Withaferin A | NFkB and angiogenesis inhibitor
NMR (Conforms)
Available Options
| Size: | Price | Quantity | |
|---|---|---|---|
| 1 mg | $65.00 | ||
| 5 mg | $200.00 |
Withaferin A (5119-48-2) displays potent antiangiogenesis activity inhibiting endothelial cell sprouting in vitro (IC50 = 12 nM) and in vivo.1 Potently inhibits NF-κB activation by preventing TNFα-induced activation of IKKβ.2 Covalently binds to the intermediate filament protein, vimentin3 inducing its disassembly and serine 56 phosphorylation4. Inhibits reactive gliosis and blocks TNFα-mediated neuronal apoptosis in in vivo models.5
References/Citations:
1) Mohan et al. (2004), Withaferin A is a potent inhibitor of angiogenesis; Angiogenesis, 7 115
2) Kaileh et al. (2007), Withaferin A strongly elicits IkappaB kinase beta hyperphosphorylation concomitant with inhibition of its kinase activity; J. Biol. Chem., 282 4253
3) Bargagna-Mohan et al. (2007), The tumor inhibitor and antiangiogenic agent withaferin A targets the intermediate filament protein vimentin; Chem. Biol., 14 623
4) Thaiparambil et al. (2011), Withaferin A inhibits breast cancer invasion and metastasis at sub-cytotoxic doses by inducing vimentin disassembly and serine 56 phosphorylation; Int. J. Cancer, 129 2744
5) Livne-Bar et al. (2016), Pharmacologic inhibition of reactive gliosis blocks TNF-α-mediated neuronal apoptosis; Cell Death Dis., 7 e2386
NMR (Conforms)
Safety Data Sheet:
Product Data Sheet:
Materials provided by Focus Biomolecules are for laboratory research use only and are not intended for human or veterinary applications. Please note that we do not sell to individuals and that all orders placed by non-research organizations will incur a $20 restocking/refund fee
Withaferin A (5119-48-2) displays potent antiangiogenesis activity inhibiting endothelial cell sprouting in vitro (IC50 = 12 nM) and in vivo.1 Potently inhibits NF-κB activation by preventing TNFα-induced activation of IKKβ.2 Covalently binds to the intermediate filament protein, vimentin3 inducing its disassembly and serine 56 phosphorylation4. Inhibits reactive gliosis and blocks TNFα-mediated neuronal apoptosis in in vivo models.5
References/Citations:
1) Mohan et al. (2004), Withaferin A is a potent inhibitor of angiogenesis; Angiogenesis, 7 115
2) Kaileh et al. (2007), Withaferin A strongly elicits IkappaB kinase beta hyperphosphorylation concomitant with inhibition of its kinase activity; J. Biol. Chem., 282 4253
3) Bargagna-Mohan et al. (2007), The tumor inhibitor and antiangiogenic agent withaferin A targets the intermediate filament protein vimentin; Chem. Biol., 14 623
4) Thaiparambil et al. (2011), Withaferin A inhibits breast cancer invasion and metastasis at sub-cytotoxic doses by inducing vimentin disassembly and serine 56 phosphorylation; Int. J. Cancer, 129 2744
5) Livne-Bar et al. (2016), Pharmacologic inhibition of reactive gliosis blocks TNF-α-mediated neuronal apoptosis; Cell Death Dis., 7 e2386
Related products
-
Thalidomide | E3 UB ligase inhibitor
From $50.00CAS:50-35-1Catalog Number:10-1115Activity:E3 UB ligase inhibitorChemical Name:N-(2,6-Dioxo-3-piperidinyl)phthalimide, racemicMolecular Weight:258.25Molecular Formula:C13H10N2O4Solubility:Soluble in DMSO (up to 5 mg/ml).Physical Properties:White solidPurity:98% by TLC
NMR (Conforms)Storage Temperature:RTStability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month.Shipping Code:RT -
Herbimycin A | HSP90 Inhibitor
From $90.00CAS:70563-58-5Catalog Number:10-2567Activity:HSP90 InhibitorChemical Name:(15R)-17-Demethoxy-15 methoxy-11-O-methyl-geldanamycinMolecular Weight:574.68Molecular Formula:C30H42N2O9Solubility:Soluble in DMSO (up to 6 mg/ml).Physical Properties:Yellow lyophilized solidPurity:98% by HPLC
NMR (Conforms)Storage Temperature:-20°Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.Shipping Code:RT -
Borrelidin | Angiogenesis inhibitor
From $190.00CAS:7184-60-3Catalog Number:10-1399Activity:Angiogenesis inhibitorAlternate Names:U-78548; C2989; TreponemycinChemical Name:Fermentation from Streptomyces sp.Molecular Weight:489.66Molecular Formula:C28H43NO6Solubility:Soluble in DMSO or in Ethanol.Physical Properties:Off-white solidPurity:98% by HPLC
NMR (Conforms)Storage Temperature:-20°C (des.)Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.Shipping Code:RT
Calculate the molar concentration, mass or volume in a solution.
Concentration × Volume × Molecular Weight = Mass
