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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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B129734-10mg | 10mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $83.90 | |
B129734-50mg | 50mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $346.90 | |
B129734-100mg | 100mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $624.90 |
Selective agonist at 5-HT 1E and 5-HT 1F receptors
Synonyms | GTPL3927 | AC-32702 | Biomol-NT_000107 | CHEBI:92321 | CS-2025 | NCGC00025019-01 | SB19516 | EX-A2195 | HMS3651N17 | NCGC00015134-13 | NCGC00025019-03 | BCP9000451 | GS-6123 | HMS3267M18 | MFCD01861184 | HMS3884P18 | BCPP000316 | NCGC00015134-05 | 5-Hydro |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | BRL 54443 is a potent SR-1E and SR-1F agonist (pEC50 values are 8.5 and 8.6 respectively). It induces SR-2A receptor-mediated mouse aortic contraction in vitro (pEC50 = 6.52). BRL 54443 displays > 30-fold selectivity over other serotonin and dopamine rece |
Storage Temp | Store at 2-8°C |
Shipped In | Wet ice |
Grade | Moligand™ |
Action Type | AGONIST |
Mechanism of action | Agonist of 5-ht 1e receptor;Agonist of 5-HT 1F receptor |
Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | BRL 54443 is a 5-HT1E and 5-HT1F receptor agonist with pKi of 8.7 and 9.25, respectively, with a weak binding affinity for 5-HT1A, 5-HT1B, 5-HT1D receptors. |
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IUPAC Name | 3-(1-methylpiperidin-4-yl)-1H-indol-5-ol |
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INCHI | InChI=1S/C14H18N2O/c1-16-6-4-10(5-7-16)13-9-15-14-3-2-11(17)8-12(13)14/h2-3,8-10,15,17H,4-7H2,1H3 |
InChi Key | WKNFADCGOAHBPG-UHFFFAOYSA-N |
Canonical SMILES | CN1CCC(CC1)C2=CNC3=C2C=C(C=C3)O |
Isomeric SMILES | CN1CCC(CC1)C2=CNC3=C2C=C(C=C3)O |
Alternate CAS | 57477-39-1 |
PubChem CID | 2438 |
Molecular Weight | 230.31 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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E1520129 | Certificate of Analysis | Dec 07, 2022 | B129734 |
Solubility | DMSO 46 mg/mL Water <1 mg/mL Ethanol 2 mg/mL |
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1. McKune CM & Watts SW. (2001) Characterization of the serotonin receptor mediating contraction in the mouse thoracic aorta and signal pathway coupling.. J Pharmacol Exp Ther, 297 (88-95). [PMID:11259531] |