Molecular structure of Indole-3-acetone, CAS Number: 1201-26-9
Indole-3-acetone (CAS 1201-26-9)
Alternate Names:
1-(1H-Indol-3-yl)propan-2-one
CAS Number:
1201-26-9
Molecular Weight:
173.22
Molecular Formula:
C11H11NO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Indole-3-acetone is a derivative of indole, an aromatic heterocyclic compound found in a variety of plants, fungi, and bacteria. It has been found to have anti-inflammatory, anti-cancer, anti-oxidant, and anti-microbial properties. In addition, Indole-3-acetone has potential applications in the fields of biotechnology, drug discovery, and agricultural sciences. It has been used to control plant diseases and pests, as well as to produce a variety of enzymes, such as amylases, proteases, and lipases.
Indole-3-acetone (CAS 1201-26-9) References
- Putative receptor for the plant growth hormone auxin identified and characterized by anti-idiotypic antibodies. | Prasad, PV. and Jones, AM. 1991. Proc Natl Acad Sci U S A. 88: 5479-83. PMID: 11607194
- Expression of a single-chain antibody against indole-3-acetic acid in Escherichia coli. | Mitani, N. and Matsumoto, R. 2004. Biosci Biotechnol Biochem. 68: 1565-8. PMID: 15277762
- Auxin immunolocalization implicates vesicular neurotransmitter-like mode of polar auxin transport in root apices. | Schlicht, M., et al. 2006. Plant Signal Behav. 1: 122-33. PMID: 19521492
- Humic substances induce lateral root formation and expression of the early auxin-responsive IAA19 gene and DR5 synthetic element in Arabidopsis. | Trevisan, S., et al. 2010. Plant Biol (Stuttg). 12: 604-14. PMID: 20636903
- Levels of indole-3-acetic acid in intact and decapitated coleoptiles as determined by a specific and highly sensitive solid-phase enzyme immunoassay. | Weiler, EW., et al. 1981. Planta. 153: 561-71. PMID: 24275876
- Radioimmunoassay for pmol-quantities of indole-3-acetic acid for use with highly stable [(125)I]- and [ (3)H]IAA derivatives as radiotracers. | Weiler, EW. 1981. Planta. 153: 319-25. PMID: 24276936
- Effects of exogenous nutrients on polyketide biosynthesis in Escherichia coli. | Sun, L., et al. 2015. Appl Microbiol Biotechnol. 99: 693-701. PMID: 25411046
- Inhibition of indoleamine 2,3-dioxygenase and tryptophan 2,3-dioxygenase by beta-carboline and indole derivatives. | Eguchi, N., et al. 1984. Arch Biochem Biophys. 232: 602-9. PMID: 6431906
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Indole-3-acetone, 1 g | sc-279211 | 1 g | $80.00 | |||
Indole-3-acetone, 5 g | sc-279211A | 5 g | $208.00 |