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Formula | C28H35N7O2 |
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Molecular Weight | 501.62 | CAS No. | 398493-79-3 | |
Solubility (25°C)* | In vitro | DMSO | 100 mg/mL (199.35 mM) | |
Water | Insoluble | |||
Ethanol | 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.) |
Description | PHA-680632 is a potent inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 27 nM, 135 nM and 120 nM, respectively. It has 10- to 200-fold higher IC50 for FGFR1, FLT3, LCK, PLK1, STLK2, and VEGFR2/3. | |||||||||||
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Targets |
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In vitro | PHA-680632 potently inhibits all three Aurora kinases (A, B, and C) with IC50 values of 27, 135, and 120 nM, respectively. PHA-680632 is selective for Aurora kinases, with 10- to 200-fold higher IC50 for FGFR1, FLT3, LCK, PLK1, STLK2, VEGFR2, and VEGFR3, and with IC50 higher than 10 μM for another 22 kinases. PHA-680632 shows potent anti-proliferative effects in a wide range of cell types with IC50 values of 0.06–7.15 μM, including HeLa, HCT116, HT29, LOVO, DU145, and NHDF cells. PHA-680632 (0.5 μM) causes polyploidy in tumor cells. The mechanism of action of PHA-680632 is in agreement with inhibition of Aurora kinases. [1] PHA680632 in association with radiation leads to additive effects in cancer cells, especially in the p53-deficient cells. Combined ionising radiation (IR) and treatment of PHA680632 (100–400 nM) prior to IR leads to an enhancement of radiation-induced Annexin V positive cells, micronuclei formation, and Brca1 foci formation only in HCT116 cells with deficient p53, other than the p53 wild-type counterparts. [2] | |||||||||||
In vivo | HA-680632 (15–60 mg/kg) inhibits tumor growth in mice xenografts models of HL60, A2780, and HCT116 cells, by reducing tumor cell proliferation and increasing apoptosis. PHA-680632 (45 mg/kg) suppresses growth of activated ras-driven mammary tumors in mouse mammary tumor virus v-Ha-ras transgenic mice and results in complete tumor stabilization and partial regression. [1] |
Kinase Assay:[1] |
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Cell Assay:[1] |
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Animal Study:[2] |
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Data from [Data independently produced by Cancer Res, 2013, 73(10), 3168-80]
Data independently produced by , , Dr. Zhang of Tianjin Medical University
Primary cilia suppress the fibrotic activity of atrial fibroblasts from patients with atrial fibrillation in vitro [ Sci Rep, 2024, 14(1):12470] | PubMed: 38816374 |
Aurora kinase A regulates cancer-associated RNA aberrant splicing in breast cancer [ Heliyon, 2023, 9(7):e17386] | PubMed: 37415951 |
Aurora kinase A regulates cancer-associated RNA aberrant splicing in breast cancer [ Heliyon, 2023, 9(7):e17386] | PubMed: 37415951 |
Nuclear Aurora kinase A switches m6A reader YTHDC1 to enhance an oncogenic RNA splicing of tumor suppressor RBM4 [ Signal Transduct Target Ther, 2022, 7(1):97] | PubMed: 35361747 |
FOP Negatively Regulates Ciliogenesis and Promotes Cell Cycle Re-entry by Facilitating Primary Cilia Disassembly [ Front Cell Dev Biol, 2020, 8:590449] | PubMed: 33304902 |
Endothelial Cells Promote Colorectal Cancer Cell Survival by Activating the HER3-AKT Pathway in a Paracrine Fashion. [ Mol Cancer Res, 2019, 17(1):20-29] | PubMed: 30131447 |
Targeted Polo-like Kinase Inhibition Combined With Aurora Kinase Inhibition in Pediatric Acute Leukemia Cells. [ J Pediatr Hematol Oncol, 2019, 41(6):e359-e370] | PubMed: 30702467 |
HDAC2 promotes loss of primary cilia in pancreatic ductal adenocarcinoma. [ EMBO Rep, 2017, 18(2):334-343] | PubMed: 28028031 |
Lineage specificity of primary cilia in the mouse embryo. [Bangs FK, et al. Nat Cell Biol, 2015, 17(2):113-22] | |
Lineage specificity of primary cilia in the mouse embryo. [ Nat Cell Biol, 2015, 17(2):113-22] | PubMed: 25599390 |
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