L-655,708
Tocris Bioscience, part of Bio-Techne | Catalog # 1327
Benzodiazepine inverse agonist; selective for α5-containing GABAA receptors
Key Product Details
Description
Benzodiazepine inverse agonist; selective for α5-containing GABAA receptors
Product Description
L-655,708 is a potent, selective inverse agonist for the benzodiazepine site of GABAA receptors containing the α5 subunit (Ki = 0.45 nM). Displays 50-100-fold selectivity over GABAA receptors containing α1, α2, α3 or α6 subunits in combination with β3 and γ2. Enhances LTP in a mouse hippocampal slice model and increases spatial learning, without displaying proconvulsant activity.Product Specifications
Molecular Weight
341.37
Formula
C18H19N3O4
Storage
Desiccate at +4°C
Purity
≥98% (HPLC)
Chemical Name
11,12,13,13a-Tetrahydro-7-methoxy-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylic acid, ethyl ester
CAS Number
130477-52-0
PubChem ID
5311203
InChI Key
YKYOQIXTECBVBB-AWEZNQCLSA-N
SMILES
O=C(N3[C@]([H])2CCC3)C4=C(C=CC(OC)=C4)N1C2=C(C(OCC)=O)N=C1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 8.53 | 25 |
Preparing Stock Solutions
for L-655,708
The following data is based on the product molecular weight 341.37
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.25 mM | 11.72 mL | 58.59 mL | 117.17 mL |
| 1.25 mM | 2.34 mL | 11.72 mL | 23.43 mL |
| 2.5 mM | 1.17 mL | 5.86 mL | 11.72 mL |
| 12.5 mM | 0.23 mL | 1.17 mL | 2.34 mL |
Calculators
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Background References
References are publications that support the biological activity of the product.
- Quirk [3H]L-655,708, a novel ligand selective for the benzodiazepine site of GABAA receptors which contain the α5 subunit. Neuropharmacology 1996 PMID: 9014149
- Sur Rat and human hippocampal α5 subunit-containing γ-aminobutyric acidA receptors have α5α3γ2 pharmacological characteristics. Mol.Pharmacol. 1998 PMID: 9804628
- Atack L-655,708 enhances cognition in rats but is not proconvulsant at a dose selective for α5-containing GABAA receptors. Neuropharmacology 2006 PMID: 17046030
Product Specific Notices for L-655,708
For research use only
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