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3. Optimization of physicochemical properties of pyrrolidine GPR40 AgoPAMs results in a differentiated profile with improved pharmacokinetics and reduced off-target activities

6. Discovery of novel pyridinones as MGAT2 inhibitors for the treatment of metabolic disorders

7. Structure–activity relationship study of central pyridine-derived TYK2 JH2 inhibitors: Optimization of the PK profile through C4′ and C6 variations

10. Tricyclic sulfones as potent, selective and efficacious RORγt inverse agonists – Exploring C6 and C8 SAR using late-stage functionalization

11. Discovery of BMS-753426: A Potent Orally Bioavailable Antagonist of CC Chemokine Receptor 2

12. Azatricyclic Inverse Agonists of RORγt That Demonstrate Efficacy in Models of Rheumatoid Arthritis and Psoriasis

13. Studying rat brain neurochemistry using nanoprobe NMR spectroscopy: a metabonomics approach

15. Solution structure and phosphopeptide binding to the N-terminal domain of Yersinia YopH: comparison with a crystal structure

16. Tricyclic-Carbocyclic RORγt Inverse Agonists—Discovery of BMS-986313

18. Novel Tricyclic Pyroglutamide Derivatives as Potent RORγt Inverse Agonists Identified using a Virtual Screening Approach

19. Discovery of BMS-986251: A Clinically Viable, Potent, and Selective RORγt Inverse Agonist

23. Contributory presentations/posters

24. One-Step Diastereoselective Pyrrolidine Synthesis Using a Sulfinamide Annulating Reagent

25. Rationally Designed, Conformationally Constrained Inverse Agonists of RORγt—Identification of a Potent, Selective Series with Biologic-Like in Vivo Efficacy

29. Use of a Conformational-Switching Mechanism to Modulate Exposed Polarity: Discovery of CCR2 Antagonist BMS-741672

36. Contributory presentations/posters

37. Ni/Photoredox-Catalyzed C(sp 2 )-C(sp 3 ) Cross-Coupling of Alkyl Pinacolboronates and (Hetero)Aryl Bromides.

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