Theophylline monohydrate

CAS No. 5967-84-0

Theophylline monohydrate( —— )

Catalog No. M15215 CAS No. 5967-84-0

A methylxanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervous system stimulant activities.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 34 In Stock
50MG 45 In Stock
100MG 59 In Stock
200MG 106 In Stock
500MG 146 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Theophylline monohydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    A methylxanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervous system stimulant activities.
  • Description
    A methylxanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervous system stimulant activities. Mechanistically, theophylline acts as a phosphodiesterase inhibitor, adenosine receptor blocker, and histone deacetylase activator. Theophylline is marketed under several brand names such as Uniphyl and Theochron, and it is indicated mainly for asthma, bronchospasm, and COPD.(In Vitro):Theophylline (1,3-Dimethylxanthine) (1-1000 μM) inhibits cAMP hydrolysis by PDE in homogenates of bronchial tissue to relax human bronchus and pulmonary arteries.Theophylline (1,3-Dimethylxanthine) (10 μg/mL; 24 h; eosinophils) induces apoptosis through a reduction in the antiapoptotic protein Bcl-2.Theophylline (1,3-Dimethylxanthine) (0-500 μM; 2 h; A549 cells) inhibits NF-κB activation, I kappa B alpha (I-κBα) degradation and decreases the level of IL-6 in a concentration-dependent manner.Theophylline (1,3-Dimethylxanthine) (0-1000 μM; 30 min; A549 cells) induces histone deacetylase activity to decrease inflammatory gene expression.(In Vivo):Theophylline (1,3-Dimethylxanthine) (100 mg/kg; i.p.; daily, for 9 d; male Swiss mice) has anti-inflammatory activity in mice and increases IL-6 and IL-10 levels and inhibits TNF-α and NO.
  • In Vitro
    Theophylline (1,3-Dimethylxanthine) monohydrate (1-1000 μM) inhibits cAMP hydrolysis by PDE in homogenates of bronchial tissue to relax human bronchus and pulmonary arteries.Theophylline (1,3-Dimethylxanthine) monohydrate (10 μg/mL; 24 h; eosinophils) induces apoptosis through a reduction in the antiapoptotic protein Bcl-2.Theophylline (1,3-Dimethylxanthine) monohydrate (0-500 μM; 2 h; A549 cells) inhibits NF-κB activation, I kappa B alpha (I-κBα) degradation and decreases the level of IL-6 in a concentration-dependent manner.Theophylline (1,3-Dimethylxanthine) monohydrate (0-1000 μM; 30 min; A549 cells) induces histone deacetylase activity to decrease inflammatory gene expression. Western Blot Analysis Cell Line:A549 cells Concentration:0, 20, 100 and 500 μM Incubation Time:2 hours Result:Decreased the expression of NF-κB p65 and I-κBα degradation in a concentration-dependent manner.Western Blot Analysis Cell Line:Eosinophils Concentration:10 μg/mL Incubation Time:24 hours Result:Decreased the expression of Bcl-2.
  • In Vivo
    Theophylline (1,3-Dimethylxanthine) (100 mg/kg; i.p.; daily, for 9 d; male Swiss mice) has anti-inflammatory activity in mice and increases IL-6 and IL-10 levels and inhibits TNF-α and NO. Animal Model:Male Swiss mice Dosage:100 mg/kg Administration:Intraperitoneal injection; daily, for 9 daysResult:Increased IL-6 and IL-10 levels and inhibited TNF-α and NO.
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    AChR
  • Recptor
    Adenosine receptor| HDAC2| PDE
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    5967-84-0
  • Formula Weight
    198.18
  • Molecular Formula
    C7H8N4O2·H2O
  • Purity
    >98% (HPLC)
  • Solubility
    Soluble in Water
  • SMILES
    O.CN1C2=C(NC=N2)C(=O)N(C)C1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Nantwi KD, et al. J Spinal Cord Med. 2003 Winter;26(4):364-7
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