24 results on '"Kaldor, Stephen"'
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2. Discovery of KIN-3248, An Irreversible, Next Generation FGFR Inhibitor for the Treatment of Advanced Tumors Harboring FGFR2 and/or FGFR3 Gene Alterations.
3. Azetidinones as vasopressin V1a antagonists
4. Discovery of CC-90011: A Potent and Selective Reversible Inhibitor of Lysine Specific Demethylase 1 (LSD1).
5. A Convenient, Large Scale Synthesis of N-CBZ-(S-Phenyl)-L-Cysteine.
6. 5-HT1F receptor agonists inhibit neurogenic dural inflammation in guinea pigs.
7. ChemInform Abstract: Expedited Discovery of Second Generation NK-1 Antagonists: Identification of a Nonbasic Aryloxy Substituent.
8. ChemInform Abstract: The Synthesis of Ethanolamine Libraries from Olefin Scaffolds.
9. New dipeptide isosteres useful for the inhibition of HIV-1 protease
10. Discovery of antirhinoviral leads by screening a combinatorial library of ureas prepared using covalent scavengers
11. ITERATIVE PROTEIN STRUCTURE-BASED DRUG DESIGN AND SYNTHESIS OF HIV PROTEASE INHIBITORS
12. Rapid purification of small molecule libraries by ion exchange chromatography
13. Use of solid supported nucleophiles and electrophiles for the purification of non-peptide small molecule libraries
14. Solid phase synthesis of hydantoins using a carbamate linker and a novel cyclization / cleavage step
15. Synthesis of 2′,3′-dideoxy-3′-hydroxymethylcytidine; a unique antiviral nucleoside
16. Isophthalic acid derivatives: amino acid surrogates for the inhibition of HIV-1 protease
17. Structure-based drug design of nonpeptidic P 2 substituents for HIV-1 protease inhibitors
18. A systematic study of P 1–P 3 spanning sidechains for the inhibition of HIV-1 protease
19. Glutamine-derived aldehydes for the inhibition of human rhinovirus 3C protease
20. Combinatorial chemistry using polymer-supported reagents
21. Solid phase synthesis of urea libraries using a diversifiable thiophenoxy carbonyl linker
22. Synthesis of 2′,3′-dideoxy-3′-hydroxymethylcytidine: A novel hydroformylation route
23. Design, synthesis and biological evaluation of novel 4-phenylisoquinolinone BET bromodomain inhibitors.
24. Discovery of TAK-960: An orally available small molecule inhibitor of polo-like kinase 1 (PLK1).
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