Azelnidipine
CAS No. 123524-52-7
Azelnidipine( CS 905 | RS 9054 )
Catalog No. M10941 CAS No. 123524-52-7
Azelnidipine is a dihydropyridine calcium channel blocker.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 54 | In Stock |
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| 2MG | 29 | In Stock |
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| 5MG | 42 | In Stock |
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| 10MG | 59 | In Stock |
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| 25MG | 105 | In Stock |
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| 50MG | 166 | In Stock |
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| 100MG | 269 | In Stock |
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| 200MG | 398 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameAzelnidipine
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NoteResearch use only, not for human use.
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Brief DescriptionAzelnidipine is a dihydropyridine calcium channel blocker.
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DescriptionAzelnidipine is a dihydropyridine calcium channel blocker.
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In Vitro——
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In Vivo——
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SynonymsCS 905 | RS 9054
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number123524-52-7
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Formula Weight582.65
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Molecular FormulaC33H34N4O6
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Purity>98% (HPLC)
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SolubilityDMSO: 117mg/ml (200.81 mM); Water: <1mg/ml; Ethanol: 7mg/ml (12.01 mM)
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SMILESO=C(C1=C(N)NC(C)=C(C(OC(C)C)=O)C1C2=CC=CC([N+]([O-])=O)=C2)OC3CN(C(C4=CC=CC=C4)C5=CC=CC=C5)C3
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Chemical Name3-(1-benzhydrylazetidin-3-yl) 5-isopropyl 2-amino-6-methyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
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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Amlodipine maleate
Amlodipine maleate (Amvaz) is an orally active dihydropyridine calcium channel blocker that inhibits calcium inward flow by blocking voltage-dependent L-type calcium channels.Amlodipine maleate is used in the study of hypertension and cancer.
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Imagabalin
Imagabalin (PD 0332334) is a novel ligand for the α2δ subunit of the voltage-dependent calcium channel (VDCC) with some selectivity for the α2δ1 subunit over α2δ2.
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Ziconotide Acetate ...
Ziconotide is an analgesic agent and has been used to treat neuropathic and non-neuropathic pain. Ziconotide acts by binding to N-type calcium channels situated on the terminal part of primary afferent neurons of the nociceptive pathway therefore reducing synaptic transmission with potent antinociceptive effects.
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