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Sigma-Aldrich

N-(3-Indolylacetyl)-DL-aspartic acid

98%

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About This Item

Empirical Formula (Hill Notation):
C14H14N2O5
CAS Number:
Molecular Weight:
290.27
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Quality Level

assay

98%

form

solid

mp

198 °C (dec.) (lit.)

SMILES string

OC(=O)CC(NC(=O)Cc1c[nH]c2ccccc12)C(O)=O

InChI

1S/C14H14N2O5/c17-12(16-11(14(20)21)6-13(18)19)5-8-7-15-10-4-2-1-3-9(8)10/h1-4,7,11,15H,5-6H2,(H,16,17)(H,18,19)(H,20,21)

InChI key

VAFNMNRKDDAKRM-UHFFFAOYSA-N

General description

N-(3-Indolylacetyl)-DL-aspartic acid is an indole derivative.[1]

Application

N-(3-Indolylacetyl)-DL-aspartic acid was used as ligand to investigate the reversible coordination of various indole derivatives to platinum(II) and palladium(II) and spectroscopic, kinetic and mechanistic study of their complexes has been reported.[1]
  • Building block in coordination chemistry with platinum and palladium ions

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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N V Kaminskaia et al.
Inorganic chemistry, 39(22), 5004-5013 (2001-03-10)
Binding of tryptophan residue to intrinsic metal ions in proteins is unknown, and very little is known about the coordinating abilities of indole. Indole-3-acetamide displaces the solvent ligands from cis-[Pt(en)(sol)2]2+, in which sol is acetone or H2O, in acetone solution
Dongbin Xu et al.
Molecular biology reports, 47(6), 4495-4506 (2020-05-24)
The GH3 genes play vital roles in auxin homeostasis by conjugating excess auxin to amino acids. However, how GH3 genes function during grafting in Chinese hickory (Carya cathayensis) is largely unknown. Here, based on the transcriptome database, a comprehensive identification
Hua Li et al.
Journal of chromatography. A, 1583, 80-87 (2018-11-26)
Modified metabolites play important roles in diagnostic monitoring, oxidative response and physiological regulation. Comprehensive analytical methods are greatly needed for improving the coverage of modified metabolites and studying their physiological function. Here, a novel nontargeted profiling method for mapping modified
João Daniel Santos Fernandes et al.
PloS one, 10(7), e0132369-e0132369 (2015-07-15)
Metabolic diversity is an important factor during microbial adaptation to different environments. Among metabolic processes, amino acid biosynthesis has been demonstrated to be relevant for survival for many microbial pathogens, whereas the association between pathogenesis and amino acid uptake and

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