BRL 54443
Tocris Bioscience, part of Bio-Techne | Catalog # 1129
Potent 5-ht1E and 5-HT1F agonist
Discontinued Product
1129 has been discontinued.
View all 5-HT1E Receptor Agonists products.
Key Product Details
Description
Potent 5-ht1E and 5-HT1F agonist
Product Description
BRL 54443 is a potent 5-ht1E/1F receptor agonist (pEC50 values are 8.5 and 8.6 respectively). Displays > 30-fold selectivity over other 5-HT and dopamine receptors (pKi values are 8.7. 8.9, 7.2, 6.9, 7.2, 5.9, 7.0, 6.5, < 6, < 6, 6.3 and 6.2 for human 5-HT1E, 1F, 1A, 1B, 1D, 2A, 2B, 2C, 4, 7, D2 and D3 receptors respectively). Induces 5-HT2A receptor-mediated mouse aortic contraction in vitro (pEC50 = 6.52). Active in vivo.Product Specifications
Molecular Weight
230.31
Formula
C14H18N2O
Storage
Desiccate at +4°C
Chemical Name
5-Hydroxy-3-(1-methylpiperidin-4-yl)-1H-indole
CAS Number
57477-39-1
PubChem ID
2438
InChI Key
WKNFADCGOAHBPG-UHFFFAOYSA-N
SMILES
CN1CCC(CC1)C1=CNC2=CC=C(O)C=C12
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 | 50 |
Preparing Stock Solutions
for BRL 54443
The following data is based on the product molecular weight 230.31
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 |
|---|---|---|---|
| 0.5 mM | 8.68 mL | 43.42 mL | 86.84 mL |
| 2.5 mM | 1.74 mL | 8.68 mL | 17.37 mL |
| 5 mM | 0.87 mL | 4.34 mL | 8.68 mL |
| 25 mM | 0.17 mL | 0.87 mL | 1.74 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Brown BRL 54443, a potent agonist with selectivity for human cloned 5-HT1E and 5-HT1F receptors. Br.J.Pharmacol.
- Lightowler Effect of BRL 54443 (3-(1-methylpiperidin-4-yl)-1H-indol-5-ol), a 5-HT1E/1F receptor agonist, on general behaviour and maximal electroshock seizure threshold in the rat. Br.J.Pharmacol.
- McKune and Watt Characterization of the serotonin receptor mediating contraction in the mouse thoracic aorta and signal pathway coupling. J.Pharmacol.Exp.Ther. 2001 PMID: 11259531
Product Specific Notices for BRL 54443
For research use only
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