19 results on '"Delorme, Daniel"'
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2. N,N-Diethyl-4-[(3-hydroxyphenyl)(piperidin-4-yl)amino] benzamide derivatives: The development of diaryl amino piperidines as potent δ opioid receptor agonists with in vivo anti-nociceptive activity in rodent models
3. SAR around (l)-S-adenosyl-l-homocysteine, an inhibitor of human DNA methyltransferase (DNMT) enzymes
4. Constrained (l-)-S-adenosyl-l-homocysteine (SAH) analogues as DNA methyltransferase inhibitors
5. SAR and biological evaluation of analogues of a small molecule histone deacetylase inhibitor N-(2-aminophenyl)-4-((4-(pyridin-3-yl)pyrimidin-2-ylamino)methyl)benzamide (MGCD0103)
6. Bisphosphonated fluoroquinolone esters as osteotropic prodrugs for the prevention of osteomyelitis
7. Design and synthesis of 4-[(s-triazin-2-ylamino)methyl]-N-(2-aminophenyl)-benzamides and their analogues as a novel class of histone deacetylase inhibitors
8. 4-(Heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs as a novel class of histone deacetylase inhibitors
9. N-(2-Amino-phenyl)-4-(heteroarylmethyl)-benzamides as new histone deacetylase inhibitors
10. A new class of small molecule RNA polymerase inhibitors with activity against Rifampicin-resistant Staphylococcus aureus1
11. Substituted N-(2-aminophenyl)-benzamides, (E)-N-(2-aminophenyl)-acrylamides and their analogues: Novel classes of histone deacetylase inhibitors
12. Substituted coumarins as potent 5-lipoxygenase inhibitors
13. Novel non-nucleobase inhibitors of Staphylococcus aureus DNA polymerase IIIC
14. (2-Amino-phenyl)-amides of ω-substituted alkanoic acids as new histone deacetylase inhibitors
15. Design and synthesis of a novel class of histone deacetylase inhibitors
16. Asymmetric synthesis of diarylmethylamines: preparation of selective opioid delta receptor ligands
17. Synthesis of 5-thialdopentopyranoside via dithioacetal rearrangement and glycosidation to give pseudodisaccharides
18. The asymmetric synthesis of α-chloro α-alkyl and α-methyl α-alkyl phosphonic acids of high enantiomeric purity.
19. Mild cleavage of methoxymethyl (MOM) ethers with trimethylsilyl bromide
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