MDL | MFCD03036245 |
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Molecular Weight | 284.38 |
Molecular Formula | C16H16N2OS |
SMILES | O=C(C1=CC=CS1)NCCC2=C(C)NC3=C2C=CC=C3 |
CK-636 is a cell permeable inhibitor of Arp2/3 complex , that could inhibit actin polymerization, with IC 50 values of 4 μM, 24 μM and 32 μM for human, fission yeast and bovine, respectively. CK636 blocks cell migration.
IC50: 4/24/32 µM (Human/fission yeast/bovine Arp2/3) [1] .
CK-636 binds between Arp2 and Arp3, where it appears to block movement of Arp2 and Arp3 into their active conformation. CK-636 inserts into the hydrophobic core of Arp3 and alters its conformation. CK-636 prevents actin polymerization and the formation of actin filament comet tails by Listeria in infected SKOV3 cells (IC 50 =22 µM) [1] . Additionally, CK-636-treated T cells exhibits elongated morphology with sharp pseudopodia at the leading edges, while the breadth of the CK-636-treated T cells is about 30% less than that of DMSO-treated T cells [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
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4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : ≥ 49 mg/mL ( 172.30 mM )
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
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1 mM | 3.5164 mL | 17.5821 mL | 35.1642 mL |
5 mM | 0.7033 mL | 3.5164 mL | 7.0328 mL |
10 mM | 0.3516 mL | 1.7582 mL | 3.5164 mL |