40 results on '"Jaxa-Chamiec Albert"'
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2. Cancer-selective targeting of the NF-?B survival pathway with GADD45ß/MKK7 inhibitors
3. Cancer-Selective Targeting of the NF-kappa B Survival Pathway with GADD45 beta/MKK7 Inhibitors
4. Peptide inhibitors of Gadd45b interaction with MKK7 kinase and their use in treatment of cancer, inflammation and other diseases
5. Cancer-Selective Targeting of the NF-κB Survival Pathway with GADD45β/MKK7 Inhibitors
6. Gadd45beta targeting agents
7. Enantioselective synthesis of 3,6-dihydro-1H-pyridin-2-ones: unexpected regioselectivity in the palladium-catalysed decarboxylative carbonylation of 5-vinyloxazolidin-2-ones
8. Prospective use of molecular field points in ligand-based virtual screening: efficient identification of new reversible Cdc25 inhibitors
9. Structural and Functional Analyses of the Second-Generation Integrase Strand Transfer Inhibitor Dolutegravir (S/GSK1349572)
10. Discovery of 1-(3-{2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)-2-imidazolidinone (GSK163090), a Potent, Selective, and Orally Active 5-HT1A/B/D Receptor Antagonist
11. ChemInform Abstract: Enantioselective Synthesis of 3,6-Dihydro-1H-pyridin-2-ones: Unexpected Regioselectivity in the Palladium-Catalyzed Decarboxylative Carbonylation of 5-Vinyloxazolidin-2-ones.
12. Diaryl substituted pyrrolidinones and pyrrolones as 5-HT2C inhibitors: Synthesis and biological evaluation
13. Diaryl substituted pyrrolidinones and pyrrolones as 5-HT 2C inhibitors: Synthesis and biological evaluation
14. A GAL4-based yeast three-hybrid system for the identification of small molecule–target protein interactions
15. ChemInform Abstract: An Approach to the Synthesis of 5,5‐trans‐Fused Lactam Analogues of β‐Lactam Antibiotics.
16. The synthesis of cyclic tetrapeptoid analogues of the antiprotozoal natural product apicidin
17. An approach to the synthesis of 5,5-trans-fused lactam analogues of β-lactam antibiotics
18. SK&F 97426-A: A Novel Bile Acid Sequestrant with Higher Affinities and Slower Dissociation Rates for Bile Acids in vitro Than Cholestyramine
19. Vitamin D 3 synthetic studies. Intramolecular Diels-Alder approaches to the CD-ring fragment
20. Synthesis of cyclopentylamines using zirconium chemistry
21. Convergent Synthesis of Aminobicyclo[3.3.0]octenes Using Zirconium Chemistry An Unusual Anti-1,3-Amine Shift.
22. Formation of zirconocene η2-imine complexes by rearrangement of cyclic iminoacyl complexes.
23. Discovery of 1-(3-{2-[4-(2-Methyl-5-quinolinyl)-1-piperazinyl]ethyl}phenyl)-2-imidazolidinone (GSK163090), a Potent, Selective, and Orally Active 5-HT1A/B/D Receptor Antagonist.
24. 1-Azadiene complexes of zirconocene
25. On the preparation and rearrangement of some vinylic sulphoxides
26. Octimibate, a potent non-prostanoid inhibitor of platelet aggregation, acts via the prostacyclin receptor
27. Novel Thymidine Analogues via Reaction of Unprotected 5'-Deoxy-5'-iodothymidine with Dianions
28. Preparation and properties of substituted 6β-vinylpenicillanic acids.
29. A new route to 5-substituted resorcinols and related systems.
30. SK&F 97426-A: A novel bile acid sequestrant with higher affinities and slower dissociation rates for bile acids <TOGGLE>in vitro</TOGGLE> than cholestyramine
31. Vitamin D3synthetic studies. Intramolecular Diels-Alder approaches to the CD-ring fragment
32. SK&F 97426-A: A Novel Bile Acid Sequestrant with Higher Affinities and Slower Dissociation Rates for Bile Acids in vitroThan Cholestyramine
33. Preparation and rearrangement of some conjugated phenylsulphinylacetate derivatives.
34. A new β-lactam expansion reaction of a spiropenicillanic acid
35. Aromatic acylation/reduction: an efficient Friedel–Crafts alkylation reaction
36. A new route to 5-substituted resorcinols
37. ChemInform Abstract: Enantioselective Synthesis of 3,6-Dihydro-1H-pyridin-2-ones: Unexpected Regioselectivity in the Palladium-Catalyzed Decarboxylative Carbonylation of 5-Vinyloxazolidin-2-ones.
38. Formation of zirconocene η 2-imine complexes by rearrangement of cyclic iminoacyl complexes.
39. Vitamin D3 synthetic studies. Intramolecular Diels-Alder approaches to the CD-ring fragment
40. Diaryl substituted pyrrolidinones and pyrrolones as 5-HT2C inhibitors: Synthesis and biological evaluation
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