A novel, potent, and selective 5-HT7 antagonist:(R)-3-(2-(2-(4-methylpiperidin-1-yl)-ethyl) pyrrolidine-1-sulfonyl) phenol (SB-269970)

PJ Lovell, SM Bromidge, S Dabbs…

Index: Journal of Medicinal Chemistry, , vol. 43, # 3 p. 342 - 345

Full Text: HTML

Citation Number: 234

Abstract

... Revue / Journal Title. Journal of medicinal chemistry ISSN 0022-2623 CODEN JMCMAR Source / Source. 2000, vol. 43, n o 3, pp. 342-345 (17 ref.) Langue / Language. Anglais Editeur / Publisher. American Chemical Society, Columbus, OH, ETATS-UNIS (1963) (Revue) ...

Related Articles:

Transition state analogue discrimination by related purine nucleoside phosphorylases

[Journal of the American Chemical Society, , vol. 128, # 22 p. 7126 - 7127]

Synthesis and biological evaluation of potential 5-HT 7 receptor PET radiotracers

[European Journal of Medicinal Chemistry, , vol. 46, # 8 p. 3455 - 3461]

Transition state analogue discrimination by related purine nucleoside phosphorylases

[Journal of the American Chemical Society, , vol. 128, # 22 p. 7126 - 7127]

Endomorphin-1 analogues containing β-proline are μ-opioid receptor agonists and display enhanced enzymatic hydrolysis resistance

[Journal of Medicinal Chemistry, , vol. 45, # 12 p. 2571 - 2578]

Transition state analogue discrimination by related purine nucleoside phosphorylases

[Journal of the American Chemical Society, , vol. 128, # 22 p. 7126 - 7127]

More Articles...