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Fuziline
CAS No. 80665-72-1
Fuziline( —— )
Catalog No. M20295 CAS No. 80665-72-1
Fuziline shows significant insecticidal activity against Nilaparvata legen and Aphis medicagini. Fuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 72 | In Stock |
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| 2MG | 35 | In Stock |
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| 5MG | 55 | In Stock |
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| 10MG | 89 | In Stock |
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| 25MG | 149 | In Stock |
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| 50MG | 216 | In Stock |
|
| 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 NameFuziline
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NoteResearch use only, not for human use.
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Brief DescriptionFuziline shows significant insecticidal activity against Nilaparvata legen and Aphis medicagini. Fuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.
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DescriptionFuziline shows significant insecticidal activity against Nilaparvata legen and Aphis medicagini. Fuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.
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In VitroFuziline shows activity against pentobarbital sodiuminduced cardiomyocytes damage by obviously recovering beating rhythm and increasing the cell viability.
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In VivoFuziline exhibits the mean half-life of 5.93 hours, 6.13 hours and 5.12?hours for 14?mg/kg, 2 4?mg/kg and 4?mg/kg, respectively, by oral administration in rat.
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Synonyms——
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PathwayMicrobiology/Virology
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TargetAntifection
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RecptorAntifection
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Research Area——
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Indication——
Chemical Information
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CAS Number80665-72-1
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Formula Weight453.6
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Molecular FormulaC24H39NO7
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (220.47 mM)
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SMILES[H][C@]12C[C@]3([H])[C@]([H])([C@H]1O)[C@@](O)(C1[C@H](OC)[C@@]4([H])[C@]33[C@@H]1N(CC)C[C@]4(COC)CC[C@@H]3O)[C@@H](O)[C@@H]2OC
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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
1.Liang X Cheng P Xiao-Fang X et al. Alkaloids Isolated from the Lateral Root of Aconitum carmichaelii[J]. Molecules 2012 17(8):9939-9946.
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