Molecular structure of Gallacetophenone, CAS Number: 528-21-2
Gallacetophenone (CAS 528-21-2)
Alternate Names:
2′,3′,4′-Trihydroxyacetophenone
CAS Number:
528-21-2
Molecular Weight:
168.15
Molecular Formula:
C8H8O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
Gallacetophenone is an organic compound that occurs naturally in various plants and fruits. Extensive scientific investigations have been carried out on gallacetophenone to explore its potential applications. Despite ongoing studies, the precise mechanism of action of gallacetophenone remains incompletely understood. It is postulated that gallacetophenone may function as an antioxidant by scavenging free radicals and hindering cellular oxidative damage.
Gallacetophenone (CAS 528-21-2) References
- Inhibition of inducible nitric oxide synthase and cyclooxygenase-2 activity by 1,2,3,4,6-penta-O-galloyl-beta-D-glucose in murine macrophage cells. | Lee, SJ., et al. 2003. Arch Pharm Res. 26: 832-9. PMID: 14609132
- A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect. | Liu, X., et al. 2010. J Med Chem. 53: 8274-86. PMID: 21073191
- Simultaneous determination of ten bioactive compaounds from the roots of Cynanchum paniculatum by using high performance liquid chromatography coupled-diode array detector. | Weon, JB., et al. 2012. Pharmacogn Mag. 8: 231-6. PMID: 23060698
- Biological clues to potent DNA-damaging activities in food and flavoring. | Hossain, MZ., et al. 2013. Food Chem Toxicol. 55: 557-67. PMID: 23402862
- Co-catalytic oxidative coupling of primary amines to imines using an organic nanotube-gold nanohybrid. | Jawale, DV., et al. 2014. Chem Commun (Camb). 50: 15251-4. PMID: 25347761
- Analysis of avenanthramides in oat products and estimation of avenanthramide intake in humans. | Pridal, AA., et al. 2018. Food Chem. 253: 93-100. PMID: 29502849
- Biodegradation of 7-Hydroxycoumarin in Pseudomonas mandelii 7HK4 via ipso-Hydroxylation of 3-(2,4-Dihydroxyphenyl)-propionic Acid. | Krikštaponis, A. and Meškys, R. 2018. Molecules. 23: PMID: 30321993
- Tyrosinase-Targeting Gallacetophenone Inhibits Melanogenesis in Melanocytes and Human Skin-Equivalents. | Lee, JY., et al. 2020. Int J Mol Sci. 21: PMID: 32365630
- Integrative analyses of targeted metabolome and transcriptome of Isatidis Radix autotetraploids highlighted key polyploidization-responsive regulators. | Zhang, Z., et al. 2021. BMC Genomics. 22: 670. PMID: 34535080
- Comparison of dehydration methods for untreated lignin resole by hot air oven and vacuum rotary evaporator to synthesize lignin-based phenolic foam. | Suttaphakdee, P., et al. 2022. Heliyon. 8: e08769. PMID: 35079652
- Paeonia × suffruticosa (Moutan Peony)-A Review of the Chemical Composition, Traditional and Professional Use in Medicine, Position in Cosmetics Industries, and Biotechnological Studies. | Ekiert, H., et al. 2022. Plants (Basel). 11: PMID: 36501418
- Herb Robert's Gift against Human Diseases: Anticancer and Antimicrobial Activity of Geranium robertianum L. | Świątek, Ł., et al. 2023. Pharmaceutics. 15: PMID: 37242803
- Automated, rapid identification of bacteria by pattern analysis of growth inhibition profiles obtained with Autobac 1. | Buck, GE., et al. 1977. J Clin Microbiol. 6: 46-9. PMID: 407248
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Gallacetophenone, 5 g | sc-235241 | 5 g | $40.00 |