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- 保存条件:
4°C, sealed storage, away from moisture
- 英文名:
AMN107 monohydrochloride monohydrate
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
10 mM * 1 mL/25 mg/50 mg/100 mg/200 mg/500 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥495.0 |
|---|---|---|---|
| 规格: | 25 mg | 产品价格: | ¥450.0 |
| 规格: | 50 mg | 产品价格: | ¥720.0 |
| 规格: | 100 mg | 产品价格: | ¥1150.0 |
| 规格: | 200 mg | 产品价格: | ¥1956.0 |
| 规格: | 500 mg | 产品价格: | ¥3912.0 |
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Nilotinib monohydrochloride monohydrate
CAS No. : 923288-90-8
MCE 国际站:Nilotinib monohydrochloride monohydrate
产品活性:Nilotinib monohydrochloride monohydrate 是一种二代酪氨酸酶抑制剂,有效抑制 BCR-ABL 及其突变体。
研究领域:Protein Tyrosine Kinase/RTK | Autophagy
In Vitro: Nilotinib (AMN107) monohydrochloride monohydrate, selective Abl inhibitor, is designed to interact with the ATP-binding site of BCR-ABL with a higher affinity than imatinib while being significantly more potent compared with imatinib (IC50<30 nM), also maintains activity against most of the BCR-ABL point mutants that confer Imatinib resistance.
?Nilotinib monohydrochloride monohydrate demonstrates significant antitumor efficacy against GIST xenograft lines and imatinib-resistant GIST cell lines which parent cell lines GK1C and GK3C shows imatinib sensitivity with IC50 of 4.59±0.97 μM and 11.15±1.48 μM, respectively, imatinib-resistant cell lines GK1C-IR and GK3C-IR shows Imatinib resistance with IC50 values of 11.74±0.17 μM (P<0.001) and 41.37±1.07 μM (P<0.001), respectively.
In Vivo: Nilotinib monohydrochloride monohydrate (oral gavage, 40 mg/kg, daily, 4 weeks) shows equivalent or higher antitumor effects in BALB/cSLc-nu/nu mice with GIST xenograft.
?Nilotinib monohydrochloride monohydrate has a significant healing effect on the macroscopic and microscopic pathologic scores and ensures considerable mucosal healing in the indomethacin-induced enterocolitis rat model while decreases the PDGFR α and β levels and apoptotic scores in the colon.
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文献和实验strategy to identify the spectrum of resistance-conferring mutations, which has helped in designing the next-generation BCR/ABL inhibitors such as Nilotinib, Dasatinib, and Ponatinib. Here we provide a detailed methodology for the screen
Assessment of Drug Transporter Function Using Fluorescent Cell Imaging
., Ambudkar, S.V., Neubauer, A., and Bates, S.E. 2010. Comparison of ATP‐binding cassette transporter interactions with the tyrosine kinase inhibitors imatinib, nilotinib, and dasatinib. Drug Metab. Dispos. 38:1371‐1380.
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