L-Aspartic Acid

Chemical compound
trends
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instance of
Medication
chemical structure
alias
L-Asp
L-aspartate
(S)-2-aminobutanedioic acid
(S)-2-aminosuccinic acid
(2S)-2-aminobutanedioic acid
(2S)-2-aminosuccinic acid
(2S)-Aspartate
L-Aminosuccinic acid
L-Asparaginic acid
(S)-(+)-Aspartic acid
(+)-Aspartate
(S)-Aspartate
2-Aminosuccinate
alpha-Aminosuccinic acid
(+)-Aspartic acid
alpha-Aminosuccinate
L-Asparaginate
(S)-amino-Butanedioate
Asparagic acid
L-(+)-Aspartic acid
(L)-Aspartic acid
Asparatate
2-Amino-3-methylsuccinate
(R)-2-aminosuccinate
L-Asparagic acid
(S)-Aminobutanedioate
(S)-Aspartic acid
(2S)-Aspartic acid
(S)-amino-Butanedioic acid
Aminosuccinate
Asparagate
(S)-(+)-Aspartate
L-Asparagate
(S)-Aminobutanedioic acid
L-(+)-Aspartate
Asparaginate
H-Asp-OH
(S)-2-aminosuccinate
(L)-Aspartate
2-Amino-3-methylsuccinic acid
L-Aminosuccinate
Aspartate
Asparaginic acid
2-Aminosuccinic acid
Asp
Aspartic acid
D
L-Asparaginsaeure
L-Asparaginsäure
L-Aspartic acid
L-Aspartate
L-Aspartic Acid
ASP
material used
N-Acetyl-l-Aspartate
mass
133.038 dalton
chemical formula
C₄H₇NO₄
physically interacts with
Glutamate Ionotropic Receptor NMDA…
Glutamate Ionotropic Receptor NMDA…
Glutamate Ionotropic Receptor NMDA…
Glutamate Ionotropic Receptor NMDA…
Glutamate Ionotropic Receptor NMDA…
media
canonical SMILES
C(C(C(=O)O)N)C(=O)O
isomeric SMILES
N[C@@H](CC(O)=O)C(O)=O
NCI Thesaurus ID
C29608
World Health Organisation International Nonproprietary Name
aspartic acid (english)
Commons category
Aspartic acid
Wikimedia Commons URL
Wikipedia creation date
7/22/2002
Wikipedia incoming links count
Wikipedia opening text
Aspartic acid (symbol Asp or D; the ionic form is known as aspartate), is an α-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 α-amino group is in the protonated –NH+ 3 form under physiological conditions, while its α-carboxylic acid group is deprotonated −COO− under physiological conditions. Aspartic acid has an acidic side chain (CH2COOH) which reacts with other amino acids, enzymes and proteins in the body. Under physiological conditions (pH 7.4) in proteins the side chain usually occurs as the negatively charged aspartate form, −COO−. It is a non-essential amino acid in humans, meaning the body can synthesize it as needed. It is encoded by the codons GAU and GAC. D-Aspartate is one of two D-amino acids commonly found in mammals.[3] In proteins aspartate sidechains are often hydrogen bonded to form asx turns or asx motifs, which frequently occur at the N-termini of alpha helices. The L-isomer of Asp is one of the 22 proteinogenic amino acids, i.e., the building blocks of proteins. Aspartic acid, like glutamic acid, is classified as an acidic amino acid, with a pKa of 3.9, however in a peptide this is highly dependent on the local environment, and could be as high as 14. Asp is pervasive in biosynthesis. Because aspartate can be synthesized by the body it is classified as a non-essential amino acid.
Wikipedia redirect
Aspartate
Asparagine acid
Aspartic Acid
1-Aspartic Acid
L-Aspartic Acid
Calcium aspartate
D-aspartic acid
HO2CCH(NH2)CH2CO2H
L-aspartate
D-aspartate
Asparaginic acid
Asparate
Aspatofort
Aspartyl
Asparagic acid
HOOCCH(NH2)CH2COOH
Aspartic
Aspartic acid metabolism
Aminosuccinic acid
L-aspartic acid
Wikipedia URL
AICS Chemical ID
CAS Registry Number
ChEBI ID
ChEMBL ID
ChemSpider ID
CosIng number
DrugBank ID
EC number
200-291-6
ECHA InfoCard ID
Freebase ID
Gmelin number
3333
GND ID
Gran Enciclopèdia Catalana ID
Great Russian Encyclopedia Online ID
Guide to Pharmacology Ligand ID
Human Metabolome Database ID
InChI
InChIKey
KEGG ID
KNApSAcK ID
Library of Congress authority ID
NDF-RT ID
NSC number
PubChem CID
Quora topic ID
Reaxys registry number
1723530
RxNorm ID
SPLASH
UNII
WikiSkripta ID
ZVG number
external links