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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 49 In Stock
5MG 88 In Stock
10MG 118 In Stock
25MG 228 In Stock
50MG 397 In Stock
100MG 584 In Stock
500MG 1251 In Stock
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Biological Information

  • Product Name
    MI-2
  • Note
    Research use only, not for human use.
  • Brief Description
    MI-2 (MALT1 inhibitor) is a selective, irreversible MALT1 paracaspase inhibitor with IC50 of 5.84 uM.
  • Description
    MI-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.
  • 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. 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.
  • 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. 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.
  • Synonyms
    MI 2 | MI2
  • Pathway
    NF-κB
  • Target
    MALT1
  • Recptor
    MALT1
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    1047953-91-2
  • Formula Weight
    455.7223
  • Molecular Formula
    C19H17Cl3N4O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 46 mg/mL
  • SMILES
    O=C(NC1=CC=C(N2N=C(OCCOC)N=C2C3=CC=C(Cl)C(Cl)=C3)C=C1)CCl
  • Chemical Name
    Acetamide, 2-chloro-N-[4-[5-(3,4-dichlorophenyl)-3-(2-methoxyethoxy)-1H-1,2,4-triazol-1-yl]phenyl]-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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.