化合物 FB23-2|T7138|TargetMol

價(jià)格	￥396	￥559	￥898
包裝	1mg	2mg	5mg

最小起訂量	1mg
發(fā)貨地	上海
更新日期	2025-02-28

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產(chǎn)品詳情

中文名稱:化合物 FB23-2	英文名稱:FB23-2
CAS:2243736-45-8	品牌: TargetMol
產(chǎn)地: 美國(guó)	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: 98.00%	產(chǎn)品類別: 抑制劑
貨號(hào): T7138

Product Introduction

Bioactivity

名稱	FB23-2
描述	FB23-2 is a potent and selective mRNA N6-methyladenosine (m6A) demethylase FTO inhibitor(IC50 : 2.6 μM).
細(xì)胞實(shí)驗(yàn)	Quantitation of FB23 and FB23-2 in AML cells: NB4 and MONOMAC6 cells were treated with 10 μM FB23 or FB23-2 for 24 hr, respectively. Viable cells were distinguished with 0.1% trypan blue, counted and then harvested with PBS by several washings. Cells were diluted into 100 μl with 50% (v/v) water/methanol and followed by several shock freeze-thaw cycles. The supernatants were collected for analysis. The Ultimate 3000 system coupled with a TSQ Quantiva mass spectrometer was applied to determine the cellular concentration of compound FB23 and FB23-2. Analytes were separated on a XSELECT? HSS T3 column (100 mm × 3.0 mm, 2.5 μm). The mobile phases used for elution were (A) 0.1% (v/v) formic acid/water and (B) 0.1% (v/v) formic acid/acetonitrile. The mass spectrometer was operated in the negative MRM mode. Parent-to-product transitions were m/z 375.1→339.1, 375.1→298.1 for FB23, and m/z 390.3→318.0, 390.3→289.9 for FB23-2, respectively[1].
動(dòng)物實(shí)驗(yàn)	The NSGS mice were bred and subjected to the xeno-transplantation model. For the AML mouse model, 0.2 × 10^6 MONOMAC6 cells were directly transplanted into NSGS mice via tail vein. After 10 days, FB23-2 (2 mg/kg/day) and DMSO vehicle were intraperitoneally injected into the mice for a continuous 10 days. The mice were euthanized by CO2 inhalation if they exhibited classical AML symptoms including hunched posture, paralysis, and reduced body weight. Meanwhile, the PB, spleen, and liver samples were collected for further analysis[1].
體外活性	FB23-2直接與FTO結(jié)合，選擇性抑制FTO的m6A去甲基化酶活性。模擬FTO耗盡，F(xiàn)B23-2顯著抑制人急性髓性白血病(AML)細(xì)胞系和原代AML細(xì)胞的增殖，并促進(jìn)其分化/凋亡 in vitro[1]。
體內(nèi)活性	FB23-2在異種移植小鼠中顯著抑制人類AML細(xì)胞系和原代細(xì)胞的進(jìn)展[1]。
存儲(chǔ)條件	Powder: -20°C for 3 years \| In solvent: -80°C for 1 year \| Shipping with blue ice.
溶解度	DMSO : 1 mg/mL (2.55 mM), Sonication is recommended.
關(guān)鍵字	myeloid \| mRNA N6-methyladenosine (m6A) demethylase FTO \| mRNA \| m6A \| leukemia \| Inhibitor \| inhibit \| FB23-2 \| FB-23-2 \| FB232 \| FB23 2 \| demethylase \| Apoptosis \| anti-proliferation \| AML \| acute
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相關(guān)庫(kù)	抑制劑庫(kù) \| 經(jīng)典已知活性庫(kù) \| 已知活性化合物庫(kù) \| 細(xì)胞凋亡化合物庫(kù) \| NO PAINS 化合物庫(kù) \| 表觀遺傳庫(kù) \| 抗肥胖化合物庫(kù) \| 血液病分子庫(kù)

關(guān)鍵字： FB23-2|TargetMol

公司簡(jiǎn)介

TargetMol Chemicals Inc. 總部位于馬薩諸塞州波士頓，致力于為全球生化領(lǐng)域科學(xué)家的研究提供專業(yè)的產(chǎn)品和服務(wù)。TargetMol?品牌的客戶群分布于40多個(gè)國(guó)家和地區(qū)，已發(fā)展成為全球知名的化合物庫(kù)和小分子化合物研究供應(yīng)商。 TargetMol?可提供160多種滿足不同需求的化合物庫(kù)，以及多種類型的生化試劑產(chǎn)品，包括12000多種抑制劑、16000多種天然產(chǎn)物和各類多肽、抗體、生命科學(xué)試劑盒等，此外，我們還建設(shè)有CADD（計(jì)算機(jī)輔助藥物設(shè)計(jì)）研究中心、藥理實(shí)驗(yàn)室、藥化合成平臺(tái)三大技術(shù)中心，全方位滿足客戶的定制需求。憑借我們優(yōu)質(zhì)的產(chǎn)品和服務(wù)、快速高效的全球供應(yīng)鏈和專業(yè)的技術(shù)支持，我們將有效幫助您縮短研發(fā)周期，取得更成功的結(jié)果。

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