| Identification | Back Directory | [Name]
Tryptophan, N-indol-3-ylacetyl- (6CI) | [CAS]
57105-53-0 | [Synonyms]
Indole-3-acetyl-L-tryptopha
N-(3-Indolylacetyl)-L-tryptophan
INDOLE-3-ACETYL-L-TRYPTOPHAN (IATrp)
Tryptophan, N-indol-3-ylacetyl- (6CI)
(2-(1H-Indol-3-yl)acetyl)-L-tryptophan
L-Tryptophan, N-[2-(1H-indol-3-yl)acetyl]-
(S)-2-(2-(1H-indol-3-yl)acetamido)-3-(1H-indol-3-yl)propanoic acid | [Molecular Formula]
C21H19N3O3 | [MDL Number]
MFCD18641983 | [MOL File]
57105-53-0.mol | [Molecular Weight]
361.39 |
| Chemical Properties | Back Directory | [Melting point ]
181-183 °C | [Boiling point ]
767.2±60.0 °C(Predicted) | [density ]
1.399±0.06 g/cm3(Predicted) | [solubility ]
DMSO: Sparingly soluble: 1-10 mg/ml
Ethanol: Slightly soluble: 0.1-1 mg/ml | [pka]
3?+-.0.10(Predicted) |
| Hazard Information | Back Directory | [Uses]
Indole-3-acetyl-L-tryptophan is an indole-3-acetyl-amino acid conjugate involved in regulatory mechanisms for the control of auxin activity during physiological and pathophysiological responses. It may also be used in the synthesis of β-D-galactosidase and β-D-glucosidase inhibitors. | [References]
[1] C S FEUNG R O M R H Hamilton. Metabolism of Indole-3-acetic Acid: IV. Biological Properties of Amino Acid Conjugates.[J]. Plant Physiology, 1977, 59 1: 91-93. DOI: 10.1104/pp.59.1.91
[2] STASWICK P E. The tryptophan conjugates of jasmonic and indole-3-acetic acids are endogenous auxin inhibitors.[J]. Plant Physiology, 2009: 1310-1321. DOI: 10.1104/pp.109.138529 |
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