Indole-3-acetamide
Indole-3-acetamide structure
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Common Name | Indole-3-acetamide | ||
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| CAS Number | 879-37-8 | Molecular Weight | 174.199 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 407.1±47.0 °C at 760 mmHg | |
| Molecular Formula | C10H10N2O | Melting Point | 148-150 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 200.0±29.3 °C | |
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Determination of urinary cortisol, cortisone and 6-sulfatoxymelatonin using dilute and shoot ultra-high pressure liquid chromatography-tandem mass spectrometry.
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 978-979 , 18-23, (2015) Human sleep is a natural part of every individual's life. Clear relationship between sleep and endocrine system has been already established. In particular, melatonin and cortisol are known to affect and regulate sleep/wake patterns. Here we report the develo... |
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Immunohistochemical observation of indole-3-acetic acid at the IAA synthetic maize coleoptile tips.
Plant Signal Behav. 6(12) , 2013-22, (2011) To investigate the distribution of IAA (indole-3-acetic acid) and the IAA synthetic cells in maize coleoptiles, we established immunohistochemistry of IAA using an anti-IAA-C-monoclonal antibody. We first confirmed the specificity of the antibody by comparing... |
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Structure of the flavoprotein tryptophan 2-monooxygenase, a key enzyme in the formation of galls in plants.
Biochemistry 52(15) , 2620-6, (2013) The flavoprotein tryptophan 2-monooxygenase catalyzes the oxidative decarboxylation of tryptophan to yield indole-3-acetamide. This is the initial step in the biosynthesis of the plant growth hormone indole-acetic acid by bacterial pathogens that cause crown ... |
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Partial purification of an enzyme hydrolyzing indole-3-acetamide from rice cells.
J. Plant Res. 117(3) , 191-8, (2004) The activity of indole-3-acetamide (IAM) hydrolase from rice cells was enriched ca. 628-fold by gel filtration and anion exchange column chromatography. The molecular masses of the IAM hydrolase estimated by gel filtration and sodium dodecyl sulfate polyacryl... |
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Many roads lead to "auxin": of nitrilases, synthases, and amidases.
Plant Biol. (Stuttg.) 8(3) , 326-33, (2006) Recent progress in understanding the biosynthesis of the auxin, indole-3-acetic acid (IAA) in Arabidopsis thaliana is reviewed. The current situation is characterized by considerable progress in identifying, at the molecular level and in functional terms, ind... |
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Translocator protein (18 kDa) as a pharmacological target in adipocytes to regulate glucose homeostasis.
Biochem. Pharmacol. 97 , 99-110, (2015) As a major regulator in obesity and its associated metabolic complications, the proper functioning of adipocytes is crucial for health maintenance, thus serving as an important target for the development of anti-obese and anti-diabetic therapies. There is inc... |
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Indole derivatives produced by the fungus Colletotrichum acutatum causing lime anthracnose and postbloom fruit drop of citrus.
FEMS Microbiol. Lett. 226(1) , 23-30, (2003) Postbloom fruit drop (PFD) of citrus and Key lime anthracnose (KLA) are caused by Colletotrichum acutatum. Both fungal isolates can infect flower petals, induce young fruit abscission and result in severe yield loss on many citrus cultivars. Previous studies ... |
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A simple method for simultaneous RP-HPLC determination of indolic compounds related to bacterial biosynthesis of indole-3-acetic acid.
Antonie van Leeuwenhoek 103 , 683-91, (2013) In this short technical report, we present a fast and simple procedure for sample preparation and a single-run Reversed Phase High Performance Liquid Chromatography (RP-HPLC) determination of seven indoles (indole-3-acetic acid, indole-3-acetamide, indole-3-a... |
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Structural studies on ligand-DNA systems: A robust approach in drug design.
J. Biosci. 37(3) , 553-61, (2012) Molecular docking, molecular mechanics, molecular dynamics and relaxation matrix simulation protocols have been extensively used to generate the structural details of ligand-receptor complexes in order to understand the binding interactions between the two en... |
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The translocator protein (18 kDa): central nervous system disease and drug design.
J. Med. Chem. 52 , 581-92, (2009)
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