36 Results for "

GABA uptake

" in MedChemExpress (MCE) Product Catalog:
Products (36)

36 Results for "GABA uptake" in MCE Product Catalog:

16
16 Publications Verification
Cat. No.: HY-B0211
CAS No.: 1744-22-5
Synonyms: PK 26124
Research Areas:  

Neurological Disease Cancer

Riluzole is an anticonvulsant agent and belongs to the family of use-dependent Na + channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM.
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16
16 Publications Verification
Cat. No.: HY-B0211A
CAS No.: 850608-87-6
Synonyms: PK 26124 hydrochloride
Research Areas:  

Neurological Disease Cancer

Riluzole hydrochloride is an anticonvulsant agent and belongs to the family of use-dependent Na + channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM.
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1
1 Cited Publications
Cat. No.: HY-16974
CAS No.: 1093861-60-9
Research Areas:  

Infection

Afoxolaner is an orally active isoxazoline insecticide/acaricide against Ixodes scapularis in dogs. Afoxolaner acts on the insect γ-aminobutyric acid receptor (GABA) and glutamate receptors, inhibiting GABA & glutamate-regulated uptake of chloride ions, resulting in excess neuronal stimulation and death of the arthropod .
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1
1 Cited Publications
Cat. No.: HY-N2368
CAS No.: 499-04-7
Arecaidine is a GABA transport system inhibitor. Arecaidine inhibits the proliferation of oral mucosal fibroblasts, increases the secretion of IL-6, TGF-β and TNF-α in cells, downregulates the expression of PPAR-γ and PCK1 in cells, and upregulates the expression of TGF-β1 . Arecaidine inhibits the uptake of γ-aminobutyric acid and β-alanine by the central nervous system of cats . Arecaidine inhibits hPAT1-mediated L-[ 3H]proline uptake in cells. Arecaidine can be used in research related to neurological diseases .
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1
1 Cited Publications
Cat. No.: HY-69359
CAS No.: 498-95-3
Synonyms: (±)-β-Homoproline; Hexahydronicotinic acid; 3-Carboxypiperidine
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Nipecotic acid ((±)-β-Homoproline) is a potent inhibitor of neuronal and glial-aminobutyric acid (GABA) uptake in vitro. Nipecotic acid can also directly activate GABAA-like chloride channels, with an EC50 of approximately 300 μM .
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1
1 Cited Publications
Cat. No.: HY-N2368A
CAS No.: 6018-28-6
Arecaidine hydrochloride, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine hydrochloride is a substrate of H +-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake .
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1
1 Cited Publications
Cat. No.: HY-N2368B
CAS No.: 6013-57-6
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Arecaidine hydrobromide, a pyridine alkaloid, is a potent GABA uptake inhibitor. Arecaidine hydrobromide is a substrate of H +-coupled amino acid transporter 1 (PAT1, SLC36A1) and competitively inhibits L-proline uptake .
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Cat. No.: HY-W067716
CAS No.: 59981-63-4
Synonyms: (S)-Spinacine
Spinacine ((S)-Spinacine) is a GABA uptake inhibitor. Spinacine enhances synaptic GABA effects via inhibition of gamma-aminobutyric acid uptake in cerebral cortex slices. Spinacine inhibits reflex responses of ventral roots in isolated spinal cord. Spinacine inhibits motor activity and reduces approaches to water dispensers in conflict situations. Spinacine raises pain sensitivity threshold via subarachnoidal injection .
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Cat. No.: HY-100800
CAS No.: 38090-53-8
Purity:  99.33%
Synonyms: trans-4-Aminocrotonic acid
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

TACA (trans-4-Aminocrotonic acid) is a potent agonist of GABAA and GABAC receptors (KD= 0.6 μM). TACA also is GABA uptake inhibitor and substrate for GABA-T. TACA produces late biphasic responses in the MPG neurons .
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Cat. No.: HY-124030
CAS No.: 70030-11-4
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

3-Hydroxyphenazepam is an active metabolite of Cinazepam. Cinazepam is a GABAA receptor agonist. 3-Hydroxyphenazepam can inhibit synaptosomal transporter-mediated [ 3H]GABA uptake .
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Cat. No.: HY-103509
CAS No.: 184845-18-9
Purity:  99.09%
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

NNC 05-2090 hydrochloride is a GABA uptake inhibitor and inhibitor of the β-GABA transporter (BGT-1) (IC50< /sub>: 10.6 μM). NNC 05-2090 hydrochloride also inhibits mGAT2 with a Ki value of 1.4 μM. NNC 05-2090 has anticonvulsant activity and can be used in the study of epilepsy and neurological diseases .
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Cat. No.: HY-W103105
CAS No.: 53786-28-0
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

R 29676 is a neuroleptic agent and inhibits sodium-dependent GABA binding (GABA uptake) .
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Cat. No.: HY-103534
CAS No.: 110283-66-4
Purity:  99.60%
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

CI-966 hydrochloride is a potent, selective, orally active and brain-penetrant inhibitor of the GABA transporter GAT-1, with IC50s of 0.26 μM and 1.2 μM for hGAT-1, rGAT-1, respectively. CI-966 hydrochloride shows more than 200-fold selectivity over GAT-2, GAT-3, and BGT-3. CI-966 hydrochloride exhibits anticonvulsant and neuroprotective activities .
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Cat. No.: HY-B0211R
CAS No.: 1744-22-5
Synonyms: PK 26124 (Standard)
Riluzole (Standard) is the analytical standard of Riluzole. This product is intended for research and analytical applications. Riluzole is an anticonvulsant agent and belongs to the family of use-dependent Na + channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM.
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Cat. No.: HY-16974R
CAS No.: 1093861-60-9
Afoxolaner (Standard) is the analytical standard of Afoxolaner. This product is intended for research and analytical applications. Afoxolaner is an orally active isoxazoline insecticide/acaricide against Ixodes scapularis in dogs. Afoxolaner acts on the insect γ-aminobutyric acid receptor (GABA) and glutamate receptors, inhibiting GABA & glutamate-regulated uptake of chloride ions, resulting in excess neuronal stimulation and death of the arthropod .
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Cat. No.: HY-W067716R
CAS No.: 59981-63-4
Synonyms: (S)-Spinacine (Standard)
Spinacine (Standard) is the analytical standard of Spinacine (HY-W067716). This product is intended for research and analytical applications. Spinacine ((S)-Spinacine) is a GABA uptake inhibitor. Spinacine enhances synaptic GABA effects via inhibition of gamma-aminobutyric acid uptake in cerebral cortex slices. Spinacine inhibits reflex responses of ventral roots in isolated spinal cord. Spinacine inhibits motor activity and reduces approaches to water dispensers in conflict situations. Spinacine raises pain sensitivity threshold via subarachnoidal injection .
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Cat. No.: HY-B0211S1
Synonyms: PK 26124-13C6
Riluzole- 13C6 (PK 26124- 13C6) is 13C labeled Riluzole. Riluzole is an anticonvulsant agent and belongs to the family of use-dependent Na + channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM.
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Cat. No.: HY-155238
CAS No.: 1520073-91-9
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

E2730 is a noncompetitive but selective inhibitor of gamma-aminobutyric acid (GABA) transporter 1 (GAT1) with orally available and antiepileptic activity. E2730-mediated GAT1 inhibition is positively correlated with environmental GABA levels and selectively inhibits GAT1-mediated GABA uptake. E2730 (5-50 mg/kg; po) in rat amygdala ignition model, and in mouse cornea ignition (5-50 mg/kg), drug resistance 6Hz-44mA has demonstrated in vivo efficacy in models of psychomotor epilepsy (5-50 mg/kg), fragile X syndrome (2.5-300 mg/kg), and Dravet syndrome (10 mg/kg, 20 mg/kg) .
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Cat. No.: HY-129464
CAS No.: 127586-66-7
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

NO-711ME is a prodrug of NO-711. NO-711 is a potent and selective GABA uptake inhibitor .
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Cat. No.: HY-N9407
CAS No.: 18513-76-3
Guvacine ethyl ester (3.1b) is an alkaloid that can be found in betel nut. Guvacine ethyl ester can be used in the synthesis of GABA uptake inhibitor .
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