| Weight | 133.103 g/mol |
|---|---|
| Formula | C4H7NO4 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
D-Aspartic acid (1783-96-6)
D Aspartate · D Aspartic Acid · D-Aspartate
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#639 in Neuroscience
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- Selective impairment of learning and blockade of long-term potentiation by an N-methyl-D-aspartate receptor antagonist, AP5 (Nature, 1986)
- Apoptosis and necrosis: two distinct events induced, respectively, by mild and intense insults with N-methyl-D-aspartate or nitric oxide/superoxide in cortical cell cultures (Proceedings of the National Academy of Sciences of the United States of America, 1995)
- The induction and maintenance of central sensitization is dependent on N-methyl-d-aspartic acid receptor activation; implications for the treatment of post-injury pain hypersensitivity states (Pain, 1991)
- A Randomized Trial of an N-methyl-D-aspartate Antagonist in Treatment-Resistant Major Depression (Archives of General Psychiatry, 2006)
- Blockade of N-methyl-D-aspartate receptors may protect against ischemic damage in the brain (Science, 1984)
- The anticonvulsant MK-801 is a potent N-methyl-D-aspartate antagonist. (Proceedings of the National Academy of Sciences of the United States of America, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - D Aspartate
- D Aspartic Acid
- D-Aspartate
- 3-hydroxy-N-(2-methyl-1-oxo-2-propenyl)-
-
SMILESC(C(C(=O)O)N)C(=O)O
-
InChIKeyCKLJMWTZIZZHCS-UHFFFAOYSA-N
- Pubchem - D-Aspartic acid
- Wikipedia - D-aspartic acid
Aspartic acid (abbreviated as Asp or D; encoded by the codons [GAU and GAC]), also known as aspartate, is an -amino acid that is used in the biosynthesis of proteins. Similar to all other amino acids it contains an amino group and a carboxylic acid. Its -amino group is in the protonated NH+ 3 form under physiological conditions, while its -carboxylic acid group is deprotonated COO under physiological conditions.
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D-Aspartic acid
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