5 results for "EAAT2/GLT1 Small Molecules and Peptides" in 产品

EAAT2/GLT1 Small Molecules and Peptides

GLT1 is the major glial glutamate transporter that takes up more than 90% of glutamate from the synapse. GLT1b is a splice variant that contains 11 unique amino acids at the C-terminus that encode a PDZ binding domain. GLT1b was initially believed to be the neuronal isoform of GLT1, but it now appears that GLT1b is localized to astrocytes in the normal brain and to neurons in pathological conditions. In Lou Gehrig's Disease, GLT1a is decreased, while GLT1b is increased. There are also different expressions in hypoxic cells, which have not yet been fully elucidated.

Selective non-transportable inhibitor of EAATs

Chemical Name: DL-threo-β-Benzyloxyaspartic acid
Purity: ≥98%
Selective non-transportable inhibitor of EAATs
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Potent and selective positive allosteric modulator of EAAT2

Chemical Name: 3-((4-Cyclohexylpiperazin-1-yl)(1-phenethyl-1H-tetrazol-5-yl)methyl)-6-methoxyquinolin-2(1H)-one
Purity: ≥98%
Potent and selective positive allosteric modulator of EAAT2
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Potent, non-substrate EAAT2 inhibitor

Chemical Name: N-[4-(2-Bromo-4,5-difluorophenoxy)phenyl]-L-asparagine
Purity: ≥98%
Potent, non-substrate EAAT2 inhibitor
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Potent competitive inhibitor of L-glutamate uptake

Chemical Name: 7-Chloro-4-hydroxyquinoline-2-carboxylic acid
Purity: ≥98%
Potent competitive inhibitor of L-glutamate uptake
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EAAT2 (GLT-1)-selective non-transportable inhibitor of L-glutamate and L-aspartate uptake

Chemical Name: (2S,3S,4R)-2-Carboxy-4-isopropyl-3-pyrrolidineacetic acid
EAAT2 (GLT-1)-selective non-transportable inhibitor of L-glutamate and L-aspartate uptake
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