Name | WZ811 |
Synonyms | WZ811 WZ 811 N,N'-Di-2-pyridinyl-1,4-benzenedimethanamine N1,N4-Di-2-pyridinyl-1,4-benzenedimethanamine 1,4-Benzenedimethanamine, N1,N4-di-2-pyridinyl- N,N'-(1,4-PHENYLENEBIS(METHYLENE))DIPYRIDIN-2-AMINE N,N'-(1,4-phenylenebis(methylene))bis(pyridin-2-amine) N1,N4-di-2-pyridinyl-1,4-benzenedimethanamine WZ811 WZ 811 N,N'-Di-2-pyridinyl-1,4-benzenedimethanamine |
CAS | 55778-02-4 |
EINECS | 200-256-5 |
Molecular Formula | C18H18N4 |
Molar Mass | 290.36 |
Density | 1.229±0.06 g/cm3(Predicted) |
Melting Point | 192-194℃ (methanol ) |
Boling Point | 493.2±35.0 °C(Predicted) |
Solubility | DMSO: 28 mg/mL (96.4 mM)Ethanol: <1 mg/mL( < 1 mg/ml refers to the product slightly soluble or insoluble) |
Appearance | powder |
Color | white to tan |
pKa | 6.55±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
Use | WZ811 is an orally active, highly competitive CXCR4 agonist. WZ811 effectively inhibited CXCR4/SDF-1 (also known as CXCL12) -mediated cAMP level regulation (EC50=1.2 nM) and SDF-1-induced stromal gel invasion (EC50=5.2 nM) in cells. |
Target | CXCR4 |
In vitro study | WZ811 is a highly potent, competitive CXCR4 antagonist. WZ811, at doses as low as a few nanomolar, was effective in counteracting the SDF-1 reduction in cAMP. WZ811 inhibited SDF-1 mediated invasion with an EC50 of 5.2 nM. |
Hazard Symbols | Xn - Harmful |
Risk Codes | R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.444 ml | 17.22 ml | 34.44 ml |
5 mM | 0.689 ml | 3.444 ml | 6.888 ml |
10 mM | 0.344 ml | 1.722 ml | 3.444 ml |
5 mM | 0.069 ml | 0.344 ml | 0.689 ml |
biological activity | WZ811 is an efficient, competitive CXCR4 antagonist with EC50 of 0.3 nM. |
in vitro studies | WZ811 is a highly effective, competitive CXCR4 antagonist. WZ811 effectively counteracts SDF-1 reduction in cAMP at doses as low as a few nanomoles. WZ811 inhibits SDF-1-mediated invasion with EC50 of 5.2 nM. |