Epertinib hydrochloride
CAS No. 2071195-74-7
Epertinib hydrochloride ( S-22611 hydrochloride )
产品货号. M23929 CAS No. 2071195-74-7
盐酸依帕替尼显示出有效的抗肿瘤活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1729 | 有现货 |
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| 10MG | ¥2736 | 有现货 |
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| 25MG | ¥4111 | 有现货 |
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| 50MG | ¥5794 | 有现货 |
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| 100MG | ¥7542 | 有现货 |
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| 200MG | ¥10170 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥2271 | 有现货 |
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生物学信息
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产品名称Epertinib hydrochloride
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述盐酸依帕替尼显示出有效的抗肿瘤活性。
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产品描述Epertinib hydrochloride shows potent antitumor activity.?Epertinib hydrochloride is a potent, orally active, reversible, and selective tyrosine kinase inhibitor of EGFR, HER2 and HER4, with IC50s of 1.48 nM, 7.15 nM and 2.49 nM, respectively.
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体外实验Epertinib hydrochloride inhibits the phosphorylation of EGFR and HER2 in NCI-N87 cells, with IC50 values of 4.5 and 1.6 nM, respectively.Epertinib hydrochloride shows inhibitory activity against MDA-MB-361 cell, with an IC50 of 26.5 nM.Epertinib hydrochloride (0-10 μM, 72 h) can selectively inhibit the proliferation of a range of cancer cell lines expressing EGFR and/or HER2. Cell Proliferation Assay Cell Line:NCI-N87 (stomach), BT-474 (breast), SK-BR-3 (breast), MDA-MB-453 (breast), MDA-MB-175VII (breast), HT115 (colon), Calu-3 (lung), fR2 (breast), and MRC-5 (lung) Concentration:0-10 μM Incubation Time:72 h Result:Inhibited the growth of NCI-N87, BT-474, SK-BR-3, MDA-MB-453, MDA-MB-175VII, HT115, Calu-3, fR2, and MRC-5, with IC50 values of 8.3 ± 2.6, 9.9 ± 0.8, 14.0 ± 3.6, 48.6 ± 3.1, 21.6 ± 4.3, 53.3 ± 8.6, 241.5 ± 29.2, 5366.7 ± 65.2, and 4964.6 ± 340.3.
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体内实验Epertinib hydrochloride (0-100 mg/kg, Orally, once daily for 28 days) shows antitumor activity.Epertinib hydrochloride (50 mg/kg, Orally, once daily for 30 days) significantly reduces the brain tumor volume.Epertinib hydrochloride (0-50 mg/kg, Orally, once daily for 10-28 days) significantly inhibits the tumor growth in a dose-dependent manner. Animal Model:Nude mice (BALB/cAJcl-nu/nu, implanted intracranially with MDA-MB-361 or BR2 cells)Dosage:12.5, 25, 50, 100 ?mg/kg Administration:Orally, once daily for 28 daysResult:Showed antitumor activity in the mammary fat pad implantation model using both cell lines and the ED50 values were comparable (24.1?mg/kg and 26.5?mg/kg for MDA-MB-361 and BR2 (MDA-MB-361-luc-BR2), respectively).Animal Model:Nude mice (BALB/cAJcl-nu/nu, implanted intracranially with MDA-MB-361 or BR2 cells)Dosage:50 mg/kg Administration:Orally, once daily for 30 days Result:Significantly reduced the brain tumor volume, indicating that epertinib could have potent antitumor activity in brain metastasis even in the presence of an intact BTB (blood-tumor barrier).Animal Model:Nude mice (BALB/cAJcl-nu/nu, prepared by subcutaneous implantation of human gastric cancer cells, NCI-N87 into the back of nude mice)Dosage:0, 6.25, 12.5, 25, and 50 mg/kg Administration:Oral gavage, daily for 10-28 days Result:Significantly inhibited the tumor growth in a dose-dependent manner.
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同义词S-22611 hydrochloride
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通路Angiogenesis
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靶点EGFR
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受体EGFR|HER4|HER2
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研究领域——
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适应症——
化学信息
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CAS Number2071195-74-7
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分子量596.48
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分子式C30H28Cl2FN5O3
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纯度>98% (HPLC)
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溶解度DMSO:125 mg/mL (209.56 mM; Need ultrasonic)
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SMILESCC#C/C(=N\OC[C@H]1COCCN1)/C2=CC3=C(C=C2)N=CN=C3NC4=CC(=C(C=C4)OCC5=CC(=CC=C5)F)Cl.Cl
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Tanaka H, et al. Preclinical antitumor activity of S-222611, an oral reversible tyrosine kinase inhibitor of epidermal growth factor receptor and human epidermal growth factor receptor 2. Cancer Sci. 2014 Aug;105(8):1040-8.
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