336 results on '"Jiang, Cheng-Shi"'
Search Results
2. Synthesis and biological evaluation of 1-phenyl-tetrahydro-β-carboline-based first dual PRMT5/EGFR inhibitors as potential anticancer agents
3. Discovery of tetrahydroisoquinolineindole derivatives as first dual PRMT5 inhibitors/hnRNP E1 upregulators: Design, synthesis and biological evaluation
4. Further undescribed cembranoids from South China Sea soft coral Sarcophyton ehrenbergi: Structural elucidation and biological evaluation
5. Iboga-type alkaloids with Indolizidino[8,7-b]Indole scaffold and bisindole alkaloids from Tabernaemontana bufalina Lour
6. Design and semisynthesis of oleanolic acid derivatives as VEGF inhibitors: Inhibition of VEGF-induced proliferation, angiogenesis, and VEGFR2 activation in HUVECs
7. Design, synthesis and biological evaluation of marine phidianidine-inspired derivatives against oxidized ldl-induced endothelial injury by activating Nrf2 anti-oxidation pathway
8. Discovery of new 2-phenyl-1H-benzo[d]imidazole core-based potent α-glucosidase inhibitors: Synthesis, kinetic study, molecular docking, and in vivo anti-hyperglycemic evaluation
9. Novel tetrahydrobenzo[b]thiophen-2-yl)urea derivatives as novel α-glucosidase inhibitors: Synthesis, kinetics study, molecular docking, and in vivo anti-hyperglycemic evaluation
10. Discovery of 3-(1H-indol-5-yl)-1,2,4-oxidizable derivatives as non-competitive α-glucosidase inhibitors
11. A highly sensitive endoplasmic reticulum-targeting fluorescent probe for the imaging of endogenous H2S in live cells
12. Design, synthesis, and evaluation of novel ferrostatin derivatives for the prevention of HG-induced VEC ferroptosis
13. An updated research of glycogen synthase kinase-3β inhibitors: a review
14. Discovery of Novel Marine‐Derived Phidiandine/Lipoic Acid Hybrid as a Potential Anti‐atherosclerosis Agent: Design, Synthesis and in Vitro/in Vivo Evaluation
15. A New Endoplasmic Reticulum (ER)-Targeting Fluorescent Probe for the Imaging of Cysteine in Living Cells
16. Synthesis and biological evaluation of quinoline/cinnamic acid hybrids as amyloid-beta aggregation inhibitors
17. Synthesis and biological evaluation of novel 1,2,3,4-tetrahydro-β-carboline derivatives as potential antibacterial agents
18. Methyl 2-naphthoates from a traditional Chinese herb Morinda officinalis var. officinalis
19. Discovery of Novel Marine‐Derived Phidiandine/Lipoic Acid Hybrid as a Potential Anti‐Atherosclerosis Agent: Design, Synthesis and in Vitro/in Vivo Evaluation.
20. Synthesis and biological evaluation of ferrostatin-based diamide derivatives as new ferroptosis inhibitors
21. An Updated Overview of Synthetic α-glucosidase Inhibitors: Chemistry and Bioactivities
22. Antibacterial sorbicillin and diketopiperazines from the endogenous fungus Penicillium sp. GD6 associated Chinese mangrove Bruguiera gymnorrhiza
23. Discovery of new multifunctional selective acetylcholinesterase inhibitors: structure-based virtual screening and biological evaluation
24. Synthesis and biological evaluation of 2-(3-aminophenyl)-benzothiazoles as antiproliferative and apoptosis-inducing agents
25. Photodynamic Therapy treatment of onychomycosis with Aluminium-Phthalocyanine Chloride nanoemulsions: A proof of concept clinical trial
26. On a Sum of More Complex Product-Type Operators from Bloch-Type Spaces to the Weighted-Type Spaces
27. Synthesis and evaluation of coumarin/piperazine hybrids as acetylcholinesterase inhibitors
28. PRMT5 promotes ovarian cancer growth through enhancing Warburg effect by methylating ENO1
29. Arginine methyltransferase 5 (PRMT5) inhibitors with 3-(1H-benzo[d]imidazol-2-yl)anilines core identified by virtual screening and biological evaluation
30. Discovery of marine phidianidine-based Nrf2 activators and their potential against oxLDL- and HG-induced injury in HUVECs
31. Design and semisynthesis of oleanolic acid derivatives as VEGF inhibitors: Inhibition of VEGF-induced proliferation, angiogenesis, and VEGFR2 activation in HUVECs
32. Design, synthesis, and evaluation of novel ferrostatin derivatives for the prevention of HG-induced VEC ferroptosisElectronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d4md00038b
33. New cycloalkyl[b]thiophenylnicotinamide-based α-glucosidase inhibitors as promising anti-diabetic agents: Synthesis, in silico study, in vitro and in vivo evaluations
34. Synthesis and biological evaluation of benzothiazol-based 1,3,4-oxadiazole derivatives as amyloid β-targeted compounds against Alzheimer’s disease
35. Further casbane-type diterpenes from the soft coral Sinularia depressa
36. Topsendines A–F, new 3-alkylpyridine alkaloids from a Hainan sponge Topsentia sp.
37. New aspidosperma-type alkaloids from Tabernaemontana bovina
38. Recent Advances in Antimicrobial Nano-Drug Delivery Systems
39. Uncommon eunicellin-based diterpenoid and 9, 11-secosteroid from the Sanya soft coral Cladiella krempfi: Structure and stereochemistry
40. Epipolythiodioxopiperazines from Fungi: Chemistry and Bioactivities
41. Japonisine A, a fawcettimine-type Lycopodium alkaloid with an unusual skeleton from Lycopodium japonicum Thunb
42. Design, synthesis and biological evaluation of novel (E)-2-benzylidene-N-(3-cyano-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)hydrazine-1-carboxamide derivatives as α-glucosidase inhibitors
43. New Cembrane‐Type Diterpenoids from the South China Sea Soft Coral Sinularia nanolobata
44. Recent progress regarding the bioactivities, biosynthesis and synthesis of naturally occurring resorcinolic macrolides
45. Cipatrijugin G, a new trijugin-type limonoid bearing an uncommon γ-hydroxybutenolide unit from the aerial parts of Cipadessa cinerascens
46. New monoterpenoid indole alkaloids from Tabernaemontana bovina
47. Sinucrassins A—K, Casbane‐type Diterpenoids from the South China Sea Soft Coral Sinularia crassa
48. Autophagy Induced by a Novel Triazol Derivative Promotes Angiogenesis Through Decreasing Interferon-Inducible Protein 10 Level in Vascular Endothelial Cells
49. Natural products possessing protein tyrosine phosphatase 1B (PTP1B) inhibitory activity found in the last decades
50. Synthesis and evaluation of 1,2,4-oxadiazole derivatives as potential anti-inflammatory agents by inhibiting NF-κB signaling pathway in LPS-stimulated RAW 264.7 cells
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