Structure via PubChem · Public domain (PubChem)
aminocaproic acid
Sign in to saveAlso known as ε-aminocaproic acid, Amicar®, EACA, 6-aminohexanoic acid
chemical compound
Chemical data
- Formula
- C6H13NO2
- Molecular weight
- 131.17 g/mol
- IUPAC name
- 6-azaniumylhexanoate
- SMILES
- C(CCC(=O)[O-])CC[NH3+]
- InChIKey
- SLXKOJJOQWFEFD-UHFFFAOYSA-N
- XLogP
- -2.3
- Polar surface area
- 67.8 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 1964
- Admin. routes
- oral, parenteral
- Indications
- hemorrhage, aortic disease, rosacea, inflammation
via ChEMBL · EBI
Research
6,140 papers- AMINOCAPROIC ACID, AN INHIBITOR OF FIBRINOLYSIS.The American journal of the medical sciences · 1965
- EPSILON-AMINOCAPROIC ACID AND OTHER INHIBITORS OF FIBRINOLYSIS.British medical bulletin · 1964
- Epsilon-aminocaproic acid (EACA).Seminars in thrombosis and hemostasis · 1978
- PATHOLOGICAL FIBRINOLYSIS.British medical bulletin · 1964
- Epsilon aminocaproic acid in hemophiliacs undergoing dental extractions: a concise review.Oral surgery, oral medicine, and oral pathology · 1981
via PubMed
Wikidata facts
- Has part
- carbon
- Mass
- 131.095
- Manufacturer
- Pfizer
- Has use
- medication
Show 10 more facts
- medical condition treated
- bleeding
- Commons category
- Aminocaproic acid
- chemical formula
- C₆H₁₃NO₂
- route of administration
- topical medication
- canonical SMILES
- C(CCC(=O)O)CCN
- World Health Organisation international non-proprietary name
- aminocaproic acid
- subject has role
- antifibrinolytic
- physically interacts with
- Plasminogen activator, tissue type
- melting point
- 211
- found in taxon
- Caenorhabditis elegans
via Wikidata · CC0