Biological Activity
Antidepressant agent; potent 5-HT2, 5-HT3 and histamine H1 receptor antagonist and moderately potent α2-adrenoceptor antagonist (pKi values are 8.05, ~ 8.1, 9.3 and 6.95 respectively). Enhances noradrenalin (NA) release in rat brain via inhibition of α2-adrenergic autoreceptors and displays only weak affinity for monoamine transporters (pKi values are 5.6, < 5 and < 5.1 for inhibition of NA, dopamine and 5-HT uptake respectively). Increases hippocampal NA and 5-HT levels in rats following systemic administration in vivo.
Compound Libraries
Mirtazapine is also offered as part of the Tocriscreen Plus and Tocriscreen Library of FDA-Approved Compounds. Find out more about compound libraries available from Tocris.
Technical Data
M. Wt | 265.36 |
Formula | C17H19N3 |
Storage | Store at RT |
Purity | ≥99% (HPLC) |
CAS Number | 85650-52-8 |
PubChem ID | 4205 |
InChI Key | RONZAEMNMFQXRA-UHFFFAOYSA-N |
Smiles | CN1CCN2C(C1)C1=CC=CC=C1CC1=C2N=CC=C1 |
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 | 5.31 | 20 | |
ethanol | 13.27 | 50 |
Preparing Stock Solutions
The following data is based on the product molecular weight 265.36. 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 | 3.77 mL | 18.84 mL | 37.68 mL |
5 mM | 0.75 mL | 3.77 mL | 7.54 mL |
10 mM | 0.38 mL | 1.88 mL | 3.77 mL |
50 mM | 0.08 mL | 0.38 mL | 0.75 mL |
Molarity Calculator
Reconstitution Calculator
Dilution Calculator
Product Datasheets
References
References are publications that support the products' biological activity.
de Boer et al (1988) Neurochemical and autonomic pharmacological profiles of the 6-aza-analogue of mianserin, ORG 3770 and its enantiomers. Neuropharmacology 27 399 PMID: 3419539
Kooyman et al (1994) Interaction between enantiomers of mianserin and ORG3770 at 5-HT3 receptors in cultured mouse neuroblastoma cells. Neuropharmacology 33 501 PMID: 7984289
de Boer et al (1996) Differences in modulation of noradrenergic and serotonergic transmission by the alpha-2 adrenoceptor antagonists, mirtazepine, mianserin and idazoxan. J.Pharmacol.Exp.Ther. 277 852 PMID: 8627567
Keywords: Mirtazapine, supplier, Potent, 5-HT3, antagonists, 5-HT2, H1, α2-adrenoceptor, alpha2-adrenoceptor, a2-adrenoceptor, α2-Adrenergic, alpha2-Adrenergic, a2-adrenergic, Antidepressant, Serotonin, Receptors, Non-Selective, Histamine, histaminergic, Org3770, Org, 3770, 6-Azamianserin, Non-selective, 5-HT2, 5-HT3, Receptors, Histamine, H1, Receptors, Adrenergic, Alpha-2, Receptors, Non-selective, 5-HT2, Tocris Bioscience