QTX125

CAS No. 1279698-31-5

QTX125( QTX 125 | QTX-125 )

Catalog No. M11154 CAS No. 1279698-31-5

QTX125 (QTX-125) is a novel potent, selective HDAC6 inhibitor, displays excellent selectivity over other HDACs.

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    QTX125
  • Note
    Research use only, not for human use.
  • Brief Description
    QTX125 (QTX-125) is a novel potent, selective HDAC6 inhibitor, displays excellent selectivity over other HDACs.
  • Description
    QTX125 (QTX-125) is a novel potent, selective HDAC6 inhibitor, displays excellent selectivity over other HDACs; strongly reduces cell viability with IC50 values of 0.120 and 0.182 uM in two primary samples obtained from patients with MCL; causes cell-growth inhibition and programmed cell death in association with increased levels of acetylated α-tubulin, also antitumoral effect is particularly evident in MCL models, both in culture and in vivo, surpassing the efficacy of currently available HDAC6 inhibitors.
  • In Vitro
    QTX125 (25-500 nM; 24-48 hours) treatment induces the subsequent apoptosis demonstrated by annexin V/propidium iodide double staining and the cleavage of caspase-9, caspase-8, caspase-3, and PARP. In MCL cell lines MINO, REC-1, IRM-2 and HBL-2 cells, QTX125 (10 nM, 10 μM, 100 μM) induces dose-dependent hyperacetylation of α-tubulin.QTX125 has the strongest growth-inhibitory effect in Burkitt cell lymphoma, follicular lymphoma, and mantle cell lymphoma (MCL). Apoptosis Analysis Cell Line:MINO, REC-1, IRM-2 and HBL-2 cells Concentration:25 nM, 50 nM, 100 nM, 500 nM Incubation Time:24 hours, 48 hours Result:Inhibited annexin V/propidium iodide double staining.Western Blot Analysis Cell Line:MINO, REC-1, IRM-2 and HBL-2 cells Concentration:25 nM, 50 nM, 100 nM, 500 nM Incubation Time:24 hours Result:Inhibited the cleavage of caspase-9, caspase-8, caspase-3, and PARP.
  • In Vivo
    QTX125 (60 mg/kg; i.p.; daily dosing for 5 days; for 4 weeks) treatment inhibits tumor growth in REC-1 or MINO cells xenografted in nude mice. Animal Model:Nude mice bearing REC-1 or MINO cells Dosage:60 mg/kg Administration:Intraperitoneal administration; daily dosing for 5 days; for 4 weeks Result:Inhibited tumor growth in REC-1 or MINO cells xenografted in nude mice.
  • Synonyms
    QTX 125 | QTX-125
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1279698-31-5
  • Formula Weight
    417.421
  • Molecular Formula
    C23H19N3O5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(C1=C(C2=COC=C2)C=C(C3=CC=C(O)C=C3)N1)NCC4=CC=C(C(NO)=O)C=C4
  • Chemical Name
    3-(3-furyl)-N-{4-[(hydroxyamino)carbonyl]benzyl}-5-(4-hydroxyphenyl)-1H-pyrrole2-carboxamide

Shipping & Storage Information

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

Reference

1. Perez-Salvia M, et al. Haematologica. 2018 Jun 7. pii: haematol.2018.189241.
molnova catalog
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