MLN0905

CAS No. 1228960-69-7

MLN0905( MLN0905 | MLN 0905 | MLN-0905 )

Catalog No. M17207 CAS No. 1228960-69-7

MLN0905 is an effective PLK1 inhibitor(IC50=2 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 86 Get Quote
5MG 132 Get Quote
10MG 224 Get Quote
25MG 421 Get Quote
50MG 602 Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    MLN0905
  • Note
    Research use only, not for human use.
  • Brief Description
    MLN0905 is an effective PLK1 inhibitor(IC50=2 nM).
  • Description
    MLN0905 is a potent, selective small-molecule PLK1 inhibitor. MLN0905 inhibits cell proliferation in a broad range of human tumor cells including DLBCL cell lines. PLK1 inhibition leads to pharmacodynamic pHisH3 modulation and significant antitumor activity in multiple DLBCL models. These data strongly suggest evaluating PLK1 inhibitors as DLBCL anticancer agents in the clinic. (source: Mol Cancer Ther; 11(9); 2045-53.)
  • In Vitro
    ——
  • In Vivo
    Animal Model:Tumor (HT29) xenograft modelDosage:0-50 mg/kg Administration:P.O; daily, QD×3/week Result:Observed antitumor activity, tumor stasis or regression and well-tolerated oral doses.
  • Synonyms
    MLN0905 | MLN 0905 | MLN-0905
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Factor Xa
  • Recptor
    PLK1
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1228960-69-7
  • Formula Weight
    486.56
  • Molecular Formula
    C24H25F3N6S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 30 mg/mL. 61.66 mM
  • SMILES
    CN(C)CCCc1cc(Nc2ncc3CC(=S)Nc4c(ccc(c4)C(F)(F)F)c3n2)c(C)nc1
  • Chemical Name
    2-((5-(3-(dimethylamino)propyl)-2-methylpyridin-3-yl)amino)-9-(trifluoromethyl)-5H-benzo[b]pyrimido[4,5-d]azepine-6(7H)-thione

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Duffey MO, et al. J Med Chem, 2012, 55(1), 197-208.
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