Proflavine Hemisulfate

CAS No. 1811-28-5

Proflavine Hemisulfate( Proflavine hemisulfate | Proflavine hemisulphate | EINECS 217-320-3 )

Catalog No. M12778 CAS No. 1811-28-5

Proflavine Hemisulfate is a topical antiseptic by interchelating DNA, thereby disrupting DNA synthesis and leading to high levels of mutation in the copied DNA strands.

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    Proflavine Hemisulfate
  • Note
    Research use only, not for human use.
  • Brief Description
    Proflavine Hemisulfate is a topical antiseptic by interchelating DNA, thereby disrupting DNA synthesis and leading to high levels of mutation in the copied DNA strands.
  • Description
    Proflavine Hemisulfate is a topical antiseptic by interchelating DNA, thereby disrupting DNA synthesis and leading to high levels of mutation in the copied DNA strands.(In Vitro):Proflavine (0.1-10 μM; 24 hours) inhibits the growth of Kir3.2-transformant cells and Kir3.2 activity in a concentration-dependent manner.Proflavine (300 μM) progressively reduces the current amplitude of Kir3.2 mutant to 27.7±4.3% of the control.(In Vivo):Proflavine (0.1-10 μM; 24 hours) inhibits the growth of Kir3.2-transformant cells and Kir3.2 activity in a concentration-dependent manner.Proflavine (300 μM) progressively reduces the current amplitude of Kir3.2 mutant to 27.7±4.3% of the control.
  • In Vitro
    Proflavine (0.1-10 μM; 24 hours) inhibits the growth of Kir3.2-transformant cells and Kir3.2 activity in a concentration-dependent manner. Proflavine (300 μM) progressively reduces the current amplitude of Kir3.2 mutant to 27.7±4.3% of the control. Cell Viability AssayCell Line:Kir3.2*-transformant BYT123 cells Concentration:0.1, 1, and 10 μM Incubation Time:24 hours Result:Dose-dependent inhibition of the growth of Kir3.2*-transformant cells. Attenuated the growth of Kir3.2*-transformant cells without affecting the growth of control cells.
  • In Vivo
    The concentrations of Proflavine (20 mg/kg) in whole blood after intravenous injection decreased rapidly at the beginning and remained stable from around 30 min after dosing. Animal Model:Adult male Sprague Dawley rats (weighing approximately 200 g) Dosage:20 mg/kg (Pharmacokinetic Analysis) Administration:Intravenous injection; 2, 4, 5, 10, 15, 20, 25, and 30 min after dosing Result:Concentration decreased rapidly from whole blood in the first 5 min after dosing, followed by a slower decrease.
  • Synonyms
    Proflavine hemisulfate | Proflavine hemisulphate | EINECS 217-320-3
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    DNA/RNA Synthesis
  • Recptor
    DNA mutation| LfrR| QacR| Thrombin
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    1811-28-5
  • Formula Weight
    516.57
  • Molecular Formula
    C26H24N604S
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 22 mg/mL (85.18 mM)
  • SMILES
    C1=CC(=CC2=NC3=C(C=CC(=C3)[NH3+])C=C21)N.C1=CC(=CC2=NC3=C(C=CC(=C3)[NH3+])C=C21)N.[O-]S(=O)(=O)[O-]
  • Chemical Name
    (6-aminoacridin-3-yl)azanium;sulfate

Shipping & Storage Information

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

Reference

1.Stokowa K, et al. J Inorg Biochem, 2012, 106(1), 111-116.
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