28 results on '"Deaton, David"'
Search Results
2. Novel heterocyclic scaffolds of GW4064 as farnesoid X receptor agonists
3. Conformationally constrained farnesoid X receptor (FXR) agonists: Alternative replacements of the stilbene
4. Conformationally constrained farnesoid X receptor (FXR) agonists: Heteroaryl replacements of the naphthalene
5. Substituted isoxazole analogs of farnesoid X receptor (FXR) agonist GW4064
6. FXR agonist activity of conformationally constrained analogs of GW 4064
7. Discovery of small molecule agonists for the bombesin receptor subtype 3 (BRS-3) based on an omeprazole lead
8. Conformationally constrained farnesoid X receptor (FXR) agonists: Naphthoic acid-based analogs of GW 4064
9. Thiol-based angiotensin-converting enzyme 2 inhibitors: P 1′ modifications for the exploration of the S 1′ subsite
10. Synthesis and evaluation of potent and selective β3 adrenergic receptor agonists containing heterobiaryl carboxylic acids
11. Acyclic, orally bioavailable ketone-based cathepsin K inhibitors
12. Thiol-based angiotensin-converting enzyme 2 inhibitors: P1′ modifications for the exploration of the S1′ subsite
13. Novel, potent P2–P3 pyrrolidine derivatives of ketoamide-based cathepsin K inhibitors
14. Semicarbazone-based inhibitors of cathepsin K, are they prodrugs for aldehyde inhibitors?
15. Ketoheterocycle-based inhibitors of cathepsin K: A novel entry into the synthesis of peptidic ketoheterocycles
16. P2–P3 conformationally constrained ketoamide-based inhibitors of cathepsin K
17. Acyclic cyanamide-based inhibitors of cathepsin K
18. A structural screening approach to ketoamide-based inhibitors of cathepsin K
19. Novel and potent cyclic cyanamide-based cathepsin K inhibitors
20. Potent and selective P2–P3 ketoamide inhibitors of cathepsin K with good pharmacokinetic properties via favorable P1′, P1, and/or P3 substitutions
21. Exploration of the P2–P3 SAR of aldehyde cathepsin K inhibitors
22. Orally bioavailable small molecule ketoamide-based inhibitors of cathepsin K
23. Design of small molecule ketoamide-based inhibitors of cathepsin K
24. Exploration of the P1 SAR of aldehyde cathepsin K inhibitors
25. P 2–P 3 conformationally constrained ketoamide-based inhibitors of cathepsin K
26. Exploration of the P 1 SAR of aldehyde cathepsin K inhibitors
27. Potent and selective P 2–P 3 ketoamide inhibitors of cathepsin K with good pharmacokinetic properties via favorable P 1′, P 1, and/or P 3 substitutions
28. Exploration of the P 2–P 3 SAR of aldehyde cathepsin K inhibitors
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