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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 | C19H22F3N5O2S |
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| 分子量 | 441.47 | CAS No. | 1217486-61-7 | ||||
| Solubility (25°C)* | 体外 | DMSO | 88 mg/mL (199.33 mM) | ||||
| Ethanol (warmed with 50ºC water bath) | 59 mg/mL (133.64 mM) | ||||||
| Water | 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 | アルペリシブ (Alpelisib (BYL719)) はPI3Kβ/γ/δ に対する影響が最小限の、強力かつ選択的な PI3Kα 阻害剤(無細胞アッセイで IC50 = 5 nM) です。 臨床フェーズ2。 |
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| in vitro | Alpelisib (BYL719) inhibits the proliferation of breast cancer cell lines harboring PIK3CA mutations, correlating with inhibition of various downstream signaling components of the PI3K/Akt pathway. [1] |
| in vivo | Alpelisib (BYL719) shows statistically significant dose-dependent anti-tumor efficacy in PIK3CA mutant xenograft models in rodents at doses exceeding 270 mg/d. It has a low clearance, a half-life of 8.5 h and its exposure increases dose proportionally between 30mg/d and 450mg/d, displaying a low inter-individual variability in Cmax and AUC in human. At 270mg/d, this compound shows first signs of clinical efficacy include 1 confirmed partial response in a patient with ER+ breast cancer, and significant PET responses (PMR) and/or tumor shrinkage are achieved in 8 out of 17 evaluated patients. [1] |
| 細胞アッセイ | 細胞株 | CW2 cells |
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| 濃度 | 500 nM | |
| 反応時間 | 72 h | |
| 実験の流れ | Cells were treated with increasing concentrations of alpelisib (BYL719) (0–1000 nM) for 72 h, and cell viability was quantified using the CyQuant assay. |
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| 動物実験 | 動物モデル | Female athymic nu/nu mice |
| 投薬量 | 40 mg/kg | |
| 投与方法 | o.g. |
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Data from [Data independently produced by Br J Haematol, 2014, 165(1), 89-101]

, , Mol Cancer Ther, 2017, 16(4):637-648

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| Targeting PI3K inhibitor resistance in breast cancer with metabolic drugs [ Signal Transduct Target Ther, 2025, 10(1):92] | PubMed: 40113784 |
| Tamoxifen induces PI3K activation in uterine cancer [ Nat Genet, 2025, 57(9):2192-2202] | PubMed: 40846762 |
| MicroRNA-mediated PTEN downregulation as a novel non-genetic mechanism of acquired resistance to PI3Kα inhibitors of head & neck squamous cell carcinoma [ Drug Resist Updat, 2025, 81:101251] | PubMed: 40382983 |
| MicroRNA-mediated PTEN downregulation as a novel non-genetic mechanism of acquired resistance to PI3Kα inhibitors of head & neck squamous cell carcinoma [ Drug Resist Updat, 2025, 81:101251] | PubMed: 40382983 |
| Circulating tumor cell plasticity determines breast cancer therapy resistance via neuregulin 1-HER3 signaling [ Nat Cancer, 2025, 6(1):67-85] | PubMed: 39753722 |
| Whole-exome tumor-agnostic ctDNA analysis enhances minimal residual disease detection and reveals relapse mechanisms in localized colon cancer [ Nat Cancer, 2025, 10.1038/s43018-025-00960-z] | PubMed: 40301653 |
| RANKL/PD-1 dual blockade demonstrates survival benefit for patients with advanced lung adenocarcinoma harboring KRAS mutations [ Cell Rep Med, 2025, 6(7):102235] | PubMed: 40669444 |
| Oncogenic PIK3CA corrupts growth factor signaling specificity [ Mol Syst Biol, 2025, 21(2):126-157] | PubMed: 39706867 |
| The SGK3/GSK3β/β-catenin signaling promotes breast cancer stemness and confers resistance to alpelisib therapy [ Int J Biol Sci, 2025, 21(6):2462-2475] | PubMed: 40303291 |
| Role of the PI3K/AKT signaling pathway in the cellular response to Tumor Treating Fields (TTFields) [ Cell Death Dis, 2025, 16(1):210] | PubMed: 40148314 |
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。