
MI-2
CAS No. 1047953-91-2
MI-2( MI 2 | MI2 )
Catalog No. M10236 CAS No. 1047953-91-2
MI-2 (MALT1 inhibitor) is a selective, irreversible MALT1 paracaspase inhibitor with IC50 of 5.84 uM.
Purity : >98% (HPLC)






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2MG | 49 | In Stock |
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5MG | 88 | In Stock |
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10MG | 118 | In Stock |
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25MG | 228 | In Stock |
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50MG | 397 | In Stock |
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100MG | 584 | In Stock |
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500MG | 1251 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameMI-2
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NoteResearch use only, not for human use.
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Brief DescriptionMI-2 (MALT1 inhibitor) is a selective, irreversible MALT1 paracaspase inhibitor with IC50 of 5.84 uM.
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DescriptionMI-2 (MALT1 inhibitor) is a selective, irreversible MALT1 paracaspase inhibitor with IC50 of 5.84 uM, displays little activity against the related caspase family members caspase-3, -8, and -9; inhibits cleavage of MALT1 substrates, which is accompanied by NF-κB reporter activity suppression, c-REL nuclear localization inhibition, and NF-κB target gene downregulation; specifically suppress ABC-DLBCL in vitro and in vivo, exhibits GI 50 of 0.2, 0.5, 0.4, and 0.4 uM for HBL-1, TMD8, OCI-Ly3, and OCI-Ly10 cells respectively, inhibits nuclear translocation of RelB and p50, and decreases Bcl-xL levels in CLL cells.
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In VitroMALT1 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. Cell Proliferation Assay Cell Line:HBL-1, TMD8, OCI-Ly3, OCI-Ly10 cells Concentration:1, 10, 100, 1000 nM Incubation Time:48 hours Result:The GI50 in HBL-1, TMD8, OCI-Ly3, and OCI-Ly10 cells was 0.2, 0.5, 0.4, and 0.4 μM, respectively.Western Blot Analysis Cell Line:HBL-1 cells Concentration:62, 125, 250, 500, 1000 nM Incubation Time:24 hours Result:Inhibits MALT1 cleavage of CYLD in HBL-1 cells.
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In VivoMALT1 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. Animal Model:Eight-week-old male SCID NOD (bearing HBL-1 and TMD8 cells) Dosage:25 mg/kg Administration:Intraperitoneal injection; daily for 14 days Result:Profoundly suppressed the growth of both the TMD8 and HBL-1 ABC-DLBCL xenografts versus vehicle.
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SynonymsMI 2 | MI2
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PathwayNF-κB
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TargetMALT1
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RecptorMALT1
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number1047953-91-2
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Formula Weight455.7223
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Molecular FormulaC19H17Cl3N4O3
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 46 mg/mL
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SMILESO=C(NC1=CC=C(N2N=C(OCCOC)N=C2C3=CC=C(Cl)C(Cl)=C3)C=C1)CCl
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Chemical NameAcetamide, 2-chloro-N-[4-[5-(3,4-dichlorophenyl)-3-(2-methoxyethoxy)-1H-1,2,4-triazol-1-yl]phenyl]-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Fontan L, et al. Cancer Cell. 2012 Dec 11;22(6):812-24.
2. Saba NS, et al. Cancer Res. 2017 Dec 15;77(24):7038-7048.
3. Liu W, et al. Oncotarget. 2016 May 24;7(21):30536-49.
4. Yeh CN, et al. Oncotarget. 2017 Dec 8;8(69):113444-113459.
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MI-2
MI-2 (MALT1 inhibitor) is a selective, irreversible MALT1 paracaspase inhibitor with IC50 of 5.84 uM.