BRL 54443
- CAS NO.:57477-39-1
- Empirical Formula: C14H18N2O
- Molecular Weight: 230.31
- MDL number: MFCD01861184
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-04-22 18:57:36
What is BRL 54443?
The Uses of BRL 54443
BRL-53443 is a potent 5-HT and dopamine receptor agonist. Neuroresearch product.
What are the applications of Application
BRL 54443 is a potent agonist at SR-1E and SR-1F
Definition
ChEBI: 3-(1-methyl-4-piperidinyl)-1H-indol-5-ol is a member of hydroxyindoles.
Biological Activity
A potent 5-ht 1E/1F receptor agonist (pEC 50 values are 8.5 and 8.6 respectively). Displays > 30-fold selectivity over other 5-HT and dopamine receptors (pK i 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-HT 1E , 1F , 1A , 1B , 1D , 2A , 2B , 2C , 4 , 7 , D 2 and D 3 receptors respectively). Induces 5-HT 2A receptor-mediated mouse aortic contraction in vitro (pEC 50 = 6.52). Active in vivo .
Storage
+4°C (desiccate)
References
1. a.m. brown, k. avenell, t j. young et al. brl 54443, a potent agonist with selectivity for human cloned 5-ht1e and 5-ht1f receptors. 1998. br.j.pharmacol. 123 233p.2. s. lightowler, t. stean, n. upton et al. 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. 1998. br.j.pharmacol. 123 237p.3. mckune cm, watts sw. characterization of the serotonin receptor mediating contraction in the mouse thoracic aorta and signal pathway coupling. j pharmacol exp ther. 2001 apr;297(1):88-95.4. janssen p, tack j, sifrim d et al. influence of 5-ht1 receptor agonists on feline stomach relaxation. eur j pharmacol. 2004 may 25;492(2-3):259-67.
Properties of BRL 54443
| Boiling point: | 431.5±45.0 °C(Predicted) |
| Density | 1.196 |
| storage temp. | Inert atmosphere,2-8°C |
| solubility | H2O: 50 mg/mL |
| form | solid |
| pka | 10.08±0.40(Predicted) |
| color | white |
Safety information for BRL 54443
Computed Descriptors for BRL 54443
New Products
5-Chlorothiophene-2-carboxylic acid 2-(2-Ethoxyphenoxy)ethyl bromide 1,3-Dibromo-2,2-dimethoxypropane 8-Bromo-3-methyl xanthine Maleic hydrazide 6-Methyl-2-(p-tolyl)imidazo[1,2-a]pyridine 3,4-Dihydroxyacetophenone 3,4-Dimethoxyacetophenone 4-Nitroacetophenone DL-Glutamic acid 3-Nitroacetophenone 4'-Chloro-3'-nitroacetophenone 2,3-Dihydro-5,6-dimethoxy-2-(4-piperidinylmethyl)-1H-inden-1-one hydrochloride 3-(4-Bromo-3-methyl-2-oxo-2,3-dihydro-1h-benzo[d]imidazol-1-yl)piperidine-2,6-dione 1-Boc-4-cyanopiperidine 2-Fluoro-6-iodobenzoic acid 3-Pyridineacrylic acid 3-Hydroxy-2-methylbenzoic acid 1,3-Dibromo-5-fluorobenzene 2-((2,6-Difluorobenzyl)(ethoxycarbonyl)amino)-4-((dimethylamino)methyl)-5-(4-nitrophenyl)thiophene-3-carboxylic acid [N(E)]-N-Ethylidene-2-methyl-2-propanesulfinamide 4-Isopropyl Thiophenol 6-(chloromethyl)pteridine-2,4-diamine monohydrochloride 2-Chlorophenyl diphenyl chloromethaneRelated products of tetrahydrofuran







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