1. Membrane Transporter/Ion Channel Neuronal Signaling
  2. GABA Receptor
  3. SR-THAP

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.

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SR-THAP

SR-THAP Chemical Structure

CAS No. : 3098361-74-8

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Description

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].

In Vitro

SR-THAP (0-1000 μM; 120 min preincubation + 3 min uptake) inhibits hGAT3C316S mutant-mediated [3H]GABA uptake in HEK293T cells with reduced potency (IC50 = 10.6 μM) compared to wild-type hGAT3[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

517.61

Formula

C31H35NO6

CAS No.
SMILES

COC1=CC=C(C=C1)C(C2=CC=C(C=C2)OC)(C3=CC=C(C=C3)OC)/C=C/CN4CCC[C@]4([H])[C@@H](C(O)=O)O

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Please store the product under the recommended conditions in the Certificate of Analysis.

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SR-THAP
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HY-181961
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