345938
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
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
98%
Form:
solid
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)
SMILES string
OC(=O)CC(NC(=O)Cc1c[nH]c2ccccc12)C(O)=O
InChI key
VAFNMNRKDDAKRM-UHFFFAOYSA-N
assay
98%
form
solid
mp
198 °C (dec.) (lit.)
Quality Level
General description
N-(3-Indolylacetyl)-DL-aspartic acid is an indole derivative.
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.
- Building block in coordination chemistry with platinum and palladium ions
Storage Class
13 - Non Combustible Solids
wgk
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
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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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