- 抑制劑
- 化合物庫
- 抗體
- 生物試劑
- 新產(chǎn)品
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別名: AP26113 中文名稱:布格替尼,布加替尼
Brigatinib是一種有效的、選擇性的ALK抑制劑,IC50=0.6 nM;也是ROS1抑制劑,IC50=0.9 nM。它還能以相對較低的效力抑制IGF-1R、FLT3、FLT3(D835Y)和EGFR。
Brigatinib Chemical Structure
CAS: 1197953-54-0
相關(guān)產(chǎn)品 | TAE684 (NVP-TAE684) GSK1838705A Repotrectinib (TPX-0005) AZD3463 AP26113-analog (ALK-IN-1) Ensartinib dihydrochloride ASP3026 | 點擊展開 |
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相關(guān)化合物庫 | 酪氨酸激酶抑制劑分子庫 PI3K/Akt 抑制劑庫 血管生成相關(guān)化合物庫 HIF-1信號通路化合物庫 FDA抗癌藥物庫 | 點擊展開 |
細胞系 | 實驗類型 | 給藥濃度 | 孵育時間 | 活性描述 | 文獻信息 |
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KARPAS299 | Antitumor assay | 50 mg/kg | 13 days | Antitumor activity against human KARPAS299 cells expressing NMP-ALK fusion protein xenografted in SCID/beige mouse assessed as tumor regression at 50 mg/kg, po administered once daily for 13 days, NULL = NULL μM. | 27144831 |
KARPAS299 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human ALK-positive KARPAS299 cells assessed as reduction in cell viability measured after 72 hrs by CellTiter 96 aqueous one solution cell proliferation assay, GI50 = 0.01 μM. | 27144831 | |
KARPAS299 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human ALK-positive KARPAS299 cells assessed as reduction in cell viability measured after 72 hrs by CellTiter 96 aqueous one solution cell proliferation assay, IC50 = 0.029 μM. | 27144831 | |
Ba/F3 | Function assay | 72 hrs | Inhibition of human EGFR del19/T790M/C797S mutant expressed in mouse Ba/F3 cells assessed as cell growth inhibition after 72 hrs by CellTiter-Glo assay, GI50 = 0.0672 μM. | 29136465 | |
BAF3 | Antiproliferative assay | 72 hrs | Antiproliferative activity against mouse BAF3 cells harboring EGFR 19D/T790M/C797S mutant after 72 hrs by resazurin dye based assay, IC50 = 0.26 μM. | 30429956 | |
BAF3 | Antiproliferative assay | 72 hrs | Antiproliferative activity against mouse BAF3 cells harboring EGFR L858R/T790M/C797S mutant after 72 hrs by resazurin dye based assay, IC50 = 0.42 μM. | 30429956 | |
NCI-H1975 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human NCI-H1975 cells harboring EGFR L858R/T790M mutant after 72 hrs by resazurin dye based assay, IC50 = 1.09 μM. | 30429956 | |
U937 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human ALK-negative U937 cells assessed as reduction in cell viability measured after 72 hrs by CellTiter 96 aqueous one solution cell proliferation assay, IC50 = 3.194 μM. | 27144831 | |
點擊查看更多細胞系數(shù)據(jù) |
產(chǎn)品描述 | Brigatinib是一種有效的、選擇性的ALK抑制劑,IC50=0.6 nM;也是ROS1抑制劑,IC50=0.9 nM。它還能以相對較低的效力抑制IGF-1R、FLT3、FLT3(D835Y)和EGFR。 | |||||||||||
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靶點 |
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體外研究(In Vitro) | ||||
體外研究活性 | 除了ALK, IGF1R和InsR,brigatinib也能有效地抑制FLT3和ROS1,IC50分別為2.1 nM和1.9 nM。在1 μM時,brigatinib對c-Met或Ron沒有顯著活性[1]。Brigatinib可克服EGFR三突變體的耐藥性,這一活性依賴于ATP競爭性,對野生型EGFR的影響較小[2]。 | |||
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細胞實驗 | 細胞系 | U937細胞, Karpas-299細胞, H3122細胞 | ||
濃度 | -- | |||
孵育時間 | 72 h | |||
方法 | 將細胞用抑制劑處理72小時,檢測細胞生長情況,確定IC50值。 |
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實驗圖片 | 檢測方法 | 檢測指標 | 實驗圖片 | PMID |
Western blot |
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