Dantrolene analogues revisited: general synthesis and specific functions capable of discriminating two kinds of Ca 2+ release from sarcoplasmic reticulum of mouse …

…, H Aoyama, T Ikemoto, Y Kihara, T Hiramatsu…

Index: Hosoya, Takamitsu; Aoyama, Hiroshi; Ikemoto, Takaaki; Kihara, Yasutaka; Hiramatsu, Toshiyuki; Endo, Makoto; Suzuki, Masaaki Bioorganic and Medicinal Chemistry, 2003 , vol. 11, # 5 p. 663 - 673

Full Text: HTML

Citation Number: 33

Abstract

The general synthesis of dantrolene analogues with various substituents on its phenyl ring has been developed via palladium-catalyzed cross-coupling reactions, the Stille or Suzuki reaction, as the key step. The effects of synthesized analogues have been evaluated by two kinds of Ca2+ release modes from sarcoplasmic reticulum (SR) of mouse skeletal muscle fibers based on:(1) the measurement of twitch contraction caused by the physiological ...

Related Articles:

A practical one-pot synthesis of 5-aryl-2-furaldehydes

[McClure; Roschangar; Hodson; Millar; Osterhout Synthesis, 2001 , # 11 p. 1681 - 1685]

Furan-2-ylmethylene thiazolidinediones as novel, potent, and selective inhibitors of phosphoinositide 3-kinase γ

[Journal of Medicinal Chemistry, , vol. 49, # 13 p. 3857 - 3871]

Structure–Activity relationships of novel anti-Malarial agents. Part 4: N-(3-Benzoyl-4-tolylacetylaminophenyl)-3-(5-aryl-2-furyl) acrylic acid amides

[Bioorganic and Medicinal Chemistry Letters, , vol. 12, # 19 p. 2681 - 2683]

A practical one-pot synthesis of 5-aryl-2-furaldehydes

[Synthesis, , # 11 p. 1681 - 1685]

More Articles...