Basic information Safety Supplier Related

CK-0157869

Basic information Safety Supplier Related

CK-0157869 Basic information

Product Name:
CK-0157869
Synonyms:
  • 2-(3-Bromophenyl)-3-(2,4-dimethoxyphenyl)-4-thiazolidinone
  • CK 869
  • CK-0157869
  • CK-869
  • CS-2870
  • CK-869; CK 869; CK869; CK-0157869; CK 0157869; CK0157869
  • 4-Thiazolidinone, 2-(3-bromophenyl)-3-(2,4-dimethoxyphenyl)-
  • CK869,Arp2/3 Complex,inhibit,CK-869,Inhibitor,CK 869,Actin-related protein 2/3 complex
CAS:
388592-44-7
MF:
C17H16BrNO3S
MW:
394.28
Mol File:
388592-44-7.mol
More
Less

CK-0157869 Chemical Properties

storage temp. 
2-8°C
solubility 
DMSO: soluble10mg/mL, clear
form 
powder
color 
white to light gray
More
Less

Safety Information

Hazard Codes 
N
Risk Statements 
50
Safety Statements 
61
WGK Germany 
3
More
Less

CK-0157869 Usage And Synthesis

Description

CK 869 is an inhibitor of actin polymerization via inhibition of the actin-related protein 2/3 (Arp2/3) complex, leading to reduced cell motility rate and rearrangement of F-actin in M-1 cells. It inhibits comet tail formation by L. monocytogenes with an IC50 value of 7 μM. It also impairs cell adhesion and cell spreading in MCF10A human breast epithelial cells.

Uses

CK-869 has been used as an Arp2/3 complex inhibitor:

  • to treat cultured mammalian cells and study its in vitro and in vivo effects on microtubule assembly
  • to induce membrane blebbing in HT1080 fibrosarcoma cells
  • to treat KDM3A-null cells and study the relation between actin dynamics and ciliogenesis

Uses

CK-869 binds to the Arp2/3 complex and inhibits nucleation. The Arp2/3 complex is involved with cell motility and F-actin reorganization in M-1 cells.

Biochem/physiol Actions

CK-0157869 (CK-869) prevents microtubule (MT) assembly, free of Arp2/3 complex.

References

[1] DARIA V ILATOVSKAYA. Arp2/3 complex inhibitors adversely affect actin cytoskeleton remodeling in the cultured murine kidney collecting duct M-1 cells.[J]. Cell and Tissue Research, 2013, 354 3: 783-792. DOI: 10.1007/s00441-013-1710-y
[2] B. J. NOLEN. Characterization of two classes of small molecule inhibitors of Arp2/3 complex[J]. Nature, 2009, 460 7258: 1031-1034. DOI: 10.1038/nature08231
[3] YVONNE BECKHAM. Arp2/3 inhibition induces amoeboid-like protrusions in MCF10A epithelial cells by reduced cytoskeletal-membrane coupling and focal adhesion assembly.[J]. PLoS ONE, 2014: e100943. DOI: 10.1371/journal.pone.0100943

CK-0157869Supplier

Nanjing Dulai Biotechnology Co., Ltd.
Tel
025-846993838003-8003 18013301590
Email
njduly@126.com
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Shanghai Lollane Biological Technology Co.,Ltd.
Tel
021-52996696,15000506266 15000506266
Shanghaizehan biopharma technology co., Ltd.
Tel
021-61350663 13052117465
Email
sales@zehanbiopharma.com
EMMX Biotechnology LLC
Tel
888-539-0666
Email
info@emmx.com
More
Less

CK-0157869(388592-44-7)Related Product Information