27 results on '"Barr, Kenneth J."'
Search Results
2. Structure-Based Design and Identification of FT-2102 (Olutasidenib), a Potent Mutant-Selective IDH1 Inhibitor
3. Applications of vinylogous Mannich reactions. Concise enantiospecific total syntheses of (+)-croomine
4. Titanocene-catalyzed reduction of esters using polymethylhydrosiloxane as the stoichiometric reductant
5. Discovery and Optimization of Quinolinone Derivatives as Potent, Selective, and Orally Bioavailable Mutant Isocitrate Dehydrogenase 1 (mIDH1) Inhibitors
6. FT-1101: A Structurally Distinct Pan-BET Bromodomain Inhibitor with Activity in Preclinical Models of Hematologic Malignancies
7. Karyological and biochemical evidence for chromosomal dedifferentiation in neoplasia
8. Structure–activity relationship (SAR) of the α-amino acid residue of potent tetrahydroisoquinoline (THIQ)-derived LFA-1/ICAM-1 antagonists
9. Discovery of tetrahydroisoquinoline (THIQ) derivatives as potent and orally bioavailable LFA-1/ICAM-1 antagonists
10. Finding jobs in biopharma
11. Vinylogous Mannich reactions: the asymmetric total synthesis of (+)-croomine
12. Design and synthesis of 2-amino-pyrazolopyridines as Polo-like kinase 1 inhibitors
13. Discovery and Development of Potent LFA-1/ICAM-1 Antagonist SAR 1118 as an Ophthalmic Solution for Treating Dry Eye
14. ChemInform Abstract: Applications of Vinylogous Mannich Reactions. Concise Enantiospecific Total Syntheses of (+)-Croomine.
15. LAUNCHING A SCIENCE CAREER
16. Structure of theBrachydanio rerioPolo-like kinase 1 (Plk1) catalytic domain in complex with an extended inhibitor targeting the adaptive pocket of the enzyme
17. Allosteric inhibition of protein tyrosine phosphatase 1B
18. Potent, Orally Active Heterocycle-Based Combretastatin A-4 Analogues: Synthesis, Structure−Activity Relationship, Pharmacokinetics, and In Vivo Antitumor Activity Evaluation.
19. Synthesis and Biological Evaluation of 2-Indolyloxazolines as a New Class of Tubulin Polymerization Inhibitors. Discovery of A-289099 as an Orally Active Antitumor Agent
20. Novel sulfonate analogues of combretastatin A-4
21. Second-Generation Peptidomimetic Inhibitors of Protein Farnesyltransferase Demonstrating Improved Cellular Potency and Significant in Vivo Efficacy
22. Zirconocene(iso-butyl) chloride: In situ generation of a zirconocene(methyl) chloride equivalent for use in organic synthesis
23. Retroversion and infertility
24. ChemInform Abstract: Applications of Vinylogous Mannich Reactions. Concise Enantiospecific Total Syntheses of (+)-Croomine.
25. Zirconocene( iso-butyl) chloride: In situ generation of a zirconocene(methyl) chloride equivalent for use in organic synthesis
26. Structure of the Brachydanio rerio Polo-like kinase 1 (Plk1) catalytic domain in complex with an extended inhibitor targeting the adaptive pocket of the enzyme.
27. Potent, orally active heterocycle-based combretastatin A-4 analogues: synthesis, structure-activity relationship, pharmacokinetics, and in vivo antitumor activity evaluation.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.