31 Results for "

GLYT2

" in MedChemExpress (MCE) Product Catalog:
Products (31)

31 Results for "GLYT2" in MCE Product Catalog:

  • Isoforms Recommended:
  • Targets Recommended:
Cat. No.: HY-103332S
CAS No.: 1159908-44-7
Purity:  98.1%
Synonyms: NA-Gly-d8
N-Arachidonylglycine-d8 is a deuterated labeled N-Arachidonylglycine . N-Arachidonylglycine (NA-Gly), a carboxylic analog of the endocannabinoid anandamide (AEA), is a GPR18 agonist (EC50 = 44.5 nM). Unlike AEA, N-Arachidonylglycine has no activity at either CB1 or CB2 receptors. N-Arachidonylglycine inhibits GLYT2 (IC50 = 5.1 μM). N-Arachidonylglycine also is an effective activator of endometrial cell migration [2] .
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Cat. No.: HY-P87792
Synonyms: GLYT2, NET1, SLC6A5, Sodium- and chloride-dependent glycine transporter 2, GLYT-2, GLYT2, Solute carrier family 6 member 5

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-113202S1
CAS No.: 2936622-19-2
Stearoyl-L-carnitine-d9 chloride is the deuterium labeled Stearoyl-L-carnitine chloride. Stearoyl-L-carnitine chloride, a fatty ester lipid molecule, is an endogenous metabolite. Stearoyl-L-carnitine chloride can be used as PKC inhibitor. Stearoyl-L-carnitine chloride accumulates in β cells, leading to arrest of insulin synthesis and energy deficiency in type 2 diabetes mouse. Stearoyl-L-carnitine chloride inhibits lecithin cholesterol acyltransferase (LCAT) in rat and rabbits plasma. Stearoyl-L-carnitine chloride acts as a metabolomics biomarker for Parkinson’s disease. Stearoyl-L-carnitine chloride is a less potent inhibitor of GlyT2 [2] .
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Cat. No.: HY-186238
CAS No.: 1440797-80-7
Target:  

GlyT 5-HT Receptor

Research Areas:  

Neurological Disease

VVZ-068 is a benzamide derivative and also a GlyT2/5HT2A antagonist. VVZ-068 alleviates neuropathic mechanical hyperalgesia in a rat model of mechanical allodynia. VVZ-068 is applicable for pain-related research .
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Cat. No.: HY-RS13314
Research Areas:  

Others

SLC6A5 Human Pre-designed siRNA Set A contains three designed siRNAs for SLC6A5 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS13316
Research Areas:  

Others

Slc6a5 Rat Pre-designed siRNA Set A contains three designed siRNAs for Slc6a5 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-148708A
Target:  

iGluR

Research Areas:  

Neurological Disease

Oleoyl-D-lysine sodium is a selective Glycine Transporter-2 (GlyT2) inhibitor based on lipid. Oleoyl-D-lysine sodium reverses neuropathic pain in mice, shows antidrowsiness effect on chronic neuropathic pain. Oleoyl-D-lysine sodium is safe and effective without respiratory depression .
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Cat. No.: HY-RS13315
Research Areas:  

Others

Slc6a5 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Slc6a5 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS05407
Research Areas:  

Others

GGTA1 Human Pre-designed siRNA Set A contains three designed siRNAs for GGTA1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-107527R
CAS No.: 495076-64-7
Research Areas:  

Neurological Disease

Org 25543 hydrochloride (Standard) is the analytical standard of Org 25543 (hydrochloride) (HY-107527). This product is intended for research and analytical applications. Org 25543 hydrochloride is a selective and irreversible GlyT2 inhibitor (IC50: 16 nM). Org 25543 hydrochloride has analgesia effect. Org 25543 hydrochloride ameliorates mechanical allodynia after partial sciatic nerve ligation injury in mice [2] .
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Cat. No.: HY-109067AR
CAS No.: 1440796-75-7
Synonyms: VVZ-149 hydrochloride (Standard)
Opiranserin hydrochloride (Standard) is the analytical standard of Opiranserin (hydrochloride) (HY-109067A). This product is intended for research and analytical applications. Opiranserin (VVZ-149) hydrochloride, a non-opioid and non-NSAID analgesic candidate, is a dual antagonist of glycine transporter type 2 (GlyT2) and serotonin receptor 2A (5HT2A), with IC50s of 0.86 and 1.3 μM, respectively. Opiranserin hydrochloride shows antagonistic activity on rP2X3 (IC50=0.87 μM). Opiranserin hydrochloride is development as an injectable agent for the treatment of postoperative pain [2] .
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