CAS 2456-73-7

Indole-3-acetyl-L-aspartic acid

Description:

Indole-3-acetyl-L-aspartic acid, commonly referred to as IAAsp, is a naturally occurring compound that belongs to the class of amino acids and is a derivative of indole. It features an indole ring structure, which is a bicyclic compound composed of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound is characterized by its role in plant physiology, particularly in the regulation of growth and development, as it is involved in the biosynthesis of auxins, which are essential plant hormones. IAAsp exhibits solubility in water and is typically stable under physiological conditions. Its structure includes an acetyl group attached to the indole moiety and an aspartic acid backbone, contributing to its biological activity. The compound has garnered interest in research for its potential applications in agriculture and plant biotechnology, as well as its implications in understanding plant signaling pathways. Overall, IAAsp represents a significant intersection of biochemistry and plant science, highlighting the intricate relationships between amino acids and plant hormones.

Formula: C₁₄H₁₄N₂O₅

InChI: InChI=1/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: InChIKey=VAFNMNRKDDAKRM-NSHDSACASA-N

SMILES: C(C(N[C@@H](CC(O)=O)C(O)=O)=O)C=1C=2C(NC1)=CC=CC2

Synonyms:

• (2S)-2-[2-(1H-Indol-3-yl)acetamido]butanedioic acid
• (Indole-3-acetyl)aspartic acid
• (Indoleacetyl)aspartic acid
• (S)-2-(2-(1H-Indol-3-yl)acetamido)succinic acid
• 3-Indolylacetyl-<span class="text-smallcaps">L</span>-aspartic acid
• <span class="text-smallcaps">L</span>-Aspartic acid, N-(1H-indol-3-ylacetyl)-
• <span class="text-smallcaps">L</span>-Aspartic acid, N-[2-(1H-indol-3-yl)acetyl]-
• <span class="text-smallcaps">L</span>-Aspartic acid, N-indol-3-ylacetyl-
• Aspartic acid, N-(indol-3-ylacetyl)-
• Aspartic acid, N-(indol-3-ylacetyl)-, <span class="text-smallcaps">L</span>-
• Iaasp
• Indol-3-ylacetylaspartic acid
• Indole-3-acetyl-<span class="text-smallcaps">L</span>-aspartic acid
• Indole-3-acetylasparaginic acid
• Indoleacetylaspartate
• Indolyl-3-aspartic acid
• L-Aspartic acid, N-(1H-indol-3-ylacetyl)-
• N-(1H-indol-3-ylacetyl)-L-aspartic acid
• N-(1H-indol-3-ylacetyl)aspartic acid
• N-(Indole-3-acetyl)aspartic acid
• N-[2-(1H-Indol-3-yl)acetyl]-<span class="text-smallcaps">L</span>-aspartic acid
• Aspartic acid, N-(indol-3-ylacetyl)-, L-
• L-Aspartic acid, N-indol-3-ylacetyl-
• L-Aspartic acid, N-[2-(1H-indol-3-yl)acetyl]-
• (2S)-2-[[2-(1H-indol-3-yl)acetyl]amino]butanedioicaci
• INDOLE-3-ACETYL-L-ASPARTIC ACID PLANT
• INDOLE-3-ACETYL-L-ASPARTIC ACID (IAAsp)
• (2S)-2-[[2-(1H-indol-3-yl)acetyl]amino]butanedioic acid
• Indole-3-acetyl-L-aspartic acid
• IAA-L-Asp

L-Aspartic acid, N-[2-(1H-indol-3-yl)acetyl]-

CAS: 2456-73-7

Formula: C₁₄H₁₄N₂O₅

Purity: 95%

Color and Shape: Solid

Molecular weight: 290.2714

Ref: IN-DA002OJV

(S)-2-(2-(1H-Indol-3-yl)acetamido)succinic acid

CAS: 2456-73-7

(S)-2-(2-(1H-Indol-3-yl)acetamido)succinic acid

Purity: 95%

Molecular weight: 290.28g/mol

Ref: 54-OR1054010

Indole 3-Aspartate-d7

CAS: 2456-73-7

Formula: C₁₄H₇D₇N₂O₅

Molecular weight: 297.32

Ref: 4Z-I-091030

Indole 3-Aspartate

CAS: 2456-73-7

Formula: C₁₄H₁₄N₂O₅

Molecular weight: 290.28

Ref: 4Z-I-091025

Indole-3-acetyl-L-aspartic acid

CAS: 2456-73-7

Indole-3-acetyl-L-aspartic acid, also known as 3IAA or IAA, is a naturally occurring amino acid. It is used in the study of plant physiology and serves as a substrate for ATP synthesis. 3IAA is synthesized from tryptophan by the enzyme indole acetyltransferase. The kinetic data obtained with 3IAA can be used to compare the effects of light exposure on ATP levels in plants. Indole-3-acetyl-L-aspartic acid inhibits cell growth and induces apoptosis, which may be due to its ability to inhibit protein synthesis by preventing RNA and DNA synthesis. This compound has been shown to have surface membrane inhibiting properties, which may be due to its ability to cross the plasma membrane.

Formula: C₁₄H₁₄N₂O₅

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 290.27 g/mol

Ref: 3D-FI30390

Indole-3-acetyl-L-aspartic Acid

CAS: 2456-73-7

Stability Hygroscopic
Applications Indole-3-acetyl-L-aspartic Acid is an indole-3-acetyl-amino acid conjugate involved in regulatory mechanisms for the control of auxin activity during physiological and pathophysiological responses.
References Ostrowski, M., et al.: J Plant Physiol, 191, 63-72 (2016)

Formula: C₁₄H₁₄N₂O₅

Color and Shape: Neat

Molecular weight: 290.27

Ref: TR-I577370