Isolongifolene
CAS No. 1135-66-6
Isolongifolene ( (-)-Isolongifolene )
Catalog No. M23324 CAS No. 1135-66-6
Isolongifolene has antioxidant, anti-inflammatory, anticancer and neuroprotective properties.
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
5MG | 98 | In Stock |
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10MG | 146 | In Stock |
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25MG | 242 | In Stock |
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50MG | 358 | In Stock |
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100MG | Get Quote | In Stock |
|
200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameIsolongifolene
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NoteResearch use only, not for human use.
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Brief DescriptionIsolongifolene has antioxidant, anti-inflammatory, anticancer and neuroprotective properties.
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DescriptionIsolongifolene has antioxidant, anti-inflammatory, anticancer and neuroprotective properties. Isolongifolene is a tricyclic sesquiterpene isolated from Murraya koenigii. Isolongifolene attenuates Rotenone-induced oxidative stress, mitochondrial dysfunction and apoptosis through the regulation of P13K/AKT/GSK-3β signaling pathways.
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Synonyms(-)-Isolongifolene
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number1135-66-6
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Formula Weight204.4
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Molecular FormulaC15H24
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESCC1(C)[C@]23CC[C@](C3)([H])C(C)(C)C2=CCC1
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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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Cyclo(Pro-Val)
Cyclo(Pro-Val) shows cyctoxic, moderate antifungal and weak antitumor activities in vitro, it can inhibit the growth of Bacillus subtilis with the minimal inhibitory concentration (MIC) value of 0.8 g/L. Cyclo(Pro-Val) and cyclo(Pro-Tyr) are toxic to both suspension cells and seedlings of Pinus thunbergii, which may offer some clues to research the mechanism of pine wilt disease caused by pine wood nematode.
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Cinene
Limonene is a monoterpene in citrus peel oil. A popular disinfectant and food preservative.
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p-Cresol
p-Cresol (4-methylphenol) is a partially lipophilic moiety which strongly binds to plasma protein (close to 100%) under normal conditions. p-Cresol is metabolized through conjugation mainly sulphation and glucuronization but removal of the unconjugated p-cresol is at least in part via the urine.