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Chemical Structure| 442632-72-6 Chemical Structure| 442632-72-6

Structure of CK-636
CAS No.: 442632-72-6

Chemical Structure| 442632-72-6

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CK-636 is an Arp2/3 complex inhibitor with IC50 of 4 μM, 24 μM and 32 μM for inhibition of actin polymerization induced by human, fission yeast and bovine Arp2/3 complex, respectively.

Synonyms: CK-0944636

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Product Details of CK-636

CAS No. :442632-72-6
Formula : C16H16N2OS
M.W : 284.38
SMILES Code : O=C(C1=CC=CS1)NCCC2=C(C)NC3=C2C=CC=C3
Synonyms :
CK-0944636
MDL No. :MFCD03036245
InChI Key :ACAKNPKRLPMONU-UHFFFAOYSA-N
Pubchem ID :588963

Safety of CK-636

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H317
Precautionary Statements:P280

Related Pathways of CK-636

cytoskeleton

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
SKOV3 cells 100 μM 60 minutes Inhibition of actin filament comet tail formation by Listeria monocytogenes PMC2780427
THP-1 monocytes 100 μM 15 minutes Inhibition of podosome formation by monocytes PMC2780427
Keratinocytes 40 μM Inhibited Arp2/3 complex activity, reducing Listeria-induced F-actin assembly PMC3791730
Pfa1 cells 100 μM 72 hours CK-636 significantly attenuated tamoxifen-induced ferroptosis PMC11625328
293T cells 100 μM 24 hours CK-636 significantly attenuated RSL3-induced ferroptosis PMC11625328
HT1080 cells 100 μM 24 hours CK-636 significantly attenuated RSL3-induced ferroptosis PMC11625328
T cells 50 μM Inhibition of Arp2/3, reducing lamellipodia formation at the leading edges of T cells, resulting in decreased migration speed on complex nanotopographical surfaces PMC3771970

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice Renal ischemia-reperfusion injury model Intraperitoneal injection 30 mg/kg 24 hours and 2 hours before surgery CK-666 significantly alleviated renal ischemia-reperfusion injury and ferroptosis PMC11625328

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.52mL

0.70mL

0.35mL

17.58mL

3.52mL

1.76mL

35.16mL

7.03mL

3.52mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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