Irinotecan hydrochloride

製品コードS5026 バッチS502604

印刷

化学情報

 Chemical Structure Synonyms CPT-11 hydrochloride, (+)-Irinotecan hydrochloride Storage
(From the date of receipt)
3 years -20°C powder
化学式

C33H39ClN4O6

分子量 623.14 CAS No. 100286-90-6
Solubility (25°C)* 体外 DMSO 100 mg/mL (160.47 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)
Clear solution
2% DMSO 40% PEG 300 5%Tween80 53%ddH2O
2.0mg/ml Taking the 1 mL working solution as an example, add 20 μL of 100 mg/ml clarified DMSO stock solution to 400 μL of PEG300, mix evenly to clarify it; add 50 μL of Tween80 to the above system, mix evenly to clarify; then continue to add 530 μL of ddH2O to adjust the volume to 1 mL. The mixed solution should be used immediately for optimal results. 
Clear solution
2%DMSO 98%Corn oil
0.24mg/ml Taking the 1 mL working solution as an example, add 20 μL of 12 mg/ml clear DMSO stock solution to 980 μL of corn oil and mix evenly. The mixed solution should be used immediately for optimal results. 
* <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.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Irinotecan (CPT-11, (+)-Irinotecan) hydrochloride is an inhibitor of Topoisomerase I (Topo I) that exhibits cytotoxicity in LoVo cells and HT-29 cells with IC50 of 15.8 μM and 5.17 μM, respectively.
in vitro

The combination of gefitinib and irinotecan has a significant synergistic effect on the proliferation and migration of MDA-MB-231 cells.[2]

in vivo

The combination of gefitinib and irinotecan has a significant synergistic effect in the treatment of TNBC subtype cells in xenograft model.[2]

プロトコル(参考用のみ)

細胞アッセイ 細胞株 Human BC cell lines
濃度 32 μM
反応時間 24 h, 72 h
実験の流れ

Cells are seeded in 96-well plates at 6 × 103 cells/well for overnight incubation. The cells are exposed to irinotecan alone or combinations. Seventy-two hours after drug treatment, cell viability is tested with the MTT assay. For wound fealing assay, cells are seeded in 6-well culture plates at a density of 3 × 105 cells/mL. After growing to confluence, cells are treated with irinotecan for 48 h in DMEM.

動物実験 動物モデル Female BALB/c nude mice bearing MDA-MB-231 cells
投薬量 8 mg/kg
投与方法 i.p.

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Integrated genome and tissue engineering enables screening of cancer vulnerabilities in physiologically relevant perfusable ex vivo cultures [ Biomaterials, 2021, 280:121276] PubMed: 34890975

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。

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