Brevilin A
CAS No. 16503-32-5
Brevilin A( —— )
Catalog No. M22858 CAS No. 16503-32-5
Brevilin A is a sesquiterpene lactone isolated from Centipeda minima, inhibits janus kinase activity and blocks STAT3 signaling in cancer cells with anti-tumor activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 203 | In Stock |
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| 10MG | 350 | In Stock |
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| 25MG | 579 | In Stock |
|
| 50MG | 797 | In Stock |
|
| 100MG | 1071 | In Stock |
|
| 500MG | 2187 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameBrevilin A
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NoteResearch use only, not for human use.
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Brief DescriptionBrevilin A is a sesquiterpene lactone isolated from Centipeda minima, inhibits janus kinase activity and blocks STAT3 signaling in cancer cells with anti-tumor activity.
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DescriptionBrevilin A is a sesquiterpene lactone isolated from Centipeda minima, inhibits janus kinase activity and blocks STAT3 signaling in cancer cells with anti-tumor activity. Brevilin A is a selective inhibitor of JAK-STAT signal pathway by attenuating the JAKs activity and blocking STAT3 signaling (IC50 = 10.6 μM) in Cancer Cells.Brevilin A induces apoptosis and autophagy via mitochondrial pathway and PI3K/AKT/mTOR inactivation in colon adenocarcinoma cell CT26.antitumourIn vitro activity against Giardia intestinalis was used for bioassay-guided fractionation of crude extracts from C. minima. The sesquiterpene lactone, Brevilin A was isolated and found to have antigiardial activity (IC50 = 16.1 μM) and was similarly active in vitro against Entamoeba histolytica (IC50 between 4.5 and 9 μM) and against Plasmodium falciparum (IC50 = 9.42 μM).
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In VitroCell Viability Assay Cell Line:A549R cells Concentration:1-20 μM Incubation Time:24 hours Result:Exhibited STAT3 signaling inhibition in a dose dependent manner with IC50 value of 10.6 μM.Cell Proliferation Assay Cell Line:CNE-2 cells Concentration:0-50 μM Incubation Time:24, 48, and 72 hours Result:Showed IC50 values in CNE-2 cells with treatment times of 24, 48, and 72 h of 7.93, 2.60, and 22.26 μM, respectively.Apoptosis Analysis Cell Line:DU145 and MDA-MB-468 cells Concentration:10 μM Incubation Time:24 and 48 hours Result:Decreased c-Myc and CyclinD1 after 24 h and 48 h treatment, increased cleaved PARP after 24 h treatment.Western Blot Analysis Cell Line:A549R cells Concentration:12.5 and 25 μM Incubation Time:24 hours Result:Inhibits STAT3 phosphorylation in A549R cells.
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In VivoAnimal Model:Male BALB/c nude mice injected with CNE-2 cellsDosage:10 and 20 mg/kg Administration:Oral gavage; 10 and 20 mg/kg; once daily; 16 days Result:Decreased average tumor volumes and weights treated with 20 mg/kg by 36.3% and 46.0%, respectively, compared to vehicle control.Inhibited the protein expression of p-AKT and p-STAT3 at both low and high doses.
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Synonyms——
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PathwayMicrobiology/Virology
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TargetAntifection
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RecptorAntifection|JAK|STAT
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Research Area——
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Indication——
Chemical Information
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CAS Number16503-32-5
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Formula Weight346.41
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Molecular FormulaC20H26O5
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Purity>98% (HPLC)
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SolubilityDMSO:100 mg/mL (288.67 mM; Need ultrasonic)
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SMILESC/C=C(C)\C(O[C@H]1[C@@]([C@@H]2C)([H])[C@@](OC2=O)([H])C[C@@H](C)[C@@]3([H])[C@]1(C(C=C3)=O)C)=O
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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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Ethyl coumarin-3-car...
Ethyl 3-coumarincarboxylate is a coumarin derivative.
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alpha-Terpineol
Terpineol possesses antifungal activity against Trichophyton mentagrophytes, it also exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria. α-Terpineol shows anticonvulsant, and anti-inflammatory activities, it inhibits the gene expression of the IL-6 receptor.
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Altenuene
Altenuene is a mycotoxin, it frequently occurs in food and feed items infested by fungi of the genus Alternaria. Altenuene demonstrates moderate activity against Staphylococcus aureus. Altenuene also exhibits cytotoxic activity against lung cancer cell line A549, breast cancer cell line MDA-MB-231 and pancreatic cancer cell line PANC-1.
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