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Barnidipine(b)
CAS No. 104713-75-9
Barnidipine(b)( Mepirodipine | YM-09730-5(Free base) )
Catalog No. M20821 CAS No. 104713-75-9
Barnidipine is a 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 | 93 | In Stock |
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| 2MG | 49 | In Stock |
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| 5MG | 78 | In Stock |
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| 10MG | 119 | In Stock |
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| 25MG | 231 | In Stock |
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| 50MG | 338 | In Stock |
|
| 100MG | 509 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameBarnidipine(b)
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NoteResearch use only, not for human use.
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Brief DescriptionBarnidipine is a calcium channel blocker.
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DescriptionBarnidipine is a calcium channel blocker.
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In Vitro——
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In Vivo——
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SynonymsMepirodipine | YM-09730-5(Free base)
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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 Number104713-75-9
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Formula Weight491.54
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Molecular FormulaC27H29N3O6?
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Purity>98% (HPLC)
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Solubility——
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SMILESCOC(=O)C1=C(C)NC(C)=C(C(=O)O[C@H]2CCN(Cc3ccccc3)C2)[C@H]1c1cccc([N+](=O)[O-])c1
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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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SR33805
SR33805 is a potent antagonist of Ca2+ channel(EC50s of 4.1 nM and 33 nM in depolarized and polarized conditions, respectively)Acute treatment with SR33805 restored the MI-altered cell shortening without affecting the Ca(2+) transient amplitude, suggesting an increase of myofilament Ca(2+) sensitivity in MI myocytes.?
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HUP30
HUP30 is a potent vasodilating agent. HUP30 can stimulate soluble guanylyl cyclase, activate K+ channels, and block extracellular Ca2+ influx.
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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.
