Lappaconite HBr
CAS No. 97792-45-5
Lappaconite HBr( Allapinin | Lappaconiti hydrobromidum )
Catalog No. M19298 CAS No. 97792-45-5
Lappaconite Hydrobromide is a kind of alkaloid extracted from Aconitum sinomontanum Nakai. It has anti-inflammatory effects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 48 | In Stock |
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| 50MG | 47 | In Stock |
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| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameLappaconite HBr
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NoteResearch use only, not for human use.
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Brief DescriptionLappaconite Hydrobromide is a kind of alkaloid extracted from Aconitum sinomontanum Nakai. It has anti-inflammatory effects.
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DescriptionAllapinin is a potential antitumor agent agent that induces HL-60 differentiation and apoptosis with analgesic activity as well.
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In Vitro——
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In Vivo——
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SynonymsAllapinin | Lappaconiti hydrobromidum
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PathwayEndocrinology/Hormones
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TargetAChR
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RecptorOthers
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number97792-45-5
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Formula Weight665.61
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Molecular FormulaC32H44N2O8·HBr
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Purity>98% (HPLC)
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Solubility——
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SMILESCCN1C[C@@]2(CC[C@@H]([C@@]34[C@@H]2C[C@@H](C13)[C@]1(C[C@@H]([C@H]2C[C@@H]4[C@@]1([C@H]2OC)O)OC)O)OC)OC(=O)c1ccccc1NC(=O)C.Br
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Chemical Name(3S,6S,6aS,7S,7aS,8S,9R,10S,11aS,12S,12aR,14S)-1-ethyl-7a,11a-dihydroxy-6,8,10-trimethoxydodecahydro-2H-3,6a,12-(epiethane[1,1,2]triyl)-7,9-methanonaphtho[2,3-b]azocin-3(4H)-yl 2-acetamidobenzoate hydrobromide
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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2-Chloroadenosine
2-Chloroadenosine (CADO) is a metabolically stable analog of adenosine that binds to adenosine A1 A2A and A3 receptors( Ki:300 80 and 1900 nM respectively).
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Nicotine Ditartrate
(?)-Nicotine is the dominant form of the natural alkaloid nicotine. It acts as an agonist of neuronal nicotinic acetylcholine receptors (nAChRs) and possesses addictive and teratogenic properties. (?)-(S)-Nicotine is significantly more active at binding nAChRs compared to the (+)-(R) antipode thus nicotine is typically synthesized as (?)-(S)-nicotine with only 0.2-1% of the (+)-(R) isomer present.
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Diphenidol hydrochlo...
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