85650-52-8
85650-52-8 structure
- Name: Mirtazapine
- Chemical Name: Mirtazapine
- CAS Number: 85650-52-8
- Molecular Formula: C17H19N3
- Molecular Weight: 265.353
- Catalog: Biochemical Inhibitor Neuronal Signaling 5-HT Receptor Antagonist
- Create Date: 2018-09-08 11:52:06
- Modify Date: 2026-07-01 19:33:28
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Mirtazapine is a potent tetracyclic antidepressant.Target: 5-HT ReceptorMirtazapine, the novel antidepressant, has a dual mode of action. It is a noradrenergic and specific serotonergic antidepressant (NaSSA) that acts by antagonizing the adrenergic alpha2-autoreceptors and alpha2-heteroreceptors as well as by blocking 5-HT2 and 5-HT3 receptors [1].Mirtazapine appears to have a substantial ameliorating effect on hot flushes and perspiration bouts. It is postulated that the 5-HT(2A) blocking properties of mirtazapine is accounted in the symptomatic relief of hot flushes [2]. After 4-24 weeks of treatment, mirtazapine induced downregulation of platelet alpha(2A)-adrenoceptors (up to 34%) and Galphai proteins (up to 28%), and the upregulation of GRK 2 (up to 30%). Treatment with mirtazapine reversed this abnormality and induced downregulation of alpha(2A)-adrenoceptor/Galphai complex [3].
| Name | Mirtazapine |
|---|---|
| Synonyms |
1,2,3,4,10,14B-HEXAHYDRO-2-METHYLPYRAZINO[2,1-A]PYRIDO[2,3-C]BENZAZINE
Zispin Mirtazapine, >= Mirtazapine, 10 mM in DMSO Mirtazapine, alpha2, 5-HT2, 5-HT3 antagonist Remeron Mirtazapine-d7 5-Methyl-2,5,19-triazatetracyclo[13.4.0.0^{2,7}.0^{8,13}]nonadeca-1,8,10,12,15,17-hexaene Mirtazapine //BP Mirtazapine(Org3770) 2-Methyl-1,2,3,4,10,14b-hexahydrobenzo[c]pyrazino[1,2-a]pyrido[3,2-f]azepine REMERON MIRTAZAPINE ANHYDRUOS Pyrazino[2,1-a]pyrido[2,3-c]benzazine Mirtazapine, 1mg/ml in Methanol ade Mirtazapine API 6-Azamianserin|||Org MIRTAZAPINE Mirtazapine - Bio-X UNII:A051Q2099Q Mirtazapine CRS Mirtazapine (ReMeron, Avanza) 2-Methyl-1,2,3,4,10,14b-hexahydropyrazino[2,1-a]pyrido[2,3-c][2]benzazepine MFCD00865427 Mirtazapine 5-HT Rector 1,2,3,4,10,14B-HEXAHYDRO-2-METHYLPYRAZINO[2.1-A]PYRIDO[2.3-C][2]BENZAZEPINE Mirtazapine Anhydrous (rs)-1,2,3,4,10,14b-hexahydro-2-methylpyrazino-[2,1-a]pyrido[2,3-c]benzazine Mirtazapine 1.0 mg/ml in Methanol 1,2,3,4,10,14B-HEXAHYDRO-2-METHYLPYRAZINO[2,1-A]PYRIDO[2,3-C][2]BENZAZEPINE ZISPIN ORG-3770 MIRTAZINE Mirtazapine> Mirtazapine anhydrous substance Mirtazanine (14bR)-2-methyl-1,2,3,4,10,14b-hexahydropyrazino[2,1-a]pyrido[2,3-c][2]benzazepine Mirtazapine (CRM) Mirtazapin MirtazapineQ: What is Mirtazapine Q: What is the CAS Number of Mirtazapine Q: What is the storage condition of Mirtazapine Q: What e the applications of Mirtazapine Mirtazapine dihydrochloride salt Mirtazapine in methanol MIRTAZANINE Mirtazapine-13C D3Q: What is Mirtazapine-13C D3 Q: What is the CAS Number of Mirtazapine-13C D3 Q: What is the storage condition of Mirtazapine-13C D3 Q: What e the applications of Mirtazapine-13C D3 Mirtazapine 13C, D3 MIRTAZEPINE Mirtazapine for system suitability CRS Avanza EINECS 288-060-6 |
| Description | Mirtazapine is a potent tetracyclic antidepressant.Target: 5-HT ReceptorMirtazapine, the novel antidepressant, has a dual mode of action. It is a noradrenergic and specific serotonergic antidepressant (NaSSA) that acts by antagonizing the adrenergic alpha2-autoreceptors and alpha2-heteroreceptors as well as by blocking 5-HT2 and 5-HT3 receptors [1].Mirtazapine appears to have a substantial ameliorating effect on hot flushes and perspiration bouts. It is postulated that the 5-HT(2A) blocking properties of mirtazapine is accounted in the symptomatic relief of hot flushes [2]. After 4-24 weeks of treatment, mirtazapine induced downregulation of platelet alpha(2A)-adrenoceptors (up to 34%) and Galphai proteins (up to 28%), and the upregulation of GRK 2 (up to 30%). Treatment with mirtazapine reversed this abnormality and induced downregulation of alpha(2A)-adrenoceptor/Galphai complex [3]. |
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| Related Catalog | |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 432.4±45.0 °C at 760 mmHg |
| Melting Point | 114-116ºC |
| Molecular Formula | C17H19N3 |
| Molecular Weight | 265.353 |
| Flash Point | 215.3±28.7 °C |
| Exact Mass | 265.157898 |
| PSA | 19.37000 |
| LogP | 2.75 |
| Vapour Pressure | 0.0±1.0 mmHg at 25°C |
| Index of Refraction | 1.668 |
| Storage condition | Store at RT |
| Water Solubility | DMSO: ~8 mg/mL, soluble |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302-H336 |
| Precautionary Statements | P301 + P312 + P330 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
| Hazard Codes | Xn |
| Risk Phrases | 22 |
| Safety Phrases | S22-S24/25 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2933990090 |
|
~94%
85650-52-8 |
| Literature: Singer, Claude; Liberman, Anita; Finkelstein, Nina Patent: US2001/51718 A1, 2001 ; Title/Abstract Full Text Show Details Singer, Claude; Liberman, Anita; Finkelstein, Nina Patent: US2003/69417 A1, 2003 ; |
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85650-52-8 |
| Literature: N.V. ORGANON Patent: WO2008/125578 A2, 2008 ; Location in patent: Page/Page column 16 ; |
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~55%
85650-52-8 |
| Literature: N.V. Organon Patent: US2008/255349 A1, 2008 ; Location in patent: Page/Page column 9 ; |
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| Literature: WO2008/125577 A1, ; Page/Page column 22 ; |
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| Literature: Organic Preparations and Procedures International, , vol. 39, # 4 p. 399 - 402 |
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85650-52-8 |
| Literature: Organic Preparations and Procedures International, , vol. 39, # 4 p. 399 - 402 |
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85650-52-8 |
| Literature: Organic Preparations and Procedures International, , vol. 39, # 4 p. 399 - 402 |
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85650-52-8 |
| Literature: Organic Preparations and Procedures International, , vol. 39, # 4 p. 399 - 402 |
| Precursor 7 | |
|---|---|
| DownStream 3 | |
![()-1,2,3,4,10,14b-hexahydro-2-methylpyrazino[2,1-a]pyrido[2,3-c][2]benzazepine maleate (1:1) structure](https://image.chemsrc.com/caspic/075/85650-53-9.png)
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |