中文名 | WAY-213613 |
英文名 | N-[4-(2-BROMO-4,5-DIFLUOROPHENOXY)PHENYL]-L-ASPARAGINE |
英文别名 | WAY-213613 N-[4-(2-BROMO-4,5-DIFLUOROPHENOXY)PHENYL]-L-ASPARAGINE |
CAS | 868359-05-1 |
化学式 | C16H13BrF2N2O4 |
分子量 | 415.19 |
溶解度 | 溶于DMSO |
存储条件 | -20℃ |
产品用途 | WAY-213613 is a potent, non-substrate inhibitor of EAAT2 (GLT-1) that displays > 44-fold selectivity over EAAT1 and EAAT3 (IC50 values are 85, 3787 and 5004 nM for EAAT2, EAAT3 and EAAT1 respectively). WAY-213613 exhibits no activity towards ionotropic and metabotropic glutamate receptors. |
靶点 | Human EAAT2 Human EAAT3 Human EAAT1 |
参考资料 展开查看 | 1: Karatas-Wulf U, Koepsell H, Bergert M, Sönnekes S, Kugler P. Protein kinase C-dependent trafficking of glutamate transporters excitatory amino acid carrier 1 and glutamate transporter 1b in cultured cerebellar granule cells. Neuroscience. 2009 Jul 7;161(3):794-805. doi: 10.1016/j.neuroscience.2009.04.017. Epub 2009 Apr 11. PubMed PMID: 19364521. 2: Dunlop J, McIlvain HB, Carrick TA, Jow B, Lu Q, Kowal D, Lin S, Greenfield A, Grosanu C, Fan K, Petroski R, Williams J, Foster A, Butera J. Characterization of novel aryl-ether, biaryl, and fluorene aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT2. Mol Pharmacol. 2005 Oct;68(4):974-82. Epub 2005 Jul 13. PubMed PMID: 16014807. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.409 ml | 12.043 ml | 24.085 ml |
5 mM | 0.482 ml | 2.409 ml | 4.817 ml |
10 mM | 0.241 ml | 1.204 ml | 2.409 ml |
5 mM | 0.048 ml | 0.241 ml | 0.482 ml |
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