Diproteverine HCl
CAS No. 69373-88-2
Diproteverine HCl( —— )
Catalog No. M36266 CAS No. 69373-88-2
Diproteverine HCl is a novel calcium antagonist with antianginal properties, antispasmodic and vasoactive.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 296 | Get Quote |
|
| 5MG | 409 | Get Quote |
|
| 10MG | 604 | Get Quote |
|
| 25MG | 908 | Get Quote |
|
| 50MG | 1251 | Get Quote |
|
| 100MG | 1647 | Get Quote |
|
| 500MG | 3312 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameDiproteverine HCl
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NoteResearch use only, not for human use.
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Brief DescriptionDiproteverine HCl is a novel calcium antagonist with antianginal properties, antispasmodic and vasoactive.
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DescriptionDiproteverine HCl is a novel calcium antagonist with antianginal properties, antispasmodic and vasoactive.
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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 Number69373-88-2
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Formula Weight462.02
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Molecular FormulaC26H36ClNO4
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Purity>98% (HPLC)
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Solubility——
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SMILESCl.N1=C(C=2C=C(OC(C)C)C(OC(C)C)=CC2CC1)CC3=CC=C(OCC)C(OCC)=C3
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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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Dantrolene sodium he...
Dantrolene is a postsynaptic muscle relaxant that lessens excitation-contraction coupling in muscle cells.
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alpha-L-Rhamnose
Addition of the Rhamnose-rich polysaccharide RROP-1 to normal human dermal fibroblasts (NHDFs) and human endothelial cells produced a dose-dependent stimulation of the calcium-signaling pathway inducing fast and transient increases in Ca2 influx and intracellular free Ca2 level.
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L-Phenylalanine-15N
L-Phenylalanine-15N ((S)-2-Amino-3-phenylpropionic acid-15N) is the 15N-labeled L-Phenylalanine. L-Phenylalanine ((S)-2-Amino-3-phenylpropionic acid) is an essential amino acid isolated from Escherichia coli . L-Phenylalanine is a α2δ subunit of voltage-dependent Ca + channels antagonist with a K i of 980 nM.
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