Theobromine

CAS No. 83-67-0

Theobromine( Diurobromine | NSC 5039 | SC-15090 )

Catalog No. M16101 CAS No. 83-67-0

3,7-Dimethylxanthine. The principle alkaloid in Theobroma cacao (the cacao bean) and other plants.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Theobromine
  • Note
    Research use only, not for human use.
  • Brief Description
    3,7-Dimethylxanthine. The principle alkaloid in Theobroma cacao (the cacao bean) and other plants.
  • Description
    3,7-Dimethylxanthine. The principle alkaloid in Theobroma cacao (the cacao bean) and other plants. A xanthine alkaloid that is used as a bronchodilator and as a vasodilator. It has a weaker diuretic activity than THEOPHYLLINE and is also a less powerful stimulant of smooth muscle. It has practically no stimulant effect on the central nervous system. It was formerly used as a diuretic and in the treatment of angina pectoris and hypertension. (In Vitro):Theobromine, at concentrations above 25 μM, decreases lipid accumulation in these cells. Cell viability is not affected by Theobromine. Theobromine, at concentrations above 25 μM, suppresses protein expression of PPARγ, C/EBPα and adipogenic genes. The mRNA levels of these genes are also decreased by Theobromine.(In Vivo):Body weights are lower in the Theobromine group than in the vehicle group. In addition, Theobromine suppresses gains in weight of epididymal and perirenal adipose tissues. The mean adipocyte area is smaller in the Theobromine group than in the vehicle group. Theobromine group shows lower counts than the other groups when considering the number of bacteria per fecal weight (p=0.021 and p=0.055 compare to the reference (RF) and the cocoa (CC) groups, respectively). The Theobromine diet leads to higher pH values than those found after the RF and CC diets. Fecal concentrations of lactic acid are not signi?cantly affected by the experimental diets (4.26±1.54 mM in RF group; 1.96±0.41 mM in CC group; 2.69±0.73 mM in Theobromine group).
  • In Vitro
    Theobromine, at concentrations above 25 μM, decreases lipid accumulation in these cells. Cell viability is not affected by Theobromine. Theobromine, at concentrations above 25 μM, suppresses protein expression of PPARγ, C/EBPα and adipogenic genes. The mRNA levels of these genes are also decreased by Theobromine.
  • In Vivo
    Body weights are lower in the Theobromine group than in the vehicle group. In addition, Theobromine suppresses gains in weight of epididymal and perirenal adipose tissues. The mean adipocyte area is smaller in the Theobromine group than in the vehicle group. Theobromine group shows lower counts than the other groups when considering the number of bacteria per fecal weight (p=0.021 and p=0.055 compare to the reference (RF) and the cocoa (CC) groups, respectively). The Theobromine diet leads to higher pH values than those found after the RF and CC diets. Fecal concentrations of lactic acid are not signi?cantly affected by the experimental diets (4.26±1.54 mM in RF group; 1.96±0.41 mM in CC group; 2.69±0.73 mM in Theobromine group).
  • Synonyms
    Diurobromine | NSC 5039 | SC-15090
  • Pathway
    Endocrinology/Hormones
  • Target
    AChR
  • Recptor
    Adenosine receptor| PDE
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    83-67-0
  • Formula Weight
    180.16
  • Molecular Formula
    C7H8N4O2
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 330 mg/L
  • SMILES
    O=C(N1)N(C)C2=C(N(C)C=N2)C1=O
  • Chemical Name
    3,7-dimethyl-1H-purine-2,6-dione

Shipping & Storage Information

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

Reference

1.Chou CC, Vickroy TW. Am J Vet Res. 2003 Feb;64(2):216-24.
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