Piperazinoazepines
Mianserin hydrochloride
CAS: 21535-47-7 Molecular Formula: C18H21ClN2 Molecular Weight (g/mol): 300.83 MDL Number: MFCD00055072 InChI Key: YNPFMWCWRVTGKJ-UHFFFAOYNA-N Synonym: mianserin hydrochloride,mianserine hydrochloride,mianserin hcl,athymil,bolvidon,tolvon,tolvin,org gb 94,lerivon PubChem CID: 68551 ChEBI: CHEBI:31843 IUPAC Name: hydrogen 5-methyl-2,5-diazatetracyclo[13.4.0.0²,⁷.0⁸,¹³]nonadeca-1(19),8,10,12,15,17-hexaene chloride SMILES: [H+].[Cl-].CN1CCN2C(C1)C1=CC=CC=C1CC1=CC=CC=C21
Mirtazapine, 98%
CAS: 85650-52-8 Molecular Formula: C17H19N3 Molecular Weight (g/mol): 265.35 InChI Key: RONZAEMNMFQXRA-UHFFFAOYSA-N Synonym: mirtazapine,remeron,mepirzepine,remergil,zispin,remergon,rexer,6-azamianserin,remeron soltab,mepirzapin PubChem CID: 4205 ChEBI: CHEBI:6950 SMILES: CN1CCN2C(C1)C3=CC=CC=C3CC4=C2N=CC=C4
Mianserin Hydrochloride 98.0+%, TCI America™
CAS: 21535-47-7 Molecular Formula: C18H21ClN2 Molecular Weight (g/mol): 300.83 MDL Number: MFCD00055072 InChI Key: YNPFMWCWRVTGKJ-UHFFFAOYNA-N Synonym: mianserin hydrochloride,mianserine hydrochloride,mianserin hcl,athymil,bolvidon,tolvon,tolvin,org gb 94,lerivon PubChem CID: 68551 ChEBI: CHEBI:31843 IUPAC Name: hydrogen 5-methyl-2,5-diazatetracyclo[13.4.0.0²,⁷.0⁸,¹³]nonadeca-1(19),8,10,12,15,17-hexaene chloride SMILES: [H+].[Cl-].CN1CCN2C(C1)C1=CC=CC=C1CC1=CC=CC=C21
Mirtazapine 98.0+%, TCI America™
CAS: 85650-52-8 Molecular Formula: C17H19N3 Molecular Weight (g/mol): 265.36 MDL Number: MFCD00865427 InChI Key: RONZAEMNMFQXRA-UHFFFAOYSA-N Synonym: mirtazapine,remeron,mepirzepine,remergil,zispin,remergon,rexer,6-azamianserin,remeron soltab,mepirzapin PubChem CID: 4205 ChEBI: CHEBI:6950 SMILES: CN1CCN2C(C1)C3=CC=CC=C3CC4=C2N=CC=C4
Apexbio Technology LLC Mianserin HCl 21535-47-7 100mg
Mianserin HCl (CAS 21535-47-7) is a small molecule that functions as a non-selective antagonist at 5-hydroxytryptamine (5-HT) 2 receptor subtypes and exhibits moderate affinity for 5-HT6 receptors Through its antagonistic activity at these serotonergic receptors Mianserin HCl modulates neurotransmission pathways implicated in mood regulation The compound is commonly utilized in neuropharmacological studies to investigate serotonergic signaling and has established utility as an antidepressant agent in clinical research
Apexbio Technology LLC Mirtazapine 85650-52-8 10mM (in 1mL DMSO)
Mirtazapine is a small-molecule antagonist targeting central presynaptic 2-adrenergic receptors as well as serotonin 5-HT2 and 5-HT3 receptors and central histamine H1 receptors It is designed to modulate monoaminergic neurotransmission thereby affecting mood regulation pathways Mirtazapine exerts its biological activity primarily through selective antagonism of central presynaptic 2-adrenergic receptors inducing increased synaptic release of norepinephrine and serotonin It also antagonizes serotonin 5-HT2 and 5-HT3 receptors Based on these pharmacological properties mirtazapine holds research potential in the fields of neuroscience and psychopharmacology particularly for studies involving depressive disorders anxiety conditions and mood regulation
TARGETMOL CHEMICALS INC R-Mirtazapine 5MG
Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. (R)-Mirtazapine ((R)-Org3770) is the R(-)-enantiomer of Mirtazapine, exhibiting anti-injury sensory properties in an animal model of acute thermal hyperalgesia. It functions as a 5-HT3 receptor antagonist and serves as a potential analgesic. Purity 99.75%
Medchemexpress LLC Mirtazapine | 85650-52-8 | >99.9% | 265.36 | 100 MG
Mirtazapine | 85650-52-8 | >99.9% | 265.36 | 100 MG
Selleck Chemical LLC Mirtazapine S2016-50mg
Mirtazapine (Org3770 6-Azamianserin) is an adrenergic and seroton receptor antagonist used to treat depression
Selleck Chemical LLC Mianserin HCl S1382-50mg
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
Sigma Aldrich Fine Chemicals Biosciences Timolol for system suitabi
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
Medchemexpress LLC Mirtazapine | 85650-52-8 | 99.95% | 50 MG
Mirtazapine (Standard) is the analytical standard of Mirtazapine, intended for research and analytical applications. It is a potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent, acting as a 5-HT2, 5-HT3, histamine H1 receptor, and α2-adrenoceptor antagonist. This compound is commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Analytical standard for Mirtazapine
- Intended for research and analytical applications
- Potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent
- Acts as a 5-HT2, 5-HT3, histamine H1 receptor, and α2-adrenoceptor antagonist
- Used in qualitative, quantitative and methodological research experiments
- Suitable for HPLC, GC, and MS applications
Medchemexpress LLC Mirtazapine | 85650-52-8 | 99.9% | 1 ML
Mirtazapine is a potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent. It functions as a 5-HT2, 5-HT3, histamine H1 receptor, and α2-adrenoceptor antagonist. Mirtazapine enhances the release of norepinephrine and 5-HT1A-mediated serotonergic transmission.
- Antagonizes adrenergic α2-autoreceptors and α2-heteroreceptors
- Blocks 5-HT2 and 5-HT3 receptors
- Enhances norepinephrine release
- Enhances 5-HT1A-mediated serotonergic transmission
- Reduces activation-induced release of cytokine/chemokine mediators from human CD14+ monocytes
- Inhibits hepatic macrophage/monocyte activation and decreases pro-inflammatory cytokine and chemokine production
Medchemexpress LLC Mianserin | 24219-97-4 | 99.4% | 264.36 g/mol | C18H20N2 | 10 MG
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.
Medchemexpress LLC Mianserin | 24219-97-4 | 99.42% | 25 MG
Mianserin is an orally active H1 receptor antagonist that can also activate κ-opioid and octopamine receptors. It increases ERK1/2 and CREB phosphorylation and antagonizes full κ-opioid agonist and Dynorphin A-induced MAPK phosphorylation. Mianserin modulates social and exploratory behavior and raises electroconvulsive thresholds. It is used in the research of neurological diseases such as depression and epilepsy.
- Orally active H1 receptor antagonist
- Activates κ-opioid receptor and octopamine receptor
- Increases ERK1/2 and CREB phosphorylation
- Antagonizes full κ-opioid agonist and Dynorphin A-induced MAPK phosphorylation
- Modulates social and exploratory behavior
- Raises electroconvulsive thresholds
- Useful for research into neurological diseases like depression and epilepsy