
Deoxypodophyllotoxin
CAS No. 19186-35-7
Deoxypodophyllotoxin( —— )
Catalog No. M22118 CAS No. 19186-35-7
Deoxypodophyllotoxin shows cytotoxic , antineoplastic, antitumor, insecticidal, anti-angiogenic, vascular disrupting, insecticidal, antiviral, and anti-inflammatory activities.Deoxypodophyllotoxin (DPT) induced both apoptosis and autophagy via production of mitochondrial reactive oxygen species (ROS).?
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 260 | In Stock |
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10MG | 447 | In Stock |
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25MG | 714 | In Stock |
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50MG | 972 | In Stock |
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100MG | 1305 | In Stock |
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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 NameDeoxypodophyllotoxin
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NoteResearch use only, not for human use.
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Brief DescriptionDeoxypodophyllotoxin shows cytotoxic , antineoplastic, antitumor, insecticidal, anti-angiogenic, vascular disrupting, insecticidal, antiviral, and anti-inflammatory activities.Deoxypodophyllotoxin (DPT) induced both apoptosis and autophagy via production of mitochondrial reactive oxygen species (ROS).?
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DescriptionDeoxypodophyllotoxin shows cytotoxic , antineoplastic, antitumor, insecticidal, anti-angiogenic, vascular disrupting, insecticidal, antiviral, and anti-inflammatory activities.Deoxypodophyllotoxin (DPT) induced both apoptosis and autophagy via production of mitochondrial reactive oxygen species (ROS).?DPT suppressed the PI3K/AKT/mTOR signaling cascades to lead autophagy process, resulting from conversion of light chain 3-I (LC3-I) into LC3-II and acidic vesicular organelles (AVOs) formation.?Even if DPT-induced ROS were occurred in both apoptosis and autophagy, inhibition of ROS generation enhanced cell viability.?Otherwise, 3-methyladeine (3-MA) impeding on autophagy accelerated an apoptotic response caused by DPT.?Therefore, these findings suggest that DPT triggers cytoprotective autophagy against cytotoxic apoptosis.
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In VitroDeoxypodophyllotoxin (25-75 nM; 6-48 hours) increases the percentage of early apoptotic cell populationfrom 2.05 to 5.62 and 18.49% for 24 h and 48 h, respectively.Deoxypodophyllotoxin (25-75 nM; 6-48 hours) treats SGC-7901 cells arrested in G2/M phase in time- and dose- dependent manners. Deoxypodophyllotoxin (25-75 nM; 6-48 hours) results in a remarkably time- and dose-dependent decrease in Cdc2 and Cdc25C expression levels and increases cyclin B1 within 6h, decreases PARP, Bcl-2 and caspase-3 activity. Apoptosis Analysis Cell Line:SGC-7901 cells Concentration:25, 50, 75 nM Incubation Time:6, 12, 24, 48 hours Result:Induced apoptosis in SGC-7901 Cells.Cell Cycle AnalysisCell Line:SGC-7901 cells Concentration:25, 50, 75 nM Incubation Time:6, 12, 24, 48 hours Result:Induced G2/M cell cycle arrest in SGC-7901 Cells Western Blot Analysis Cell Line:SGC-7901 cells Concentration:25, 50, 75 nM Incubation Time:6, 12, 24, 48 hoursResult:Altered the expression of cyclin B1, Cdc2,Cdc25C, p-PARP, Bcl-2 and p-caspase-3 proteins.
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In VivoDeoxypodophyllotoxin (intravenously injected; 5, 10, and 20 mg/kg; 3 times a week; 28 days) suppresses the tumors in a dose-dependent manner, the growth of tumors is inhibited by 22.19%, 47.91% and 50.93% with DPT at 5, 10 and 20 mg/kg, respectively. Animal Model:Xenograft model of gastric cancer in nude mice with SGC-7901 cells Dosage:5, 10, and 20 mg/kg Administration:Intravenously injected; 5, 10, and 20 mg/kg; 3 times a week; 28 days Result:Inhibited the growth of gastric cancer tumors.
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Synonyms——
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PathwayCytoskeleton/Cell Adhesion Molecules
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TargetMicrotubule/Tubulin
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Recptormicrotubule|Autophagy|Apoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number19186-35-7
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Formula Weight398.41
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Molecular FormulaC22H22O7
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (251.00 mM)
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SMILES[H][C@]12COC(=O)[C@]1([H])[C@H](c1cc(OC)c(OC)c(OC)c1)c1cc3OCOc3cc1C2
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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. Kim SH, et al. Deoxypodophyllotoxin induces cytoprotective autophagy against apoptosis via inhibition of PI3K/AKT/mTOR pathway in osteosarcoma U2OS cells. Pharmacol Rep. 2017 Oct;69(5):878-884.2. Deoxypodophyllotoxin exerts both anti-angiogenic and vascular disrupting effects.Int J Biochem Cell Biol. 2013 Aug;45(8):1710-9.
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