CAS NO: | 1397922-61-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 |
Pyrotinib dimaleate (SHR-1258 dimaleate) is a potent and selectiveEGFR/HER2dual inhibitor withIC50s of 13 and 38 nM, respectively[1]. |
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IC50& Target[1] |
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体外研究 (In Vitro) |
Pyrotinib dimaleate has high potency in HER2-dependent cell lines (BT474, SK-OV-3), while showing much weaker inhibition in the HER2 negative cell line (MDA-MB-231). Pyrotinib dimaleate inhibits BT474 and SK-OV-3 cells with IC50s of 5.1 and 43 nM, respectively. Pyrotinib dimaleate displays high selectivity as HKI-272 when tested in a panel of different kinases such as KDR, c-Kit, PDGFRβ, c-Src and C-Met (c-Src with an IC50of 790 nM, and others >3000 nM)[1].
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体内研究 (In Vivo) |
Pyrotinib dimaleate has acceptable bioavailability of 20.6%, 43.5% and 13.5% in nude mice, rats and dogs, respectively. Pyrotinib dimaleate has favorable drug-like physicochemical properties and shows relatively higher oral exposure in human subjects (oral; t1/2=15 h) with a much longer half life than that of preclinical animal species such as mouse (i.v.; t1/2=1.56 h; i.g.; t1/2=2.52 h) and rat (i.v.; t1/2=4.42 h; i.g.; t1/2=3.38 h)[1].
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Clinical Trial |
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分子量 |
815.22 |
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性状 |
Solid |
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Formula |
C40H39ClN6O11 |
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CAS 号 |
1397922-61-0 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
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溶解性数据 |
In Vitro:
H2O : ≥ 106 mg/mL(130.03 mM) DMSO : 100 mg/mL(122.67 mM;Need ultrasonic) *"≥" means soluble, but saturation unknown.
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In Vivo:
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