Synthesis and pharmacology of N1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists
The binding site for competitive NMDA receptor antagonists is on the NR2 subunit, of which there are four types (NR2A-D). Typical antagonists such as (R)-AP5 have a subunit selectivity of NR2A > NR2B > NR2C > NR2D. The competitive NMDA receptor antagonist
Morley, Richard M.,Tse, Heong-Wai,Feng, Bihua,Miller, Jacqueline C.,Monaghan, Daniel T.,Jane, David E.
p. 2627 - 2637
(2007/10/03)
Properties of the Liquid Crystals formed by Certain 4-Alkoxy-N-(2-phenanthrylmethylene)anilines
The liquid crystal transition temperatures of twelve 4-alkoxy-N-(2-phenanthrylmethylene)anilines are reported and compared with those of corresponding members of similar homologous series of azomethines.Differences in liquid crytal thermal stability between comparable azomethines in which the -CH=N- linkage is reversed are discussed.
Brown, John W.,Byron, David J.,Fawcett, Linda A.,Wilson, Robert C.,Gillyon, Andrew M.,et al.
p. 1593 - 1596
(2007/10/02)
AMINO-OXY-DERIVATIVES. V. SOME O-ETHERS OF 2-SUBSTITUTED
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MAMALIS,GREEN,OUTRED,RIX
p. 1829 - 1843
(2007/10/04)
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