ZINC69391

CAS No. 303094-67-9

ZINC69391( ZINC-69391 | N'-(4,6-dimethylpyrimidin-2-yl)-N-[2-(trifluoromethyl)phenyl]guanidine )

Catalog No. M27796 CAS No. 303094-67-9

ZINC69391 is a selective inhibitor of Rac1 with antiproliferative and antimetastatic effects. ZINC69391 interferes with the interaction of Rac1 with Dock180, reduces Rac1-GTP levels and induces apoptosis.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 192 Get Quote
10MG 312 Get Quote
25MG 530 Get Quote
50MG 758 Get Quote
100MG 1044 Get Quote
500MG 2097 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    ZINC69391
  • Note
    Research use only, not for human use.
  • Brief Description
    ZINC69391 is a selective inhibitor of Rac1 with antiproliferative and antimetastatic effects. ZINC69391 interferes with the interaction of Rac1 with Dock180, reduces Rac1-GTP levels and induces apoptosis.
  • Description
    ZINC69391 is a selective inhibitor of Rac1 with antiproliferative and antimetastatic effects. ZINC69391 interferes with the interaction of Rac1 with Dock180, reduces Rac1-GTP levels and induces apoptosis.(In Vitro):In U-87 MG and LN229 cells, ZINC69391 (0-125 μM) reduces cell proliferation of human glioma cells. ZINC69391 (50-100 μM) triggers cell cycle arrest. ZINC69391 inhibits the growth of U937, HL-60, KG1A, and Jurkat cells (IC50s = 41-54 μM). In HL-60, U937, and KG1A cell lines, ZINC69391 (50 μM) triggers an increase in apoptotic cells. In LN229 cells, ZINC69391 (50 and 100 μM) augments the enzymatic activity of caspase 3 and increases the percentage of cells in the sub-G0/G1 phase in a concentration-dependent manner.(In Vivo):In specific pathogen-free female BALB/c inbred mice (bearing F3II cells), ZINC69391 (25 mg/kg; i.p) impairs metastatic lung colonization and reduces by about 60% the formation of total metastatic lung colonies.
  • In Vitro
    ZINC69391 inhibits growth of U937, HL-60, KG1A and Jurkat cells with IC50s ranging from 41 to 54 μM.ZINC69391 (50-100 μM; 24 hours) augments the enzymatic activity of caspase 3 in a concentration dependent manner.ZINC69391 (0-125 μM; 72h) reduces cell proliferation of human glioma cells.ZINC69391 (50-100 μM; 48 hours) triggers cell cycle arrest.ZINC69391 (50 μM; 24 hours) triggers apoptosis on human acute leukemic cells. Cell Proliferation Assay Cell Line:U-87 MG, LN229 cells Concentration:0-125μM Incubation Time:72 hours Result:Reduced cell proliferation in a concentration-dependent manner.Cell Cycle Analysis Cell Line:LN229 cells Concentration:50, 100 μM Incubation Time:48 hours Result:Resulted in a significant increased percentage of cells in the sub-G0/G1 phase in a concentration dependent manner.Apoptosis Analysis Cell Line:HL-60, U937 and KG1A cell lines Concentration:50 μM Incubation Time:24 hours Result:Led to a significant increase in apoptotic cells.
  • In Vivo
    ZINC69391 (25 mg/kg; i.p; daily for 21 days) impairs metastatic lung colonization in a syngeneic animal model. Animal Model:Specific pathogen-free female BALB/c inbred mice (bearing F3II cells)Dosage:25 mg/kg body weight Administration:I.p; daily for 21 days Result:Significantly reduced by about 60% the formation of total metastatic lung colonies.
  • Synonyms
    ZINC-69391 | N'-(4,6-dimethylpyrimidin-2-yl)-N-[2-(trifluoromethyl)phenyl]guanidine
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    EGFR|EGFR (L858R)|EGFR (L858R/T790M)|EGFR (L858R/T790M/C797S)
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    303094-67-9
  • Formula Weight
    309.296
  • Molecular Formula
    C14H14F3N5
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 25 mg/mL (80.83 mM)
  • SMILES
    Cc1cc(C)nc(NC(=N)Nc2ccccc2C(F)(F)F)n1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Zhang H, et al. Discovery of 2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as new EGFR-TKIs. Eur J Med Chem. 2018 Mar 25;148:221-237.
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