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Home > Products >  WZ4003

WZ4003

  • Min.Order: 1 Gram
  • Payment Terms: L/C,T/T,
  • Product Details

Keywords

  • WZ4003

Quick Details

  • ProName: WZ4003
  • Appearance: white powder
  • Application: for laboratory research
  • DeliveryTime: within 3 days after payment
  • PackAge: Aluminium foil bag packing
  • Port: Shanghai, Shenzhen, Guangzhou, Hongkon...
  • ProductionCapacity: 1 Kilogram/Day
  • Purity: >99%
  • Storage: Kept in a cool, dry and ventilated pla...
  • Transportation: by air; by sea; by express
  • LimitNum: 1 Gram
  • Heavy metal: <0.002%
  • Grade: Industrial Grade

Superiority

 

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Details

 

Technical Data

Molecular Weight (MW) 496.99
Formula

C25H29ClN6O3

CAS No. 1214265-58-3
Synonyms N/A
Solubility (25°C)  
 
 
Storage 2 years -20℃Powder
6 months-80℃in DMSO
Chemical Name Propanamide, N-?[3-?[[5-?chloro-?2-?[[2-?methoxy-?4-?(4-?methyl-?1-?piperazinyl)?phenyl]?amino]?-?4-?pyrimidinyl]?oxy]?phenyl]?-
 

Preparing Stock Solutions

Biological Activity

Description WZ4003 is a highly specific NUAK kinase inhibitor with IC50 of 20 nM and 100 nM for NUAK1 and NUAK2, respectively, without significant inhibition on 139 other kinases.
Targets NUAK1 NUAK2        
IC50 20 nM  100 nM [1]        
In vitro In HEK-293 cells expressing wild-type NUAK1, WZ4003 (3–10 μM) markedly suppresses NUAK1-mediated MYPT1 phosphorylation. Moreover, WZ4003 (10 μM) inhibits MYPT1 Ser445 phosphorylation as well as cell migration, invasion and proliferation to a similar extent as knock out in MEFs or knock down in U2OS cells of NUAK1. [1] WZ4003 also exhibits a high, specific affinity to the L858R/T790M mutant EGFR, while a significantly reduced cellular IC50 against T790M containing Ba/F3 cells. [2]
In vivo  
Features  

 

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