol diglucoside, pinoresinol monoglucoside, and pinoresinol by Phomopsis sp. XP-8 using mung bean and its major components
50. Structure-Based Rational Design Enables Discovery of a New Selective and Potent Akt Degrader with Improved Dermatologic Safety
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.