387 results on '"Jiang, Xianxing"'
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2. Design and discovery of a highly potent ultralong-acting GLP-1 and glucagon co-agonist for attenuating renal fibrosis
3. Discovery of Novel Peptide Antagonists Targeting GPR55 for Liver Inflammation and Fibrosis.
4. Design and Synthesis of Novel Ultralong-Acting Peptides as EDP-EBP Interaction Inhibitors for Pulmonary Fibrosis Treatment.
5. Author Correction: AdipoR1/AdipoR2 dual agonist recovers nonalcoholic steatohepatitis and related fibrosis via endoplasmic reticulum-mitochondria axis
6. Catalytic asymmetric nucleophilic fluorination using BF3·Et2O as fluorine source and activating reagent
7. RAP-8 ameliorates liver fibrosis by modulating cell cycle and oxidative stress
8. Harnessing the Lysosomal Sorting Signals of the Cation-Independent Mannose-6-Phosphate Receptor for Targeted Degradation of Membrane Proteins
9. Potent effects of amino acid scanned antimicrobial peptide Feleucin-K3 analogs against both multidrug-resistant strains and biofilms of Pseudomonas aeruginosa
10. AdipoR1/AdipoR2 dual agonist recovers nonalcoholic steatohepatitis and related fibrosis via endoplasmic reticulum-mitochondria axis
11. Discovery and Design of Novel Cyclic Peptides as Specific Inhibitors Targeting CCN2 and Disrupting CCN2/EGFR Interaction for Kidney Fibrosis Treatment
12. Design and Discovery of Novel Cyclic Peptides as EDPs–EBP Interaction Inhibitors for the Treatment of Liver Fibrosis
13. Different Performances of BF3, BCl3, and BBr3 in Hypervalent Iodine-Catalyzed Halogenations
14. Synergistic activation of AMPK by AdipoR1/2 agonist and inhibitor of EDPs–EBP interaction recover NAFLD through enhancing mitochondrial function in mice
15. Structure-Guided Design of Halofuginone Derivatives as ATP-Aided Inhibitors Against Bacterial Prolyl-tRNA Synthetase
16. Halogenation of Unsaturated Amides: Synthesis of Halogenated (Spiro)Oxazolines
17. Novel antimicrobial peptide CPF‐C1 analogs with superior stabilities and activities against multidrug‐resistant bacteria
18. Different Performances of BF3, BCl3, and BBr3 in Hypervalent Iodine-Catalyzed Halogenations.
19. Design of a highly potent GLP-1R and GCGR dual-agonist for recovering hepatic fibrosis
20. 173 DUAL ACTIVATION OF GCGR/GLP1R SIGNALING AMELIORATES INTESTINAL FIBROSIS VIA METABOLIC REGULATION OF HISTONE H3K9 LACTYLATION IN EPITHELIAL CELLS
21. Development, validation and application of a UHPLC–MS/MS method for quantification of the adiponectin‐derived active peptide ADP355 in rat plasma
22. Design and discovery of a highly potent ultralong-acting GLP-1 and glucagon co-agonist for attenuating renal fibrosis by modulating mitochondrial function
23. Lewis Acid-Mediated Efficient Synthesis of 4H-1,3-benzo-xazines and Their Derivatives 4,5-dihydro-1,3-benzo-xazepines
24. Different Performances of BF3, BCl3, and BBr3in Hypervalent Iodine-Catalyzed Halogenations
25. Synthesis of diphosphite ligands derived from glucopyranoside and their application in the Cu-catalyzed asymmetric 1,4-addition of organozinc to enones
26. Design and synthesis of a tridentate ligand inspired by the phenomenon of self-assembly catalysis and its application in the asymmetric alkynylation of N-(diphenylphosphinoyl) imines
27. Dual Blockade of Lactate/GPR81 and PD-1/PD-L1 Pathways Enhances the Anti-Tumor Effects of Metformin
28. Visible‐Light‐Driven Redox Neutral Direct C−H Amination of Glycine Derivatives and Peptides with N ‐Acyloxyphthalimides
29. A CDR-based approach to generate covalent inhibitory antibody for human rhinovirus protease
30. Development of a Broadly Applicable Cas12a-Linked Beam Unlocking Reaction for Sensitive and Specific Detection of Respiratory Pathogens Including SARS-CoV-2
31. The antimicrobial peptide YD attenuates inflammation via miR-155 targeting CASP12 during liver fibrosis
32. Suzuki Cross‐Coupling Reaction with Genetically Encoded Fluorosulfates for Fluorogenic Protein Labeling
33. Metal-free fluoroalkylfluoroalkylselenolation of unactivated alkenes: incorporation of two photoinduced processes
34. Protein labeling approach to improve lysosomal targeting and efficacy of antibody–drug conjugates
35. Rhodium-Catalyzed Formal C–O Insertion in Carbene/Alkyne Metathesis Reactions: Synthesis of 3-Substituted 3H-Indol-3-ols
36. Trapping of Zwitterionic Intermediates by Isatins and Imines: Synthesis of Benzoxazines Bearing a C4-Quaternary Stereocenter
37. Photoactivatable Fluorogenic Labeling via Turn‐On “Click‐Like” Nitroso‐Diene Bioorthogonal Reaction
38. Triphenylphosphine‐Catalyzed Diastereoselective Addition of Oxazolones to Isatin‐Derived Ketimines: Construction of Vicinal N‐Substituted Quaternary Stereocenters
39. Nucleophilic construction of sulfate bonds: simplified access to polysulfates and polysulfonates
40. Site-specific labeling of an anti-MUC1 antibody: probing the effects of conjugation and linker chemistry on the internalization process
41. Highly efficient regio-selective ring-opening nucleophilic fluorination of aziridines and azetidines: access to β- or γ-fluorinated amino acid derivatives
42. Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocentersviaasymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
43. Rapeseed Protein-Derived Antioxidant Peptide RAP Ameliorates Nonalcoholic Steatohepatitis and Related Metabolic Disorders in Mice
44. Synthesis of Benzofused N-Heterocycles via Rh(III)-Catalyzed Direct Benzannulation with 1,3-Dienes
45. Catalytic Asymmetric [4 + 3] Annulation of C,N-Cyclic Azomethine Imines with Copper Allenylidenes
46. Rapeseed Protein-Derived Antioxidant Peptide RAP Ameliorates Nonalcoholic Steatohepatitis and Related Metabolic Disorders in Mice
47. Discovery and Design of Novel Cyclic Peptides as Specific Inhibitors Targeting CCN2 and Disrupting CCN2/EGFR Interaction for Kidney Fibrosis Treatment
48. Phosphine-Catalyzed Enantioselective [4 + 2] Cycloaddition–Semipinacol-Type-Rearrangement Reaction of Morita–Baylis–Hillman Carbonates
49. Asymmetric Synthesis of Bispiro[γ-butyrolactone-pyrrolidin-4,4′-pyrazolone] Scaffolds Containing Two Quaternary Spirocenters via an Organocatalytic 1,3-Dipolar Cycloaddition
50. Highly diastereoselective oxa-[3+3] cyclization with C,N-cyclic azomethine imines via the copper-catalyzed aerobic oxygenated CC bond of indoles
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