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受注:045-509-1970 |
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Synonyms | N/A | Storage (From the date of receipt) |
3 years -20°C powder 1 years -80°C in solvent |
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| 化学式 | C25H30N6O3 |
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| 分子量 | 462.54 | CAS No. | 1009298-59-2 | ||||
| Solubility (25°C)* | 体外 | DMSO | 92 mg/mL (198.9 mM) | ||||
| Water | Insoluble | ||||||
| Ethanol | Insoluble | ||||||
| 体内 (毎回新しく調製した物を用意してください) |
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* <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. |
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| 製品説明 | Vistusertib (AZD2014) is a novel mTOR inhibitor with IC50 of 2.8 nM in a cell-free assay; highly selective against multiple PI3K isoforms (α/β/γ/δ). AZD2014 showed no or weak binding to the majority of kinases when tested at 1 μM. AZD2014 induces proliferation suppression, apoptosis, cell cycle arrest, and autophagy in HCC cells with antitumor activity. |
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| in vitro | Vistusertib (AZD2014) is a close analogue of AZD8055 and a selective inhibitor of mTOR kinase. It has greater inhibitory activity against mTORC1 compared to rapamycin: this compound decreases p4EBP1 Thr37/46, inhibits the translation initiation complex and decreases overall protein synthesis while rapamycin has no effect. It also inhibits the mTORC2 biomarkers pAKTSer473 and pNDRG1Thr346. AZD2014 has broad antiproliferative activity across multiple tumour cell lines. In particular, it induces growth inhibition and cell death in breast cancer cell lines, including ER+ cell lines with acquired resistance to hormone therapy. [1] |
| in vivo | Vistusertib (AZD2014) induces tumour growth inhibition against several xenograft models including a human primary explant model of ER+ breast cancer. This antitumour activity is associated with modulation of both mTORC1 and mTORC2 substrates. [1] |
| 細胞アッセイ | 細胞株 | Cell-free assays |
|---|---|---|
| 濃度 | 2.81 nM | |
| 反応時間 | ||
| 実験の流れ | ||
| 動物実験 | 動物モデル | Male SCID mice |
| 投薬量 | 20 mg/kg | |
| 投与方法 | p.o. |
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Data from [Biochem Biophys Res Commun, 2014, 443(2), 406-12]

Data from [Biochem Biophys Res Commun, 2014, 443(2), 406-12]

Data from [Biochem Biophys Res Commun, 2014, 443(2), 406-12]
| A phase II trial of mTORC1/2 inhibition in STK11 deficient non small cell lung cancer [ NPJ Precis Oncol, 2025, 9(1):67] | PubMed: 40069402 |
| Volatilomic response to targeted cancer therapy in vitro [ Sci Rep, 2025, 15(1):19445] | PubMed: 40461777 |
| Effects of simulated microgravity on colorectal cancer organoids growth and drug response [ Sci Rep, 2024, 14(1):25526] | PubMed: 39462078 |
| USP9X mediates an acute adaptive response to MAPK suppression in pancreatic cancer but creates multiple actionable therapeutic vulnerabilities [ Cell Rep Med, 2023, 4(4):101007] | PubMed: 37030295 |
| m7G-related genes predict prognosis and affect the immune microenvironment and drug sensitivity in osteosarcoma [ Front Pharmacol, 2023, 14:1158775] | PubMed: 37654606 |
| Co-Targeting FASN and mTOR Suppresses Uveal Melanoma Growth [ Cancers (Basel), 2023, 15(13)3451] | PubMed: 37444561 |
| Co-Targeting FASN and mTOR Suppresses Uveal Melanoma Growth [ Cancers (Basel), 2023, 15(13)3451] | PubMed: 37444561 |
| Drug-Dependent Morphological Transitions in Spherical and Worm-Like Polymeric Micelles Define Stability and Pharmacological Performance of Micellar Drugs [ Small, 2022, 18(4):e2103552] | PubMed: 34841670 |
| High-risk neuroblastoma with NF1 loss of function is targetable using SHP2 inhibition [ Cell Rep, 2022, 40(4):111095] | PubMed: 35905710 |
| Reciprocal effects of mTOR inhibitors on pro-survival proteins dictate therapeutic responses in tuberous sclerosis complex [ iScience, 2022, 25(11):105458] | PubMed: 36388985 |
長期の保管のために-20°Cの下で製品を保ってください。
人間や獣医の診断であるか治療的な使用のためにでない。
各々の製品のための特定の保管と取扱い情報は、製品データシートの上で示されます。大部分のSelleck製品は、推薦された状況の下で安定です。製品は、推薦された保管温度と異なる温度で、時々出荷されます。長期の保管のために必要とされてそれと異なる温度で、多くの製品は、短期もので安定です。品質を維持するが、夜通しの積荷のために最も経済的な貯蔵状況を用いてあなたの送料を保存する状況の下に、製品が出荷されることを、我々は確実とします。製品の受領と同時に、製品データシートの上で貯蔵推薦に従ってください。