價格 | ¥955 | ¥1570 | ¥2880 |
包裝 | 2mg | 5mg | 10mg |
最小起訂量 | 1mg |
發(fā)貨地 | 上海 |
更新日期 | 2024-12-12 |
中文名稱:化合物 Derazantinib | 英文名稱:Derazantinib |
CAS:1234356-69-4 | 品牌: TargetMol |
產(chǎn)地: 美國 | 保存條件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
純度規(guī)格: 99.95% | 產(chǎn)品類別: 抑制劑 |
貨號: TQ0228 |
名稱 | Derazantinib |
描述 | Derazantinib (ARQ-087) is a potent, ATP-competitive, orally active tyrosine kinase inhibitor with IC50 values ??of 4.5/1.8/4.35/3.4 nM for chondrocyte FGFR1/FGFR2/FGFR3/FGFR4, respectively. |
細(xì)胞實(shí)驗(yàn) | Cells are seeded at 3000-5000 cells per well with 130 μL media in 96-well tissue culture-treated plates. The cells are incubated overnight and subsequently treated with 3-fold serial dilutions of Derazantinib starting at 100 μM. The cells are returned to a 37°C humidified incubator for 72 hours. Cell proliferation is measured using the MTS assay [1]. |
激酶實(shí)驗(yàn) | Derazantinib is titrated in DMSO utilizing a 3-fold dilution scheme and then diluted 10-fold further in deionized water for a final DMSO concentration of 10%. A volume (2.5 μL) of these dilutions or vehicle is added to each well of a reaction plate. FGFR1 or FGFR2 is added to assay buffer to each well in a volume of 17.5 μL for a final concentration of 0.50 or 0.25 nM, respectively. After a 30-minute pre-incubation period, ATP and substrate are added in assay buffer (5 μL) for final concentrations of 0-1,000 μM ATP and 80 nM biotinylated-PYK2, for a final reaction volume of 25 μL. The plates are incubated for 60 minutes at room temperature and then stopped in the dark by the addition of 10 μL stop/detection mixture prepared in assay buffer containing EDTA [1]. |
動物實(shí)驗(yàn) | Female NCr nu/nu mice (SNU-16) or CB17 SCID mice (NCI-H716) with well established (400 mg) subcutaneous tumors are given a single oral dose of Derazantinib or vehicle control. Plasma and tumor samples are collected 4 hours post single dose. Derazantinib is administered orally. The dosing volume for all groups is 10 mL/kg or 0.1 mL/10 g body weight [1]. |
體外活性 | 方法:Derazantinib (ARQ-087)(0.1,0.3,1.1,3.3,10μM,2小時)處理異位表達(dá) FGFR1、FGFR2、FGFR3 或 FGFR4 的 COS-1 細(xì)胞,用 100 pM FGF1/2/7 刺激 15 分鐘,通過Western blot分析評估總FGFR和磷酸化FGFR。 結(jié)果:Derazantinib與EC一起抑制FGFR1、FGFR2、FGFR3和FGFR4的磷酸化IC50值分別為<0.123μM,0.185μM,0.463μM和>10μM。[1] |
體內(nèi)活性 | 方法:Derazantinib (ARQ-087)(25,50,75 mg/kg)處理 SNU-16和NCI-H716異種移植無胸腺小鼠模型;Derazantinib (50,100,150mg/kg)處理Ba/F3-FGFR2異種移植無胸腺小鼠模型;Derazantinib (75mg/kg)處理Ba/F3-INSR異種移植無胸腺小鼠模型;均采用口服的方式并評估評估 Derazantinib 的體內(nèi)抗腫瘤作用。 結(jié)果:Derazantinib在 Ba/F3-FGFR2 模型中顯示出有效的腫瘤生長抑制作用,而未能抑制 Ba/F3-INSR 模型的生長;在SNU-16異種移植研究中,用75 mg/kg和50 mg/kg處理分別達(dá)到83%和69%的TGI;在NCI-H716人盲腸模型中, 50 mg/kg 和 75 mg/kg 分別顯示出顯著的 TGI,分別為 68%和 96%。 [1] |
存儲條件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
溶解度 | DMSO : 98 mg/mL (209.15 mM) |
關(guān)鍵字 | ARQ087 | Fibroblast growth factor receptor | inhibit | FGFR | ARQ 087 | Inhibitor | Derazantinib |
相關(guān)產(chǎn)品 | Ponatinib | AZD4547 | Amlexanox | Lenvatinib | Formononetin | Lenvatinib mesylate | Ferulic Acid | Pazopanib | Nintedanib | Pemigatinib | Erdafitinib | Nintedanib esylate |
相關(guān)庫 | 抑制劑庫 | 經(jīng)典已知活性庫 | 抗癌活性化合物庫 | 已知活性化合物庫 | 激酶抑制劑庫 | 膜蛋白靶向化合物庫 | 酪氨酸激酶分子庫 | 藥物功能重定位化合物庫 | 抗癌臨床化合物庫 | 抗癌藥物庫 |
成立日期 | 2013-04-18 (12年) | 注冊資本 | 566.265100萬人民幣 |
員工人數(shù) | 100-500人 | 年?duì)I業(yè)額 | ¥ 1億以上 |
主營行業(yè) | 天然產(chǎn)物,生化試劑,分子生物學(xué),分子砌塊,生物技術(shù)服務(wù) | 經(jīng)營模式 | 貿(mào)易,工廠,試劑,定制,服務(wù) |
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