28 results on '"Qu, Shuhao"'
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2. Design, synthesis, antibacterial/antitumor activity and in vitro stability of novel cordycepin derivatives with unsaturated fatty acid chain
3. Correction to “Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity”
4. Phosphorylation Modification, Structural Characterization, Antioxidant and DNA Protection Capacities of Polysaccharides from Asarum SieboldiiMiq
5. Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity
6. Antioxidant and DNA protecting activity of carboxymethylated polysaccharides from Cortex periplocae
7. Design, synthesis, and anticancer activity of C8-substituted-4′-thionucleosides as potential HSP90 inhibitors
8. Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity.
9. Study on 'shi' as a Demonstrative Pronoun in Modern Chinese
10. Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity
11. Novel 2,3-dihydro-1H-imidazo[2,1-a]isoquinolin-4-ium salts: synthesis, antitumor and antibacterial activity
12. Design, Synthesis and Insecticidal Activity of 3-Arylisoxazoline-N-alkylpyrazole-5-carboxamide Derivatives against Tetranychus urticae Koch
13. Design, Synthesis, and Anti-RNA Virus Activity of 6′-Fluorinated-Aristeromycin Analogues
14. Design, Synthesis, and Anti-RNA Virus Activity of 6′-Fluorinated-Aristeromycin Analogues.
15. Correction to "Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity".
16. Asymmetric Synthesis of (−)-6′-β-Fluoro-aristeromycin via Stereoselective Electrophilic Fluorination
17. Structure-Activity Relationships of Acyclic Selenopurine Nucleosides as Antiviral Agents
18. Asymmetric Synthesis of (−)-6′-β-Fluoro-aristeromycin via Stereoselective Electrophilic Fluorination
19. Correction to “Structure–Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A2A/A3Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity”
20. ChemInform Abstract: Synthesis and anti-HIV Activity of 5′-Homo-2′,3′-dideoxy-2′,3′-didehydro-4′-selenonucleosides (5′-Homo-4′-Se-d4 Ns).
21. Synthesis and Anti-HIV Activity of 5′-Homo-2′,3′-dideoxy-2′,3′-didehydro-4′-selenonucleosides (5′-Homo-4′-Se-d4 Ns)
22. Stereo- and regio-selective synthesis of 3′-C-substituted-(N)-methanocarba adenosines as potential anticancer agents
23. Stereoselective Synthesis of d-5-Homo-4-selenoribose as a Versatile Intermediate for 4′-Selenonucleosides
24. Design, synthesis and cellular metabolism study of 4′-selenonucleosides
25. Study on ˵shi″ as a Demonstrative Pronoun in Modern Chinese.
26. Correction to "Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A 2A /A 3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity".
27. Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A 2A /A 3 Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity.
28. Asymmetric Synthesis of (-)-6'-β-Fluoro-aristeromycin via Stereoselective Electrophilic Fluorination.
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