Font Size: a A A
Keyword [design synthesis]
Result: 41 - 60 | Page: 3 of 10
41. Study On Design Synthesis And Antitumor Activity Of CA - 4 Analogues
42. Study On The Design, Synthesis And Structure - Activity Relationship Of β - Secretase Inhibitors
43. Study On The Relationship Between The Design, Synthesis And Anti - Tuberculosis - Structure Of Imidazole [1,2 - A] Pyridine - 3 - Amide Compounds
44. NO-donating Genistein Prodrug: Design, Synthesis And It's Bioactivities On Osteoblast
45. Design, Synthesis And Antitumor Activities Study Of 1,2,4-Benzotriazine-1,4-dioxide And Analogues
46. Design, Synthesis And SAR Study Of Arylmaleimide Derivatives As Anti-tumor Compounds
47. Design, Synthesis And Biological Activity Study Of New Sinapyl Alcohol Derivaties, Neolignans And Its Nitrogen-containing Analogues
48. Design, Synthesis And SAR Study Of Analogues Of Combretastatin A-4 As Anti-tumor Agents
49. Design, Synthesis And Bioactivity Investigation Of Oleanolic Acid Derivatives
50. Design, Synthesis And Activity Evaluation Of Novel Melanotropin Analogues
51. Design, Synthesis And Evaluation Of BACE1 Inhibitors For The Treatment Of Alzheimer's Disease
52. Design, Synthesis And Activity Evaluation Of α-Halogen Substituted Succinate-Based Hydroxamic Acids As Matrix Metalloproteases Inhibitors
53. Structure-Based Design, Synthesis And Screening Of CCR5 Antagonists As HIV-1 Entry Inhibitors
54. Modification Of Endomorphin-1 To Enhance The Blood-brain Barrier Permeability: Design, Synthesis And Biological Activity Characterization
55. Design, Synthesis And Preliminary Activity Assay Of Influenza Virus Neuraminidase Inhibitors
56. Design, Synthesis And Preliminary Evaluation Of Matrix Metalloproteinase-2 Inhibitors Based On Pyrrolidine Scaffold
57. Design, Synthesis And Neuroprotective Activity Assay Of Carnitine Esters As Prodrug
58. Design, Synthesis And Biological Evaluation Of Indole And Tetrahydroisoquinoline Derivatives
59. Design, Synthesis And Bioactivity Of Novel 3-Arylazepanes For μ And δ Opioid Receptors
60. Molecular Design, Synthesis And SAR Research Of 2,5,6-trisubstituted S-DABO And 6-naphthylmethyl Substituted N-DABO Analogues As Nonnucleoside HIV-1 Reverse Transcriptase Inhibitors
  <<First  <Prev  Next>  Last>>  Jump to