Discovery of diphenyl amine based sodium channel blockers, effective against hNa v 1.2
DP Hudgens, C Taylor, TW Batts, MK Patel…
Index: Hudgens, Debjani P.; Taylor, Catherine; Batts, Timothy W.; Patel, Manoj K.; Brown, Milton L. Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 24 p. 8366 - 8378
Full Text: HTML
Citation Number: 12
Abstract
The development of new therapies for chronic pain is an area of unmet medical need. Central to pathways of chronic pain is the upregulation of voltage-gated sodium channels. The use of tricyclic antidepressants, which also have sodium channel activity, in chronic pain therapy prompted us to develop novel compounds from this scaffold. Herein, we show that the tricyclic moiety is not needed for effective inhibition of the [3H]-BTX binding site and ...
Related Articles:
[Satoh, Tsuyoshi; Nakamura, Akira; Iriuchijima, Atsuko; Hayashi, Yasumasa; Kubota, Ko-Ichi Tetrahedron, 2001 , vol. 57, # 48 p. 9689 - 9696]
[Howden,M.E.H. et al. Journal of the American Chemical Society, 1966 , vol. 88, p. 1732 - 1742]
[Kurosawa, Kazu; Tsujita, Tsuyoshi Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 8 p. 2391 - 2394]
[Gualtieri; Teodori; Bellucci; Pesce; Piacenza Journal of Medicinal Chemistry, 1985 , vol. 28, # 11 p. 1621 - 1628]
[Johnson; Petersen; Schneider Journal of the American Chemical Society, 1947 , vol. 69, p. 74,77]