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Keyword [pyrazole]
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1. Study On Design Synthesis And Antitumor Activity Of CA - 4 Analogues
2. Effects Of Three Inducers On CYP2E1 Expression And Liver - Related Enzymes In Rats
3. Design, Synthesis And Anti-inflammatory Activity Of Pyrazole Class Of COX-2 Selective Inhibitors
4. Studies On The Design, Synthesis Of CB1 Receptor Antagonists
5. Study On The Relationship Between Structures And Properties Of Five Serie Drug Compounds And Liquid Crystals Containing A Fluoro-Group
6. Synthesis And Bioactivity Evaluation Of Novel Pyrazole Derivatives
7. Effects Of New Pyrazole Derivatives On Apoptosis Of Vascular Endothelial Cells And A549 Lung Cancer Cells And The Corresponding Mechanisms
8. Synthesis Of Heterocycles With Pyridazinone Skeleton Structure
9. Design, Synthesis And Biological Evaluation Of NO Donor Selective COX-2 Inhibitor
10. Design, Synthesis, Structure And Biological Evaluation Of Ferrocenyl Prazole-fused Heterocyclone Compounds
11. Design, Synthesis And SAR Study Of Nitrogen-contained Chalcone Derivatives As CDK1 Inhibitors
12. The Affection Of NAFLD And Pyrazole, Phenobaebital To CYP2A5 Expression
13. Study On Synthesis And Anti-asthmatic Activity Of 8-nitro Benzyl Pyrazol Substituted Xanthine
14. Sildenafil Intermediate 1 - Methyl - 3 - N-propyl -4 - Nitro-pyrazole-5 - Carboxamide,
15. .2,6 - Two Pyrazole Pyridine Ruthenium (ii) Complexes Of Rucl <sub> 2 </ Sub> (pph <sub> 3 </ Sub>) (me, <sub> 4 </ Sub> Bppy) Catalytic Ketone Hydrogen Transfer And Hydrogenation Reaction
16. .5,6 - Dihydro - (9h) - Pyrazole [3,4-c] - 1, 2,4 - Triazolo [4,3-a] Pyridine Inhibitor And Quantitative Structure Of The Hsv-1 Inhibitors Effect Relationship
17. Fxr Antagonist Design, Synthesis And Pharmacological Activities Of 4 - Methyl Substituted Pyrazole Research And Study On The Method Of Flavone Derivatives
18. Design,Synthesis And Biological Evaluation Of P53-MDM2Binding Inhibitors
19. Method Of Shu, For The Protection And Pyrazole Of Pulmonary Fibrosis Ketone Side Effects For The Treatment Of Pulmonary Fibrosis
20. Studies On The Synthesis And In Vitro Antitumor Activities Of Novel D-ring Modified Isosteviol-heterocycle Derivatives
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