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Fenoverine
CAS No. 37561-27-6
Fenoverine( —— )
Catalog No. M35678 CAS No. 37561-27-6
Fenoverine (Spasmopriv) is a novel smooth muscle motor synchronizer with anti-spasmodic activity that inhibits fast and slow Ca2+ channel currents in a concentration-dependent manner and can be used to study gastrointestinal spasms.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 1398 | Get Quote |
|
| 50MG | 1822 | Get Quote |
|
| 100MG | 2250 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameFenoverine
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NoteResearch use only, not for human use.
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Brief DescriptionFenoverine (Spasmopriv) is a novel smooth muscle motor synchronizer with anti-spasmodic activity that inhibits fast and slow Ca2+ channel currents in a concentration-dependent manner and can be used to study gastrointestinal spasms.
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DescriptionFenoverine (Spasmopriv) is an antispasmodic agent and inhibits calcium channel currents. Fenoverine induces rhabdomyolysis.
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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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TargetCalcium Channel
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RecptorCalcium Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number37561-27-6
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Formula Weight459.56
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Molecular FormulaC26H25N3O3S
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C(N1C=2C=CC=CC2SC=3C=CC=CC31)CN4CCN(CC5=CC=C6OCOC6=C5)CC4
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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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Stugeron
Cinnarizine is a drug derivative of piperazine, and characterized as an antihistamine and a calcium channel blocker.
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Azumolene
Azumolene1.EU4093 (azumolene sodium) is a direct acting, skeletal muscle relaxant with structural similarities to dantrolene sodium in that the para-nitro phenyl group of dantrolene sodium is replaced by a para-bromo phenyl group.?2.?The effect of EU4093 on the twitch of the intact rat soleus preparation is nearly maximal at a dose of 20 mg kg-1.?
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Etripamil
Etripamil displays atrioventricular nodal conduction and prolongs atrioventricular nodal refractory periods by inhibiting calcium ion influx through the calcium slow channels in the atrioventricular node cells. Etripamil is an antagonist of short-acting L-type calcium-channel.
