Chemistry Reference and  Research
           
 
Periodic Table
- standard table
- large table
 
Chemical Elements
- by name
- by symbol
- by atomic number
 
Chemical Properties
 
Chemical Reactions
 
Organic Chemistry
 
Branches of Chemistry
Analytical chemistry
Biochemistry
Computational Chemistry
Electrochemistry
Environmental chemistry
Geochemistry
Inorganic chemistry
Materials science
Medicinal chemistry
Nuclear chemistry
Organic chemistry
Pharmacology
Physical chemistry
Polymer chemistry
Supramolecular Chemistry
Thermochemistry

Theobromine

Theobromine chemical structure
Theobromine

3,7-dihydro-3,7-dimethyl-1H-purine-2,6-dione
CAS number
83-67-0
ATC code
C03BD01 and R03DA07
Chemical formula C7H8N4O2
Molecular weight 180.166
Bioavailability  ?
Metabolism  ?
Elimination half-life  ?
Excretion  ?
Pregnancy category  ?
Legal status Uncontrolled substance
Routes of administration  ?

Theobromine is a bitter alkaloid of the methylxanthine family, which also includes the similar compounds theophylline and caffeine. It is known to induce mutations in bacteria and lower eukaryotes, but does not seem to cause mutations in higher eukaryotes, such as humans.

Theobromine is a chemical stimulant frequently confused with caffeine, but has very different effects on the human body. It is a mild, lasting stimulant with a mood improving effect. In medicine, it is used as a diuretic, vasodilator, and myocardial stimulant.

Theobromine is the primary alkaloid found in cocoa and chocolate (Theobroma cacao is the scientific name of the cacao tree). Its presence is one of the causes for chocolate's mood-elevating effects. In chocolate, theobromine exists in doses that are safe for humans to consume in large quantities, but can be lethal for animals such as dogs and horses, as they metabolize theobromine more slowly.

Scientists have recently discovered that theobromine has an antitussive effect superior to codeine by suppressing vagus nerve activity. [1]

Alternate names are: Riddospas, Riddovydrin, Santheose, Seominal, Theobrominum, Theoguardenal, Theominal and Théoxalvose.

External links

01-04-2007 01:16:19
The contents of this article are licensed from Wikipedia.org under the GNU Free Documentation License. How to see transparent copy