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Organic heterocyclic compounds that consist of an azepine ring and a piperazine ring connected by a carbon-nitrogen bridge; piperazine is a six-membered ring with four carbon atoms and two nitrogen atoms at opposite positions in the ring.
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Mianserin (Bolvidon Norval Tolvon ORG GB-94 HCl Mianserin hydrochloride) is an potent antagonist of H1 histamine receptor and 5-HT serotonin receptors used for the treatment of depression
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Mianserin is a tetracyclic antidepressant-class research chemical that acts as an H1 histamine receptor inverse agonist. Supplied in measured small quantities for laboratory and analytical use, it is provided for research use only and is not intended for human therapeutic use.
High purity, typically ≈99.4%.
Tetracyclic antidepressant scaffold with H1 receptor inverse agonist activity.
Available in measured milligram quantities suitable for analytical and research applications.
Molecular formula C18H20N2 and molecular weight 264.36 g/mol.
Characterized and documented with supporting datasheet, COA, and spectral data for verification.
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(S)-Mirtazapine is the S(+)-enantiomer of mirtazapine, provided as a solid research chemical for laboratory and analytical use. For research use only; not for human or clinical use.
High purity: 99.76% (enantiomeric excess 98.35%).
Chemical formula: C17H19N3; molecular weight: 265.35 g/mol.
Appearance: off-white to light yellow powder.
Solubility: ≥100 mg/mL in DMSO; use newly opened DMSO due to hygroscopicity.
Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
Pack sizes suitable for small-scale research, including 10 mg quantities.
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(R)-Mirtazapine is the R-enantiomer of mirtazapine, described as a 5-HT3 receptor antagonist with reported antinociceptive activity. It is supplied as a high-purity solid research reagent intended for laboratory use.
High purity: 99.8%.
Chiral R-enantiomer with 5-HT3 receptor antagonist activity.
Chemical formula C17H19N3; molecular weight 265.35 g·mol⁻¹.
CAS number 61364-37-2 for substance identification.
Supplied as a solid powder suitable for analytical and preclinical research.
Storage: powder at -20°C (3 years) or 4°C (2 years); in solvent at -80°C (6 months).
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(S)-Mirtazapine ((S)-Org3770) is an S(+)-enantiomer of Mirtazapine, exhibiting pronociceptive properties within an animal model of acute thermal nociception. It functions as a stereoselective 5-HT2 receptor antagonist and undergoes metabolism by CYP2D6 and CYP1A2.
It is an S(+)-enantiomer of Mirtazapine.
It has pronociceptive properties in an animal model of acute thermal nociception.
It is a stereoselective 5-HT2 receptor antagonist.
It is metabolized by CYP2D6 and CYP1A2.
The molecular weight is 265.35.
The chemical formula is C17H19N3.
It appears as a solid.
The color ranges from off-white to light yellow.
The purity is 99.76%.
The enantiomeric excess is 98.35%.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More