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E3330(APX-3330)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
E3330(APX-3330)图片
CAS NO:136164-66-4
规格:≥98%
包装与价格:
包装价格(元)
5mg询价
10mg询价
25mg询价
50mg询价
100mg询价
250mg询价
500mg询价

理化性质和储存条件
Molecular Weight (MW)378.46
FormulaC21H30O6
CAS No.136164-66-4
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 75 mg/mL (198.2 mM)
Water: 75 mg/mL (198.2 mM)
Ethanol: <1 mg/mL
Other info

Chemical Name: (E)-2-((4,5-dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)methylene)undecanoic acid

InChi Key: AALSSIXXBDPENJ-FYWRMAATSA-N

InChi Code: InChI=1S/C21H30O6/c1-5-6-7-8-9-10-11-12-15(21(24)25)13-16-14(2)17(22)19(26-3)20(27-4)18(16)23/h13H,5-12H2,1-4H3,(H,24,25)/b15-13+

SMILES Code: CCCCCCCCC/C(C(O)=O)=C\C1=C(C)C(C(OC)=C(OC)C1=O)=O

Synonyms

E3330; E-3330; E 3330.

实验参考方法
In Vitro

In vitro activity: E3330 affects hemangioblast development in vitro via inhibition of Ape1 redox activity. E3330 inhibits the growth of human pancreatic cancer cell line PANC1, XPA1, MIAPACA, BxPC3, and PK9. E3330 also promotes exit of cell cycle in PANC1 cells, inhibits the DNA-Binding activity of HIF-1α and migration of pancreatic cancer cells. In JHH6 cells, E3330 prevents the functional activation of NF-κB via the alteration of APE1 subcellular trafficking and reduces IL-6 and IL-8 expression induced by TNF-α and FAs accumulation through blockage of the redox-mediated activation of NF-κB.


Cell Assay: PANC1 cells are placed in one well of a 12-well plate and treated with 5 to 30 μM E3330. After a 24, 48, and 72 h of culture, the cells are washed with PBS and stained with trypan blue, and cell viability is examined by counting the live cell numbers.

In VivoIn mice with endotoxin-mediated hepatitis, E3330 (300 mg/kg, p.o.) attenuates the elevation of plasma tumor necrosis factor activity and protectes mice from liver injury. In Rat model, E3330 (100 mg/kg, p.o.) also protectes rats from severe liver injury induced with endotoxin plus galactosamine.
Animal modelMice with endotoxin-mediated hepatitis
Formulation & DosageSuspended in 0.5% methylcellulose solution; 300 mg/kg; p.o.
References

Blood. 2007 Mar 1;109(5):1917-22; J Pharmacol Exp Ther. 1992 Jul;262(1):145-50.

 
 
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