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SKF 89976A hydrochloride product vial image | Hello Bio
SKF 89976A hydrochloride product vial image | Hello Bio
Biological Data
Biological description | Potent, selective and competitive GAT-1 GABA uptake inhibitor. Selective for GAT-1 over GAT-2, GAT-3 and BGT-1 (IC50 values are 0.13, 550, 944 and 7210 µM respectively). Inhibits GABA uptake (Ki = 7 µM) and transmitter-gated currents (Ki = 0.03 µM). Shows anticonvulsant actions. Blood-brain barrier permeable. |
Solubility & Handling
Storage instructions | +4°C (desiccate) |
Solubility overview | Soluble in water (100mM, gentle warming) or DMSO (100mM) |
Important | This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use. |
Chemical Data
Chemical name | 1-(4,4-Diphenyl-3-butenyl)-3-piperidinecarboxylic acid hydrochloride |
Chemical structure | |
Molecular Formula | C22H25NO2.HCl |
PubChem identifier | 6917797 |
SMILES | Cl[H].OC(=O)C1CCCN(CC\C=C(\C2=CC=CC=C2)C2=CC=CC=C2)C1 |
InChiKey | SNGGBKYQZVAQKA-UHFFFAOYSA-N |
References for SKF 89976A hydrochloride
References are publications that support the biological activity of the product
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Identification and selective inhibition of the channel mode of the neuronal GABA transporter 1.
Krause S et al (2005) Mol Pharmacol 68(6) : 1728-35. -
Orally active and potent inhibitors of gamma-aminobutyric acid uptake.
Ali FE et al (1985) J Med Chem 28(5) : 653-60. -
Comparison of the anticonvulsant effects of two novel GABA uptake inhibitors and Ro 5-2807 in amygdaloid kindled rats.
Schwark WS et al (1985) Naunyn Schmiedebergs Arch Pharmacol 329(4) : 367-71.
Potent, selective, competitive GAT-1 GABA uptake inhibitor