Weight | 161.157 g/mol |
---|---|
Formula | C6H11NO4 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
2-Aminohexanedioic acid (542-32-5)
2-Aminoadipic Acid · alpha-Aminoadipic Acid · 2 Aminohexanedioic Acid
Score:
#1117 in Biochemistry
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#2852 in Biology
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#3570 in Chemistry
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- 2-Aminoadipic acid is a biomarker for diabetes risk (Journal of Clinical Investigation, 2013)
- 2-Aminoadipic acid is a marker of protein carbonyl oxidation in the aging human skin: Effects of diabetes, renal failure and sepsis (Biochemical Journal, 2007)
- Catabolism of lysine in Penicillium chrysogenum leads to formation of 2-aminoadipic acid, a precursor of penicillin biosynthesis (Applied and Environmental Microbiology, 1994)
- A comparison of the effects of isomers of alpha-aminoadipic acid and 2-amino-4-phosphonobutyric acid on the light response of the Muller glial cell and the electroretinogram (Neuroscience, 1984)
- Twenty-four-hour intravenous and oral tracer studies with L-[1-13C]-2-aminoadipic acid and L-[1-13C]lysine as tracers at generous nitrogen and lysine intakes in healthy adults. (The American Journal of Clinical Nutrition, 1998)
- Expression of -amyloid precursor and Bcl-2 proto-oncogene proteins in rat retinas after intravitreal injection of aminoadipic acid (Neurochemistry International, 1999)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-Aminoadipic Acid
- alpha-Aminoadipic Acid
- 2 Aminohexanedioic Acid
- alpha Aminoadipic Acid
- 2 Aminoadipic Acid
-
SMILESC(CC(C(=O)O)N)CC(=O)O
-
InChIKeyOYIFNHCXNCRBQI-UHFFFAOYSA-N
- Pubchem - 2-Aminohexanedioic acid
- Wikipedia - -aminoadipic acid
The -aminoadipate pathway is a biochemical pathway for the synthesis of the amino acid L-lysine. In the eukaryotes, this pathway is unique to the higher fungi (containing chitin in their cell walls) and the euglenids. It has also been reported from bacteria of the genus Thermus.
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