Biological Activity
5-HT1A antagonist. More active and selective than spiperone. Also a very potent α2C adrenergic receptor antagonist.
Technical Data
M. Wt | 379.46 |
Formula | C22H25N3O3 |
Storage | Store at RT |
CAS Number | 1054-88-2 |
PubChem ID | 5268 |
InChI Key | JVGBTTIJPBFLTE-UHFFFAOYSA-N |
Smiles | O=C1NCN(C2=CC=CC=C2)C11CCN(CC2COC3=CC=CC=C3O2)CC1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMSO | 3.79 | 10 |
Preparing Stock Solutions
The following data is based on the product molecular weight 379.46. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.64 mL | 13.18 mL | 26.35 mL |
5 mM | 0.53 mL | 2.64 mL | 5.27 mL |
10 mM | 0.26 mL | 1.32 mL | 2.64 mL |
50 mM | 0.05 mL | 0.26 mL | 0.53 mL |
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Product Datasheets
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References
References are publications that support the products' biological activity.
Bylund et al (1992) Pharmacological characteristics of α2-adrenergic receptors: comparison of pharmacologically defined subtypes with subtypes identified by molecular cloning. Mol.Pharmacol. 42 1 PMID: 1353247
Nelson and Taylor (1986) Spiroxatrine: a selective serotonin 1A receptor antagonist. Eur.J.Pharmacol. 124 207 PMID: 3720840
Schoeffter and Hoyer (1988) Centrally acting hypotensive agents with affinity for 5-HT1A binding sites inhibit forskolin-stimulated adenylate cyclase activity in calf hippocampus. Br.J.Pharmacol. 95 975 PMID: 3207999
Keywords: Spiroxatrine, supplier, Potent, α2C-adrenoceptor, alpha2C-adrenoceptor, alpah4c-adrenergic, a2c-adrenoceptor, a2c-adrenergic, antagonists, 5-HT1A, Receptors, Serotonin, Adrenergic, Alpha-2, Receptors, Tocris Bioscience