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WZ811
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。
WZ811图片
CAS NO:55778-02-4
规格:≥98%
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议
1g电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)290.36
FormulaC18H18N4
CAS No.55778-02-4
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 30 mg/mL (103.3 mM)
Water:<1 mg/mL
Ethanol:<1 mg/mL
Other info

Chemical Name: N,N'-(1,4-phenylenebis(methylene))bis(pyridin-2-amine)

InChi Key: KBVFRXIGQQRMEF-UHFFFAOYSA-N

InChi Code: InChI=1S/C18H18N4/c1-3-11-19-17(5-1)21-13-15-7-9-16(10-8-15)14-22-18-6-2-4-12-20-18/h1-12H,13-14H2,(H,19,21)(H,20,22)

SMILES Code: C1(CNC2=NC=CC=C2)=CC=C(CNC3=NC=CC=C3)C=C1

Synonyms

WZ811; WZ-811; WZ 811

实验参考方法
In Vitro

In vitro activity: WZ811 is a highly potent competitive antagonist of CXCR4. WZ811 is effective in counteracting SDF-1 on cAMP reduction at doses as low as a few nanomoles. WZ811 blocks SDF-1-mediated invasion with EC50 of 5.2 NM.


Cell Assay: In the cAMP assay, WZ811 reduces the effect on cAMP caused by 150ng/ml SDF-1 significantly. It also blocks the SDF-1 induced Matrigel invasion with EC50 value of 5.2nM. Since CXCR4 is involved in the pathogeneses of a wide range of infectious, inflammatory and other diseases, WZ811 is developed for the treatment of various CXCR4-related diseases. It is reported to have weak anti-HIV activity in cell culture.

In VivoWZ811 (40 mg/kg, p.o.) blocks the lymphocytic leukemia cells growth on mouse xenograft models, and inhibits CXCR4/PI3K/AKT signaling pathway in mouse xenograft model of lymphocytic leukemia
Animal modelMice
Formulation & Dosage40 mg/kg, p.o.
References

J Med Chem. 2007 Nov 15;50(23):5655-64.