Molecular structure of 2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid, CAS Number: 6266-66-6
2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid (CAS 6266-66-6)
CAS Number:
6266-66-6
Molecular Weight:
293.33
Molecular Formula:
C18H15NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid (IOPB) is a member of the indole-3-carboxylic acid family, which are found in various plants and animals. In vitro studies have demonstrated that 2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid has anti-inflammatory, analgesic, and anti-cancer properties. It inhibits the activity of the enzyme cyclooxygenase-2 (COX-2), which is involved in the regulation of inflammation and pain. In addition, 2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid may act to inhibit the growth of cancer cells in vitro.
2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid (CAS 6266-66-6) References
- Induction of jasmonic acid biosynthetic genes inhibits Arabidopsis growth in response to low boron. | Huang, Y., et al. 2021. J Integr Plant Biol. 63: 937-948. PMID: 33289292
- Integrative Roles of Phytohormones on Cell Proliferation, Elongation and Differentiation in the Arabidopsis thaliana Primary Root. | Zluhan-Martínez, E., et al. 2021. Front Plant Sci. 12: 659155. PMID: 33981325
- Cotton miR393-TIR1 Module Regulates Plant Defense Against Verticillium dahliae via Auxin Perception and Signaling. | Shi, G., et al. 2022. Front Plant Sci. 13: 888703. PMID: 35592575
- RALF1 peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis. | Li, L., et al. 2022. Proc Natl Acad Sci U S A. 119: e2121058119. PMID: 35878023
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-(1H-Indol-3-yl)-4-oxo-4-phenyl-butyric acid, 500 mg | sc-304510 | 500 mg | $550.00 |