2. Cell Cycle/DNA Damage TGF-beta/Smad Stem Cell/Wnt Cytoskeleton
  3. ROCK
  4. WF-536

WF-536 is an orally active inhibitor of Rho-associated coiled-coil-containing protein kinase (ROCK). WF-536 has tumor anti-metastatic activity. WF-536 can be used for the research of cancer.

For research use only. We do not sell to patients.

WF-536 Chemical Structure

WF-536 Chemical Structure

CAS No. : 539857-64-2

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WF-536 Related Antibodies

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Description

WF-536 is an orally active inhibitor of Rho-associated coiled-coil-containing protein kinase (ROCK). WF-536 has tumor anti-metastatic activity. WF-536 can be used for the research of cancer[1].

In Vitro

WF-536 (1, 3, 10, 30, 100 μM) inhibits both invasion and migration by LLC cells and invasion, migration, and formation of capillarylike tubes on Matrigel by endothelial cells, without cytotoxicity or anti-proliferative action in either cell type[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

WF-536 Related Antibodies

Cell Migration Assay [1]

Cell Line: LLC cells, Human umbilical vein endothelial cells
Concentration: 1, 3, 10, 30 μM
Incubation Time: 6 h (tumor cells), 4 h (endothelial cells)
Result: Significantly inhibited LLC-cell migration, with inhibitory rates of 23% and 44% at 10 and 30 μM, respectively.

Cell Invasion Assay[1]

Cell Line: LLC cells, Human umbilical vein endothelial cells
Concentration: 1, 3, 10, 30 μM
Incubation Time: 18 h
Result: Showed significant and concentration-dependent inhibition of LLC-cell invasion.

Cell Proliferation Assay[1]

Cell Line: LLC cells, Human umbilical vein endothelial cells
Concentration: 1, 30, 100 μM
Incubation Time: 24, 48, 72, and 96 h
Result: Showed no significant effect at 1-30 μM on the proliferation up to 96 h incubation, although the proliferation was decreased at 100 μM over 48 h.
In Vivo

WF-536 (oral; 0.3-3 mg/kg/day; for 28 days) inhibits Lewis lung carcinoma (LLC) metastasis and LLC-induced angiogenesis in mice[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6 mice (male, 6-week old)[1]
Dosage: 0.3, 1, 3 mg/kg
Administration: Oral; daily; for 28 days
Result: Significantly reduced the number of pulmonary metastatic colonies of LLC in a dose-dependent manner (0.3- 3 mg/kg).
Molecular Weight

277.75

Formula

C14H16ClN3O
CAS No.
SMILES

O=C(C1=CC=C(C=C1)[C@@H](C)N)NC2=CC=NC=C2.Cl
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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WF-536 Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

WF-536539857-64-2WF536WF 536ROCKRho-associated protein kinaseRho-associated kinaseRho-kinaseROKRho-associated coiled-coil-containing protein kinase (ROCK)tumor metastasisoralcancerInhibitorinhibitorinhibit

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