DL-TBOA

  Cat. No.:  DC28201   Featured
Chemical Structure
205309-81-5
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Field of application
DL-TBOA is a potent non-transportable inhibitor of excitatory amino acid transporters with IC50s of 70 μM, 6 μM and 6 μM for excitatory amino acid transporter-1 (EAAT1), EAAT2 and EAAT3, respectively. DL-TBOA inhibits the uptake of [14C]glutamate in COS-1 cells expressing the human EAAT1 and EAAT2 with Ki valuesof 42 μM and 5.7 μM, respectively. DL-TBOA blocks EAAT4 and EAAT5 in a competitive manner with Ki values of 4.4 μM and 3.2 μM, respectively.
Cas No.: 205309-81-5
Chemical Name: DL-TBOA
Synonyms: D-Aspartic acid, 3-(phenylmethoxy)-, (3R)-rel-;DL-TBOA;DL-threo-β-Benzyloxyasparticacid;2-amino-3-phenylmethoxybutanedioic acid;2-Amino-3-(benzyloxy)succinic acid;(2S,3S)-2-Amino-3-benzyloxy-succinic acid;threo-beta-benzyloxyaspartic acid;D,L-threo-beta-benzyloxyaspartate;HMS3267D15;BDBM50247191;DL-2-amino-3-(benzyloxy)succinic acid;Q27166729
SMILES: O(CC1C=CC=CC=1)C(C(=O)O)C(C(=O)O)N
Formula: C11H13NO5
M.Wt: 239.224623441696
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC73617 NV-6297 NV-6297 (NV6297) is a potent, selective mTORC1 pathway signaling inhibitor without inhibition on mTORC2, inhibits S6K1 phosphorylation (pS6K1 T389) in MCF7 cells with IC50 of 120 nM, directly and selectively targets GLUT-1.
DC48737 TFB-TBOA TFB-TBOA (CF3-Bza-TBOA) is a potent glutamate transporter blocker that potently suppresses the activity of glial transporters. TFB-TBOA shows IC50 values of 22, 17, and 300 nM for glutamate transporters EAAT1, EAAT2, and EAAT3 respectively in an uptake assay using cells transiently expressing EAATs.
DC28201 DL-TBOA DL-TBOA is a potent non-transportable inhibitor of excitatory amino acid transporters with IC50s of 70 μM, 6 μM and 6 μM for excitatory amino acid transporter-1 (EAAT1), EAAT2 and EAAT3, respectively. DL-TBOA inhibits the uptake of [14C]glutamate in COS-1 cells expressing the human EAAT1 and EAAT2 with Ki valuesof 42 μM and 5.7 μM, respectively. DL-TBOA blocks EAAT4 and EAAT5 in a competitive manner with Ki values of 4.4 μM and 3.2 μM, respectively.
DC11145 WAY213613 WAY-213613 (WAY213613) is a potent, non-substrate inhibitor of EAAT2 (GLT-1) with IC50 of 85 nM, displays > 44-fold selectivity over EAAT1 and EAAT3; also exhibits no activity towards ionotropic and metabotropic glutamate receptors.
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