JV-methyl-D-aspartic acid

Nakazawa, T., Shimura, M., Endo, S., Takahashi, H., Mori, N., and Tamai, M. (2005). jV-Methyl-D-Aspartic acid suppresses Akt activity through protein phosphatase in retinal ganglion cells. Mol. Vis. 11, 1173-1182. 

Ornstein, P.L., Schoepp, D.D., Arnold, M.B., Leander, J.D., Lodge, D., Paschal, J.W., and Elzey, T., 4-(TetrazolylaIkyl)piperidine-2-carboxylic acids. Potent and selective JV-methyl-D-aspartic acid receptor antagonists with a short duration of action, J. Med. Chem., 34, 90, 1991. 

JV-methyl-D-aspartic acid (NMDA) receptor, 1373, 1374,4006 antagmiism, 1249 antagmiist, 1246... 

Quinoxaline 1,4-dioxides possess antibacterial activity, " as well as being fungicides, insecticides, and herbicides. Quinoxaline-2-carboxylic acid 1,4-dioxide has been isolated from cultures of Sireplomyces ambrofaciens and this compound has been shown to have antibiotic properties. Echinomycin, from the quinoxaline-peptide antibiotic family, contains one or more quinoxaline rings and is an antitumor agent. Quinoxaline derivatives are also antagonists at the jV-methyl-D-aspartate (NMDA) receptor of the glycine modulatory site. Poly(phenylquinoxalines) are used as high temperature polymers. 

Kashiwagi K, Wifliams K, Igarashi K (2007) Anthraquinone polyamines novel channel blockers of JV-methyl-D-aspartate receptors. Amino Acids 33 299-304 Masuko T, Kashiwagi K, Kuno T et al (1999) A regulatory domain (R1-R2) in the amino terminus of the JV-methyl-D-aspartate receptor effects of spermine, protons, and ifenprodU, and structural similarity to bacterial leudne/isoleudne/valine binding protein. Mol Pharmacol 55 957-969 Masuko T, Kusama-Eguchi K, Sakata K et al (2003) Polyamine transport, accumulation, and release in brain. J Neurochem 84 610-617... 

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