Levamlodipine
CAS No. 103129-82-4
Levamlodipine( Levamlodipine | S-Amlodipine | )
Catalog No. M10152 CAS No. 103129-82-4
Amlodipine is a synthetic dihydropyridine and a calcium channel blocker with antihypertensive and antianginal properties.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 36 | In Stock |
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| 50MG | 51 | In Stock |
|
| 100MG | 71 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 176 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameLevamlodipine
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NoteResearch use only, not for human use.
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Brief DescriptionAmlodipine is a synthetic dihydropyridine and a calcium channel blocker with antihypertensive and antianginal properties.
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DescriptionAmlodipine is a synthetic dihydropyridine and a calcium channel blocker with antihypertensive and antianginal properties. Amlodipine inhibits the influx of extracellular calcium ions into myocardial and peripheral vascular smooth muscle cells, thereby preventing vascular and myocardial contraction. This results in a dilatation of the main coronary and systemic arteries, decreased myocardial contractility, increased blood flow and oxygen delivery to the myocardial tissue, and decreased total peripheral resistance. This agent may also modulate multi-drug response (MDR) activity through inhibition of the p-glycoprotein efflux pump.
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In Vitro——
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In Vivo——
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SynonymsLevamlodipine | S-Amlodipine |
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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 Number103129-82-4
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Formula Weight408.88
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Molecular FormulaC20H25N2O5Cl
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM
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SMILESO=C(C1=C(COCCN)NC(C)=C(C(OC)=O)[C@@H]1C2=CC=CC=C2Cl)OCC
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Chemical Name3-ethyl 5-methyl (S)-2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methyl-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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ω-Conotoxin GVIA
Peptide neurotoxin; selectively and reversibly blocks N-type calcium channels (IC50 = 0.15 nM). Reduces (RS)-3,5-DHPG -induced long term depression in vivo.
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2-Nitrobenzoic acid
2-Nitrobenzoic acid (o-Nitrobenzoic acid) is a antiproliferation agent. 2-Nitrobenzoic acid shows IC50 of 8.3 μM to jurkat cell line expressing T type calcium channel alpha 1H or its splice variant delta 25.
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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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