Description: 5-HT2 antagonist. Has moderate affinity for 5-HT6
Chemical Name: 1,2,3,4,10,14b-Hexahydro-2-methyldibenzo[c,f]pyrazino[1,2-a]azepine hydrochloride
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Non-selective 5-HT2 receptor antagonist (Ki values are 0.0080 and 0.0081 μM for human 5-HT2A and 5-HT2C receptors expressed in HEK293 cells respectively). Has moderate affinity for 5-HT6. Antidepressant.
Technical Data
M. Wt
300.83
Formula
C18H20N2.HCl
Storage
Store at RT
Purity
≥99% (HPLC)
CAS Number
21535-47-7
PubChem ID
68551
InChI Key
YNPFMWCWRVTGKJ-UHFFFAOYSA-N
Smiles
Cl.CN1CCN2C(C1)C1=CC=CC=C1CC1=C2C=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
water
3.01
10
Preparing Stock Solutions
The following data is based on the product molecular weight 300.83. 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
3.32 mL
16.62 mL
33.24 mL
5 mM
0.66 mL
3.32 mL
6.65 mL
10 mM
0.33 mL
1.66 mL
3.32 mL
50 mM
0.07 mL
0.33 mL
0.66 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Hoyeret al (1994) VII. International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (serotonin). Pharmacol.Rev. 46 157 PMID: 7938165
Leonard
(1982) On the mode of action of mianserin. Adv.Biochem.Psychopharmacol. 31 301 PMID: 6282060
Merck Index 12 6260 PMID:
Jensenet al (2013) Design, synthesis, and pharmacological characterization of N- and O-substituted 5,6,7,8-tetrahydro-4H-isoxazolo[4,5-dazepin-3-ol analogues: novel 5-HT2A/5-HT2C receptor agonists with pro-cognitive J.Med.Chem. 56 1211 PMID: 23301527