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Art. -Nr.: HY-A0022

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Azaphen

Name: Azaphen
Brand: MedChemExpress
SKU: HY-A0022
Availability: PreOrder

(Synonyms: Azafen; Pipofezin hydrochloride; Pipofezine hydrochloride)

1 Cited Publications

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Based on 1 publication(s) in Google Scholar

Azaphen (Azafen) is an orally active tricyclic antidepressant that inhibits the reuptake of serotonin and monoamines, regulates the 5-HT2c receptor, and exerts sedative, antidepressant and anxiolytic effects. Azaphen increases the bioavailability of serotonin in the synaptic cleft, does not block muscarinic receptors or affect monoamine oxidase activity, and binds to the human serotonin transporter via salt bridges, π-stacking, π-cation and hydrophobic interactions. Azaphen can be used in studies related to depression.

Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.

CAS. Nr.: 24853-80-3
Formel: C₁₆H₂₁Cl₂N₅O
Molecular Weight:370.28

Speicherung:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (277 KB)

Azaphen Chemical Structure

CAS. Nr.: 24853-80-3

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Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biologische Aktivität
- Beschreibung
- In Vitro
- In Vivo
Chemical Information
Publications (1)
Reinheit & Dokumentation
Verweise
Calculators
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Classifications
Bioz

Biologische Aktivität

Beschreibung

Alle 5-HT Receptor Isoform-spezifische Produkte anzeigen :

In Vitro

Azaphen (Azafen) (Less than 1 mg; 0.5 s exposure per frame, 2° s^-1 rotation rate, 120° total rotation angle) has its first atomic solid-state structure solved by MicroED at 0.82 Å resolution, revealing two inversion-related conformers with minimal conformational flexibility that supports binding to its target protein^[3].
Azaphen binds preferentially to the allosteric (S2) site of hSERT with minimal conformational change from its solid-state structure, stabilized by multiple key interactions including a salt bridge, pi-stacking, and pi-cation interactions^[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Azaphen (Azafen) (5-20 mg/kg; p.o.; single dose) exhibits pronounced antidepressant activity in the Porsolt behavioral despair test, with significant reductions in immobility duration at oral doses of 5, 10, and 20 mg/kg^[2].
Azaphen exhibits pronounced antidepressant activity in the Normura forced swimming test with significant reductions in depressive state duration^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

Mongrel albino rats (70-90 days old, 200-250 g, behavioral despair induced via Porsolt forced swimming test)^[2]
Dosage:

5 mg/kg; 10 mg/kg; 20 mg/kg
Administration:

p.o.; single dose
Result:

Significantly shortened the duration of immobility (depressive state) compared to control.

Related Protocols :

Protocol for Pharmacokinetic Study

Chemical Information

CAS. Nr. 24853-80-3
Molecular Weight 370.28
Formel C₁₆H₂₁Cl₂N₅O
SMILES

[H]Cl.[H]Cl.CN1C2=CC=CC=C2OC3=C1C=C(N4CCN(C)CC4)N=N3
Synonyms

Azafen; Pipofezin hydrochloride; Pipofezine hydrochloride
Structure Classification
- Others
Initial Source
- Animal
from the cadaveric material
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

Please store the product under the recommended conditions in the Certificate of Analysis.

Publications (1)

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Journal Impact Factor

Biochim Biophys Acta Gen Subj

5-Hydroxytryptamine activates a 5-HT/c-Myc/SLC6A4 signaling loop in non-small cell lung cancer. [Abstract]

2022 Apr;1866(4):130093. PMID: 35066124

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (277 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Imran M, et al. Study of various pyridazine and phthalazine drugs with diverse therapeutically and agrochemically activities. Russ J Bioorg Chem. 2020;46(5):745-767.

[2]. Aleeva GN, et al. Comparison of antidepressant effects of azafan, tianeptine, and paroxetine. Bulletin of experimental biology and medicine. 2009 Jul;148(1):54-6.

[3]. Lin J, et al. Uncovering the Elusive Structures and Mechanisms of Prevalent Antidepressants. Advanced therapeutics. 2024 Sep;7(9):2400117.

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Bioz

Azaphen

1 Cited Publications

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Biologische Aktivität
- Beschreibung
- In Vitro
- In Vivo
Chemical Information
Publications (1)
Reinheit & Dokumentation
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Azaphen

Publications Citing Use of MedChemExpress (MCE) Azaphen

Alle 5-HT Receptor Isoform-spezifische Produkte anzeigen