198348-90-2Relevant academic research and scientific papers
3-Trifluoromethyl-4-nitro-5-arylpyrazoles are novel KATP channel agonists
Peat, Andrew J.,Townsend, Claire,McKay, M. Craig,Garrido, Dulce,Terry, Christopher M.,Wilson, Jayme L. R.,Thomson, Stephen A.
, p. 813 - 816 (2007/10/03)
This communication describes the discovery and synthesis of a series of 3-trifluoromethyl-4-nitro-5-arylpyrazoles as potent KATP channel agonists. The most potent compound reported is ca. 100-fold more potent than diazoxide and exhibits selectivity for the SUR1 KATP channel subtype. The 4-nitro substitutent on the pyrazole ring was required for activity, and limited SAR suggests that the de-protonated pyrazole maybe the active species.
Nitropyrazoles: 10. N-nitration of 3(5)-substituted pyrazoles
Dalinger,Litosh,Shevelev
, p. 1149 - 1153 (2007/10/03)
A number of substituted N-nitropyrazoles were prepared by direct nitration of substituted pyrazoles. The dependence of the direction of nitration on the reaction conditions was studied.
