Molecular structure of 2-Aminoanthraquinone, CAS Number: 117-79-3
2-Aminoanthraquinone (CAS 117-79-3)
Application:
2-Aminoanthraquinone is used in fabrication of high performance electrode of supercapacitor based on chemically modified graphene hydrogel
CAS Number:
117-79-3
Purity:
≥80%
Molecular Weight:
223.23
Molecular Formula:
C14H9NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
2-Aminoanthraquinone (2-AAQ) represents an organic compound classified as an anthraquinone derivative. It manifests as a colorless solid and exhibits solubility in most organic solvents. In scientific research, 2-Aminoanthraquinone has been employed across a range of applications. It acts as a fluorescent probe for detecting metal ions in aqueous solutions, a fluorescent dye for DNA detection, and a reagent for polymer synthesis. Notably, 2-Aminoanthraquinone functions as a potent inhibitor of the enzyme cytochrome P450 2C9 (CYP2C9).
2-Aminoanthraquinone (CAS 117-79-3) References
- Nephrotoxic effect of 2-aminoanthraquinone in Fischer rats. | Baker, JR., et al. 1975. J Toxicol Environ Health. 1: 1-11. PMID: 1185814
- Bioassay of 2-aminoanthraquinone for possible carcinogenicity. | ,. 1978. Natl Cancer Inst Carcinog Tech Rep Ser. 144: 1-117. PMID: 12799718
- Influence of functional group substitutions on the carcinogenicity of anthraquinone in rats and mice: analysis of long-term bioassays by the National Cancer Institute and the National Toxicology Program. | Doi, AM., et al. 2005. J Toxicol Environ Health B Crit Rev. 8: 109-26. PMID: 15804751
- High-performance supercapacitor electrodes based on graphene hydrogels modified with 2-aminoanthraquinone moieties. | Wu, Q., et al. 2011. Phys Chem Chem Phys. 13: 11193-8. PMID: 21562653
- Study on the interaction mechanism of 2-aminoanthraquinone with calf thymus DNA. | Yang, H., et al. 2013. J Biochem Mol Toxicol. 27: 272-8. PMID: 23606275
- Synthesis, docking and biological activities of novel hybrids celecoxib and anthraquinone analogs as potent cytotoxic agents. | Almutairi, MS., et al. 2014. Int J Mol Sci. 15: 22580-603. PMID: 25490139
- In vitro antimalarial and xanthine oxidase inhibition of 2-Aminoanthraquinone. | Rauf, A., et al. 2016. Pak J Pharm Sci. 29: 429-32. PMID: 27087090
- In Situ Growth and Wrapping of Aminoanthraquinone Nanowires in 3 D Graphene Framework as Foldable Organic Cathode for Lithium-Ion Batteries. | Yang, G., et al. 2017. ChemSusChem. 10: 3419-3426. PMID: 28722277
- Alterations in drug-metabolizing enzymes during feeding of the carcinogen 2-aminoanthraquinone. | Ramanathan, R., et al. 1981. Toxicol Appl Pharmacol. 60: 204-12. PMID: 6792748
- Protection by testosterone propionate against the nephrotoxicity of 2-aminoanthraquinone in Fischer rats. | Gothoskar, SV. and Weisburger, EK. 1980. Med Biol. 58: 281-4. PMID: 7206834
- Hepatic vitamin A status of rats during feeding of the hepatocarcinogen 2-aminoanthraquinone. | Reddy, TV. and Weisburger, EK. 1980. Cancer Lett. 10: 39-44. PMID: 7226128
- Proteinuria in the Fischer rat by feeding 2-aminoanthraquinone. | Gothoskar, SV., et al. 1980. Med Biol. 58: 337-40. PMID: 7230915
- Centromere analysis of micronuclei induced by 2-aminoanthraquinone in cultured mouse splenocytes using both a gamma-satellite DNA probe and anti-kinetochore antibody. | Afshari, AJ., et al. 1994. Environ Mol Mutagen. 24: 96-102. PMID: 7925332
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Aminoanthraquinone, 25 g | sc-223430 | 25 g | $122.00 |