Theophylline
CAS No. 58-55-9
Theophylline( 1,3-Dimethylxanthine | NSC 2066 )
Catalog No. M15151 CAS No. 58-55-9
Theophylline is a methylated xanthine derivative; competitive nonselective phosphodiesterase inhibitor and nonselective adenosine receptor antagonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameTheophylline
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NoteResearch use only, not for human use.
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Brief DescriptionTheophylline is a methylated xanthine derivative; competitive nonselective phosphodiesterase inhibitor and nonselective adenosine receptor antagonist.
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DescriptionTheophylline is a methylated xanthine derivative; competitive nonselective phosphodiesterase inhibitor and nonselective adenosine receptor antagonist.(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.
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In Vitro——
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In Vivo——
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Synonyms1,3-Dimethylxanthine | NSC 2066
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PathwayEndocrinology/Hormones
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TargetAChR
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RecptorAdenosine receptor| HDAC2| PDE
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Research AreaOther Indications
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Indication——
Chemical Information
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CAS Number58-55-9
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Formula Weight180.16
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Molecular FormulaC7H8N4O2
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Purity>98% (HPLC)
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Solubilitysoluble in Water
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SMILESCN1C2=C(NC=N2)C(=O)N(C)C1=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Philipp S, et al. Cardiovasc Res. 2006 May 1;70(2):308-14.
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