目錄:MedChemExpress LLC>>生化試劑>> MS170 | MCE
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更新時(shí)間:2023-06-13 10:06:14瀏覽次數(shù):131評(píng)價(jià)
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CAS | 2376136-61-5 | 分子量 | 870.44 |
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分子式 | C??H??ClN?O? | 供貨周期 | 現(xiàn)貨 |
規(guī)格 | 10 mg | 貨號(hào) | HY-145282 |
應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 2376136-61-5
產(chǎn)品活性:MS170 is a potent and selective PROTAC AKT degrader. MS170 depletes cellular total AKT (T-AKT) with the DC50 value of 32 nM. MS170 binds to AKT1, AKT2, and AKT3 with Kds of 1.3 nM, 77 nM, and 6.5 nM, respectively.
研究領(lǐng)域:PROTAC | PI3K/Akt/mTOR
作用靶點(diǎn):PROTACs | Akt
In Vitro: Cereblon (CRBN)-recruiting degrader MS170 is an effective AKT degrader without a ″hook effect″. MS170 selectively induces robust AKT protein degradation, inhibits downstream signaling, and suppresses cancer cell proliferation. MS170 concentration- and time-dependently induces AKT degradation through the ubiquitin-proteasome system (UPS).
MS170 (10 nM-10 μM) effectively inhibits the proliferation in multiple cancer cell lines.
MS170 (1 nM-10 μM) concentration-dependently depletes cellular total AKT (T-AKT) with the DC50 value of 32±18 nM.
In Vivo: MS170 (a single intraperitoneal injection at a dose of 50 mg/kg) is bioavailable in mice via IP injection.
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