Aspirin, also known as acetylsalicylic acid (ASA), is a medication, often used to treat pain, fever, and inflammation.[2] Aspirin is also used long-term, at low doses, to help prevent heart attacks, strokes, and blood clot formation in people at high risk of developing blood clots.[3] Low doses of aspirin may be given immediately after a heart attack to reduce the risk of another heart attack or the death of heart tissue.[4][5] Aspirin may be effective at preventing certain types of cancer, particularly colorectal cancer.[6][7][8]
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2-(acetoxy)benzoic acid |
Pronunciation | acetylsalicylic acid /əˌsiːtəlˌsælᵻˈsɪlᵻk/ |
AHFS/Drugs.com | monograph |
MedlinePlus | a682878 |
Pregnancy category |
AU: C US: C (Risk not ruled out) D in the 3rd trimester |
Legal status |
AU: S2 (Pharmacy only) except when given intravenously (in which case it is schedule 4), used in animal medicine (schedule 5/6) or when the dose is higher than usual. UK: General sales list (GSL, OTC) US: OTC |
Routes of administration |
Most commonly oral, also rectal, lysine acetylsalicylate may be given intravenously or intramuscularly |
Bioavailability | 80–100%[1] |
Protein binding | 80–90%[2] |
Metabolism | Hepatic, (CYP2C19 and possibly CYP3A), some is also hydrolysed to salicylate in the gut wall.[2] |
Biological half-life | Dose-dependent; 2–3 hours for low doses, 15–30 hours for large doses.[2] |
Excretion | Urine (80–100%), sweat, saliva, feces[1] |
CAS Number | 50-78-2 |
ATC code | A01AD05 B01AC06, N02BA01 |
PubChem | CID: 2244 |
IUPHAR/BPS | 4139 |
DrugBank | DB00945 |
ChemSpider | 2157 |
UNII | R16CO5Y76E |
KEGG | D00109 |
ChEBI | CHEBI:15365 |
ChEMBL | CHEMBL25 |
Synonyms | 2-acetoxybenzoic acid acetylsalicylate acetylsalicylic acid O-acetylsalicylic acid |
PDB ligand ID | AIN (PDBe, RCSB PDB) |
Formula | C9H8O4 |
Molecular mass | 180.157 g/mol |
SMILES[show] |
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InChI[show] |
Density | 1.40 g/cm3 |
Melting point | 135 °C (275 °F) |
Boiling point | 140 °C (284 °F) (decomposes) |
Solubility in water | 3 mg/mL (20 °C) |