Adenosine
| Clinical data | |
|---|---|
| Trade names | Adenocard; Adenocor; Adenic; Adenoco; Adeno-Jec; Adenoscan; Adenosin; Adrekar; Krenosin | 
| Other names | SR-96225 (developmental code name) | 
| AHFS/Drugs.com | Monograph | 
| Pregnancy category | 
 (adenosine may be safe to the fetus in pregnant women) | 
| Routes of administration | Intravenous | 
| ATC code | |
| Physiological data | |
| Source tissues | Primarily liver | 
| Metabolism | Rapidly converted to inosine and adenosine monophosphate | 
| Legal status | |
| Legal status | 
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| Pharmacokinetic data | |
| Bioavailability | Rapidly cleared from circulation via enzyme degradation | 
| Protein binding | No | 
| Metabolism | Rapidly converted to inosine and adenosine monophosphate | 
| Elimination half-life | cleared plasma <30 seconds; half-life <10 seconds | 
| Excretion | can leave cell intact or can be degraded to hypoxanthine, xanthine, and ultimately uric acid | 
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.000.354 | 
| Chemical and physical data | |
| Formula | C10H13N5O4 | 
| Molar mass | 267.245 g·mol−1 | 
| 3D model (JSmol) | |
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| (what is this?) (verify) | |
Adenosine (symbol A) is an organic compound that occurs widely in nature in the form of diverse derivatives. The molecule consists of an adenine attached to a ribose via a β-N9-glycosidic bond. Adenosine is one of the four nucleoside building blocks of RNA (and its derivative deoxyadenosine is a building block of DNA), which are essential for all life on Earth. Its derivatives include the energy carriers adenosine mono-, di-, and triphosphate, also known as AMP/ADP/ATP. Cyclic adenosine monophosphate (cAMP) is pervasive in signal transduction. Adenosine is used as an intravenous medication for some cardiac arrhythmias.
Adenosyl (abbreviated Ado or 5'-dAdo) is the chemical group formed by removal of the 5′-hydroxy (OH) group. It is found in adenosylcobalamin (an active form of vitamin B12) and as a radical in the radical SAM enzymes.