5 Results for "

hGlyT1

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "hGlyT1" in MCE Product Catalog:

  • Isoforms Recommended:
Cat. No.: HY-107526
CAS No.: 405225-21-0
Synonyms: (Rac)-NFPS
Target:  

GlyT

Research Areas:  

Neurological Disease

NFPS is a selective, non-competitive glycine transporter-1 (GlyT1) inhibitor with IC50s of 2.8 nM and 9.8 nM for hGlyT1 and rGlyT1, respectively [1]. NFPS exerts neuroprotection via glyR alpha1 subunit in the rat model of transient focal cerebral ischaemia and reperfusion .
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Cat. No.: HY-100416A
CAS No.: 1779796-27-8
Purity:  98.69%
Target:  

GlyT

Research Areas:  

Neurological Disease

LY2365109 hydrochloride is a potent and selective GlyT1 inhibitor, with an IC50 of 15.8 nM for glycine uptake in cells over-expressing hGlyT1a [1] .
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Cat. No.: HY-100416
CAS No.: 868265-28-5
Target:  

GlyT

Research Areas:  

Neurological Disease

LY2365109 is a potent and selective GlyT1 inhibitor, with an IC50 of 15.8 nM for glycine uptake in cells over-expressing hGlyT1a [1] .
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Cat. No.: HY-100416AR
CAS No.: 1779796-27-8
Research Areas:  

Neurological Disease

LY2365109 (hydrochloride) (Standard) is the analytical standard of LY2365109 (hydrochloride) (HY-100416A). This product is intended for research and analytical applications. LY2365109 hydrochloride is a potent and selective GlyT1 inhibitor, with an IC50 of 15.8 nM for glycine uptake in cells over-expressing hGlyT1a [1] .
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Cat. No.: HY-181961
CAS No.: 3098361-74-8
SR-THAP is a γ-aminobutyric acid transporter 3 (GAT3) inhibitor with an IC50 of 4.9 μM, and exhibits 42-fold and 23-fold selectivity over GAT1 and GlyT1, respectively. SR-THAP inhibits GABA uptake in mammalian cells. SR-THAP is applicable to the research of epilepsy, Alzheimer's disease and ischemic stroke [1].
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