Azaphen dihydrochloride monohydrate
CAS No. 63302-99-8
Azaphen dihydrochloride monohydrate( —— )
Catalog No. M35587 CAS No. 63302-99-8
Azaphen dihydrochloride monohydrate (Pipofezin dihydrochloride monohydrate) is a serotonin reuptake inhibitor with antidepressant activity and sedative effects, which can be used to study neurological diseases.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 35 | In Stock |
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| 25MG | 56 | In Stock |
|
| 50MG | 80 | In Stock |
|
| 100MG | 117 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameAzaphen dihydrochloride monohydrate
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NoteResearch use only, not for human use.
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Brief DescriptionAzaphen dihydrochloride monohydrate (Pipofezin dihydrochloride monohydrate) is a serotonin reuptake inhibitor with antidepressant activity and sedative effects, which can be used to study neurological diseases.
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DescriptionPipofezine(Azafen or Azaphen) is a potent inhibitor of the reuptake of serotonin. IC50 Value: Target: SSRIs Pipofezine is a tricyclic antidepressant (TCA) approved in Russia for the treatment ofdepression.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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Target5-HT Receptor
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Recptor5-HT Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number63302-99-8
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Formula Weight388.29
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Molecular FormulaC16H23Cl2N5O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : ≥ 100 mg/mL (257.54 mM) DMSO : 1 mg/mL (2.58 mM; Ultrasonic )
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SMILESCN1C2=C(C=CC=C2)OC3=NN=C(N4CCN(CC4)C)C=C31.Cl.O.Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Tropanserin
Tropanserin (MDL 72422) is a 5-hydroxytryptamine receptor antagonist that inhibits 5-HT3 receptor activity.Tropanserin has anxiolytic activity and is used to treat depression and cognitive disorders.
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Adatanserin hydrochl...
Adatanserin hydrochloride (WY50324 hydrochloride) is a novel 5-HT(1A)/5-HT(2) receptor ligand with potential neuroprotective effects and inhibition of ischemic efflux of endogenous amino acids, which can be used in the study of depression and anxiety disorders.
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ST1936
ST1936 (ST 1936 oxalate) is a selective and highly potent 5-HT6 receptor agonist that inhibits human 5-HT6, 5-HT7 and 5-HT2B receptors by fully activating cloned human 5-HT6 receptors.
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