KPT-185

Catalog No.S7125 Batch:S712501

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Technical Data

Formula

C16H16F3N3O3
Molecular Weight 355.31 CAS No. 1333151-73-7
Solubility (25°C)* In vitro DMSO 71 mg/mL (199.82 mM)
Ethanol 71 mg/mL (199.82 mM)
Water Insoluble
* <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.)

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Biological Activity

Description KPT-185 is a selective CRM1 inhibitor that induces growth inhibition and apoptosis in a panel of NHL cell lines with a median IC50 ~25 nM.
Targets
CRM1 [1]
In vitro KPT-185 significantly inhibits leukemia cell proliferation with IC50 ranging from 100 nM to 500 nM, and induces cell-cycle arrest and apoptosis of AML cell lines and primary AML blasts. KPT-185 reduces CRM1 protein protein level and shows a significant nuclear accumulation of CRM1 cargo proteins. [1] KPT-185 also inhibits proliferation and promotes apoptosis of pancreatic cancer cells without affecting human pancreatic ductal epithelial cells. [2]

Protocol (from reference)

Cell Assay:

[1]
  • Cell lines

    AML cell lines (MV4-11, Kasumi-1, OCI/AML3, MOLM-13, KG1a, and THP-1)

  • Concentrations

    ~10 μM

  • Incubation Time

    72 hours

  • Method

    Cells are seeded into 96-well plates and treated for 24, 48, and 72 hours with KPT-SINE at various concentrations ranging from 10 nM to 10 μM. Cell viability is evaluated using the cell proliferation reagent WST-1 according to the manufacturer's protocol. The absorbance of wells at 450 nm (reference wavelength, 650 nm) is measured with a microplate reader.

Customer Product Validation

Data from [Data independently produced by , , Biochem Biophys Res Commun, 2018, 503(3):1544-1549]

Selleck's KPT-185 has been cited by 8 publications

Discovery of compounds that reactivate p53 mutants in vitro and in vivo [ Cell Chem Biol, 2022, S2451-9456(22)00275-6] PubMed: 35948006
Targeted CRM1-inhibition perturbs leukemogenic NUP214 fusion proteins and exerts anti-cancer effects in leukemia cell lines with NUP214 rearrangements [ Oncotarget, 2020, 11(36):3371-3386] PubMed: 32934780
STK38 kinase acts as XPO1 gatekeeper regulating the nuclear export of autophagy proteins and other cargoes [ EMBO Rep, 2019, 20(11):e48150] PubMed: 31544310
NEDD4 protects vascular endothelial cells against Angiotensin II-induced cell death via enhancement of XPO1-mediated nuclear export. [ Exp Cell Res, 2019, 10.1016/j.yexcr.2019.111505] PubMed: 31326389
XPO1-mediated nuclear export of RNF146 protects from angiotensin II-induced endothelial cellular injury [Sheng Z Biochem Biophys Res Commun, 2018, 503(3):1544-1549] PubMed: 30029878
EGFR feedback-inhibition by Ran-binding protein 6 is disrupted in cancer. [ Nat Commun, 2017, 8(1):2035] PubMed: 29229958
Inhibiting PLK1 induces autophagy of acute myeloid leukemia cells via mammalian target of rapamycin pathway dephosphorylation. [Tao YF, et al. Oncol Rep, 2017, 37(3):1419-1429] PubMed: 28184925
Activation of Yap-Directed Transcription by Knockdown of Conserved Cellular Functions. [ J Biomol Screen, 2016, 21(3):269-76] PubMed: 26637552

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SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.

NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.