CHEBI:21484 - N-(indole-3-acetyl)-L-aspartic acid

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ChEBI Name N-(indole-3-acetyl)-L-aspartic acid
ChEBI ID CHEBI:21484
ChEBI ASCII Name N-(indole-3-acetyl)-L-aspartic acid
Definition An N-acyl-L-aspartic acid in which the acyl group is specified as indole-3-acetyl.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via indoleacetic acid conjugate )
Related Structures
N-(indole-3-acetyl)-L-aspartic acid is a Structural Derivative of
indole-3-acetic acid
Mass : 175.18400
Formula : C10H9NO2
16411
indole-3-acetic acid
Mass : 175.18400
Formula : C10H9NO2
16411
L-aspartic acid
Mass : 133.10270
Formula : C4H7NO4 C4H7NO4
17053
proteinogenic amino acid
Definition : Any of the 23 alpha-amino acids that are precursors to proteins, and are incorporated into proteins during translation. The group includes the 20 amino acids encoded by the nuclear genes of eukaryotes together with selenocysteine, pyrrolysine, and N-formylmethionine. Apart from glycine, which is non-chiral, all have L configuration.
L-alpha-amino acid
Mass : 74.05870
Formula : C2H4NO2R
15705
amino acid
Definition : A carboxylic acid containing one or more amino groups.
N-(indole-3-acetyl)-L-aspartic acid is a Conjugate Acid of
N-(indole-3-acetyl)-L-aspartate(2-)
Mass : 288.256
Formula : C14H12N2O5
133482
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