VS-4718 (PND-1186)

Catalog No.S7653 Batch:S765304

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Technical Data

Formula

C25H26F3N5O3
Molecular Weight 501.5 CAS No. 1061353-68-1
Solubility (25°C)* In vitro DMSO 100 mg/mL (199.4 mM)
Water Insoluble
Ethanol Insoluble
In vivo (Add solvents to the product individually and in order)
Homogeneous suspension
CMC-NA
≥5mg/ml Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

Biological Activity

Description VS-4718 (PND-1186) is a reversible and selective FAK inhibitor with IC50 of 1.5 nM, which selectively promotes tumor cell apoptosis. Phase 1.
Targets
FAK [1]
(Cell-free assay)
1.5 nM
In vitro In vitro, VS-4718 (PND-1186) inhibits 4T1 breast carcinoma motility, promotes 4T1 apoptosis in suspended conditions, and decreases 4T1 soft agar colony number and size. [1] This compound also promotes G0-G1 cell-cycle arrest followed by cell death in HEY and OVCAR8 cells. [2]
In vivo In mice bearing 4T1 tumors, VS-4718 (PND-1186) (100 mg/kg s.c.) inhibits subcutaneous tumor growth by induction of apoptosis. This compound (0.5 mg/mL for p.o.) also causes ovarian carcinoma tumor growth inhibition in mice bearing ID8 tumors. [1]

Protocol (from reference)

Kinase Assay:

[1]
  • In vitro kinase activity

    VS-4718 (PND-1186) is evaluated by measuring GST-FAK in vitro kinase activity and comparing it to His-tagged FAK 411–686 using the K-LISA screening kit and poly(Glu:Tyr) (4:1) copolymer as a substrate immobilized on microtiter plates. IC50 values for this compound are determined with various concentrations in a buffer containing 50 µM ATP and 10 mM MnCl2, 50 mM HEPES (pH 7.5), 25 mM NaCl, 0.01% BSA, and 0.1 mM Na orthovanadate for 5 min at room temperature. Serial diluted compounds are tested in triplicate. Substrate phosphorylation is measured using horseradish peroxidase-conjugated anti-pTyr antibodies with spetrophotometric color quantitation. IC50 values are determined using the Hill-Slope Model. Kinase selectivity profiling is performed by using the KinaseProfiler service.
Cell Assay:

[1]
  • Cell lines

    Murine ID8 ovarian carcinoma cells

  • Concentrations

    ~1 μM

  • Incubation Time

    6 days

  • Method

    For soft agar assays, 48-well plates are coated with a 1:4 mix of 2% agar (EM Science) in 0.2 mL growth media (bottom layer). 5×104 cells are plated per well (in triplicate) in a mixture of 0.3% agar in 0.2 mL growth media (top layer). After agar solidification, 0.2 mL growth media is added containing DMSO or VS-4718 (PND-1186) (final concentration for 0.6 mL). In separate experiments, this compound is added after 4 days. After 10 days, colonies are imaged in phase contrast, enumerated by counting 9 fields (3 fields per well), and total area determined using Image J. For all analyses, experimental points are performed in triplicate and repeated at least two times.
Animal Study:

[1]
  • Animal Models

    Mice bearing ID8 tumors or 4T1 tumors

  • Dosages

    100 mg/kg every 12 hours for s.c.; 0.5 mg/mL for p.o.

  • Administration

    s.c. or p.o.

References

  • https://pubmed.ncbi.nlm.nih.gov/20234191/
  • https://pubmed.ncbi.nlm.nih.gov/24899686/

Customer Product Validation

<p>(a) Percentage of apoptotic HepG2 and Huh7.5 cells after 48 h of treatment with DMSO (Vehicle), 0.5 μM or 1 μM PND 1186 measured by Annexin V and flow cytometry. Values are plotted as mean±SD (*P<0.05; **P<0.01; versus Vehicle, n =3). (b) Representative WB for p21 and caspase-3 in HepG2 and Huh7.5 cells after 48 h of treatment with DMSO (0), 0.5 μM or 1 μM PND 1186. β-tubulin is reported as a loading control (n=2). (c) Relative mRNA expression of EZH2 and NOTCH2 genes as measured by qRT-PCR in HepG2 and Huh7.5 cells after 48 h of treatment with DMSO (Vehicle), 0.5 μM or 1 μM PND 1186 (*P<0.05; **P<0.01; versus Vehicle, n =3).</p>

, , Cell Death Differ, 2017, 24(5):889-902

<p>Cells treated with different concentrations of VS-4718 for 24 h on 3D Matrigel culture were immunostained for cleaved caspase-3 and F-actin (d), and observed using confocal microscopy. Images are representative of cells treated with 10 μM VS-4718. Arrowheads (d) indicate cleaved caspase-3 activity. Data are presented as the means±s.d. of three independent experiments. The bar graphs show the average proportion of PI-positive spheroids. *P<0.01. Scale bar, 50 μm.</p>

, , Oncogene, 2017, 36(39):5522-5531

Cells were added equally to coverslips pretreated with fibronectin at 10 g/ml. Kinase inhibitors were then applied to these cells at the indicated concentrations. U0126 is a MAP kinase inhibitor, PND1186 is an FAK kinase inhibitor, saracatinib is an Src kinase inhibitor, and wortmannin is a PI3K inhibitor. Twenty-five minutes later, cells were pulsed with 2mM5-FUrd for 10 min. Cells werethen instantly fixed and stained with anti-BrdU antibody to visualize newly synthesized RNA in situ. Representative images are shown. (First column) 5-FUrd staining. Magnification, ×10. (Third column) 5-FUrd staining. Magnification, ×40. (Second and fourth columns) DAPI staining.

Data from [ , , Molecular and Cellular Biology, 2016, 36(10):1555-1568. ]

HIEC cells were treated with FAK inhibitor (1 μM VS-4718), or DMSO for 24 h, then exposed to 5 Gy of radiation and samples were taken 6 and 24 h later. Levels of FAK, p-FAK, and γH2AX were examined using western blotting and GAPDH was used as a loading control.

Data from [ , , Toxicol Appl Pharmacol, 2018, 360:131-140 ]

Selleck's VS-4718 (PND-1186) Has Been Cited by 49 Publications

Chromosomal 3p loss and 8q gain drive vasculogenic mimicry via HIF-2α and VE-cadherin activation in uveal melanoma [ Cell Death Differ, 2025, 10.1038/s41418-025-01469-9] PubMed: 40000790
Focal adhesion kinase plays an essential role in Th17 cell differentiation by stimulating NF-κB signaling [ Front Immunol, 2025, 16:1596802] PubMed: 41050684
Exosomal Galectin-3 promotes peritoneal metastases in gastric adenocarcinoma via microenvironment alterations [ iScience, 2025, 28(1):111564] PubMed: 39811647
The role of focal adhesion kinase in bladder cancer: translation from in vitro to ex vivo human urothelial carcinomas [ Radiol Oncol, 2025, 59(3):349-367] PubMed: 40959921
Focal adhesion kinase-YAP signaling axis drives drug-tolerant persister cells and residual disease in lung cancer [ Nat Commun, 2024, 15(1):3741] PubMed: 38702301
Focal adhesion kinase-YAP signaling axis drives drug-tolerant persister cells and residual disease in lung cancer [ Nat Commun, 2024, 15(1):3741] PubMed: 38702301
Viral infection induces inflammatory signals that coordinate YAP regulation of dysplastic cells in lung alveoli [ J Clin Invest, 2024, 134(19)e176828] PubMed: 39352385
Notochord segmentation in zebrafish controlled by iterative mechanical signaling [ Dev Cell, 2024, S1534-5807(24)00238-7] PubMed: 38697108
Pivotal role of IL-8 derived from the interaction between osteosarcoma and tumor-associated macrophages in osteosarcoma growth and metastasis via the FAK pathway [ Cell Death Dis, 2024, 15(2):108] PubMed: 38302407
Recycling machinery of integrin coupled with focal adhesion turnover via RAB11-UNC13D-FAK axis for migration of pancreatic cancer cells [ J Transl Med, 2024, 22(1):800] PubMed: 39210440

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