Weight | 131.175 g/mol |
---|---|
Formula | C6H13NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
6-aminohexanoic acid (1319-82-0, 60-32-2)
Aminocaproic Acid · Amicar · epsilon Aminocaproic Acid
Score:
#719 in Biochemistry
,
#859 in Physics
,
#1996 in Biology
,
#2435 in Chemistry
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- xi-Aminocaproic acid: an inhibitor of plasminogen activation. (Journal of Biological Chemistry, 1959)
- Epsilon aminocaproic acid therapy of hereditary angioneurotic edema. A double-blind study. (The New England Journal of Medicine, 1972)
- Epsilon-aminocaproic Acid for Treatment of Fibrinolysis during Liver Transplantation (Anesthesiology, 1987)
- Is -aminocaproic acid as effective as aprotinin in reducing bleeding with cardiac surgery? A meta-analysis (Circulation, 1999)
- Tranexamic Acid Reduces Red Cell Transfusion Better than -aminocaproic Acid or Placebo in Liver Transplantation (Anesthesia & Analgesia, 2000)
- Quantitative determination of the binding of epsilon-aminocaproic acid to native plasminogen. (Journal of Biological Chemistry, 1978)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Aminocaproic Acid
- Amicar
- epsilon Aminocaproic Acid
- Caprolest
- 6 Aminocaproic Acid
- 6 Aminohexanoic Acid
- CY116
- CY 116
- Caprocid
- Epsamon
- Capralense
- Epsikapron
- Hexalense
- Hemocaprol
- 6-Aminocaproic Acid
- CY-116
- epsilon-Aminocaproic Acid
- Caproamin
- Capramol
-
SMILESC(CCC(=O)O)CCN
-
InChIKeySLXKOJJOQWFEFD-UHFFFAOYSA-N
- Pubchem - 6-aminohexanoic acid
- Wikipedia - aminocaproic acid
Aminocaproic acid (also known as -aminocaproic acid, -Ahx, or 6-aminohexanoic acid) is a derivative and analogue of the amino acid lysine, which makes it an effective inhibitor for enzymes that bind that particular residue. Such enzymes include proteolytic enzymes like plasmin, the enzyme responsible for fibrinolysis. For this reason it is effective in treatment of certain bleeding disorders, and it is marketed as Amicar.
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