L-2-Aminobutanedioic acid
L-2-Aminobutanedioic acid Brand names, L-2-Aminobutanedioic acid Analogs
- (+)-Aspartic acid
- (2S)-Aspartic acid
- (L)-ASPARTIC ACID
- (S)-Aminobutanedioic acid
- (S)-Aspartic acid
- 4-04-00-02998 (Beilstein Handbook Reference)
- AI3-04461
- Acide aspartique [INN-French]
- Acido aspartico [INN-Spanish]
- Acidum asparticum
- Acidum asparticum [INN-Latin]
- Aminosuccinic acid
- Asparagic acid
- Asparagic acid (VAN)
- Asparaginic acid
- Asparaginic acid (VAN)
- Asparaginsaeure [German]
- Aspartate
- Aspartate, L-
- Aspartic Acid [USAN:INN]
- Aspartic acid
- Aspartic acid (VAN)
- Aspartic acid, L-
- Aspatofort
- BRN 1723530
- Butanedioic acid, amino-, (S)-
- CCRIs 6181
- EINECS 200-291-6
- FEMA No. 3565
- H-Asp-OH
- HSDB 1430
- L( )-Aminobernsteinsaeure
- L-(+)-Aspartic acid
- L-2-Aminobutanedioic acid
- L-Aminosuccinic acid
- L-Asparagic acid
- L-Asparaginic acid
- L-Asparaginsaeure
- L-Asparaginsyra
- L-Aspartic acid
- L-Aspartinsaeure
- NSC 3973
L-2-Aminobutanedioic acid Brand Names Mixture
- No information avaliable
L-2-Aminobutanedioic acid Chemical_Formula
C4H7N1O4
L-2-Aminobutanedioic acid RX_link
No information avaliable
L-2-Aminobutanedioic acid fda sheet
L-2-Aminobutanedioic acid msds (material safety sheet)
L-2-Aminobutanedioic acid Synthesis Reference
No information avaliable
L-2-Aminobutanedioic acid Molecular Weight
133.104 g/mol
L-2-Aminobutanedioic acid Melting Point
230 oC
L-2-Aminobutanedioic acid H2O Solubility
4.5 g/l
L-2-Aminobutanedioic acid State
Solid
L-2-Aminobutanedioic acid LogP
-0.67 +/- 0.36
L-2-Aminobutanedioic acid Dosage Forms
Capsules and powder
L-2-Aminobutanedioic acid Indication
There is no support for the claim that aspartates are exercise performance enhancers, i.e. ergogenic aids.
L-2-Aminobutanedioic acid Pharmacology
L-aspartate is considered a non-essential amino acid, meaning that, under normal physiological conditions, sufficient amounts of the amino acid are synthesized in the body to meet the body's requirements. L-aspartate is formed by the transamination of the Krebs cycle intermediate oxaloacetate. The amino acid serves as a precursor for synthesis of proteins, oligopeptides, purines, pyrimidines, nucleic acids and L-arginine. L-aspartate is a glycogenic amino acid, and it can also promote energy production via its metabolism in the Krebs cycle. These latter activities were the rationale for the claim that supplemental aspartate has an anti-fatigue effect on skeletal muscle, a claim that was never confirmed.
L-2-Aminobutanedioic acid Absorption
Absorbed from the small intestine by an active transport process
L-2-Aminobutanedioic acid side effects and Toxicity
Mild gastrointestinal side effects including diarrhea. LD50 (rat) > 5,000 mg/kg.
L-2-Aminobutanedioic acid Patient Information
No information avaliable
L-2-Aminobutanedioic acid Organisms Affected
Humans and other mammals
