目錄:MedChemExpress LLC>>生化試劑>> MALT1 inhibitor MI-2 | MCE
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參考價(jià) | ¥ 1100 |
更新時(shí)間:2023-06-15 09:29:25瀏覽次數(shù):76評(píng)價(jià)
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CAS | 1047953-91-2 | 純度 | 99.88% |
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分子量 | 455.72 | 分子式 | C??H??Cl?N?O? |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 5 mg |
貨號(hào) | HY-12276 | 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. : 1047953-91-2
產(chǎn)品活性:MALT1 inhibitor MI-2 is a MALT1 inhibitor (IC50=5.84 μM). MALT1 inhibitor MI-2 binds directly to MALT1, irreversibly suppresses protease function and is accompanied by NF-κB reporter activity suppression, c-REL nuclear localization inhibition, and NF-κB target gene downregulation. MALT1 inhibitor MI-2 shows nontoxic to animals.
研究領(lǐng)域:Metabolic Enzyme/Protease | NF-κB
作用靶點(diǎn):MALT1
In Vitro: MALT1 inhibitor MI-2 (1-1000 nM; 48 hours) selectively suppresses MALT1-dependent DLBCL cell lines, and the GI50 in HBL-1, TMD8, OCI-Ly3, and OCI-Ly10 cells is 0.2, 0.5, 0.4, and 0.4 µM, respectively.
MALT1 inhibitor MI-2 (62-1000 nM; 24 hours) causes a dose-dependent decrease in MALT1-mediated cleavage.
In Vivo: MALT1 inhibitor MI-2 (25 mg/kg; i.p.; daily for 14 days) profoundly suppresses the growth of both the TMD8 and HBL-1 ABC-DLBCL xenografts.
相關(guān)產(chǎn)品:Covalent Screening Library Plus | Bioactive Compound Library Plus | Immunology/Inflammation Compound Library | Metabolism/Protease Compound Library | NF-κB Signaling Compound Library | Anti-Cancer Compound Library | Anti-Aging Compound Library | Covalent Screening Library | Targeted Diversity Library | MALT1-IN-3 | MLT-943 | MLT-231 | Mepazine hydrochloride | MALT1-IN-5 | MALT1-IN-6 | MALT1-IN-7 | MLT-747 | RGT-068A | MLT-748 | MALT1-IN-9 | NVS-MALT1 | (R)-MLT-985 | Z-VRPR-FMK TFA | Val-Arg-Pro-DL-Arg-Fluoromethylketone | MALT1-IN-8 | MALT1-IN-11 | Safimaltib
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