2-hATQ

For research use only. Not for therapeutic Use.

  • CAT Number: I020827
  • CAS Number: 605-32-3
  • Molecular Formula: C14H8O3
  • Molecular Weight: 224.21
  • Purity: 98%
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2-hATQ(Cat No.:I020827), is a chemical compound known as 2-hydroxy-3-amino-1,4-naphthoquinone. It belongs to the naphthoquinone family and exhibits diverse properties. 2-hATQ has been investigated for its antioxidant and antibacterial activities, making it a subject of interest in pharmaceutical research. Additionally, it serves as a valuable starting material for the synthesis of various compounds. With its unique structure containing hydroxy and amino groups, 2-hATQ offers potential for further exploration in medicinal chemistry and other scientific disciplines to unlock its therapeutic and functional potential.


Catalog Number I020827
CAS Number 605-32-3
Synonyms

2-hATQ; 2 hATQ; 2-Hydroxyanthraquinone; 2 Hydroxyanthraquinone; 2-hydroxy-9,10-Anthraquinone; β-Hydroxyanthraquinone; β Hydroxyanthraquinone; NSC 2595; NSC2595; NSC-2595;

Molecular Formula C14H8O3
Purity 98%
Target Disease Research Fields
Solubility To be determined
Appearance Solid powder
Storage Room Temperature
IUPAC Name 2-hydroxyanthracene-9,10-dione
InChI InChI=1S/C14H8O3/c15-8-5-6-11-12(7-8)14(17)10-4-2-1-3-9(10)13(11)16/h1-7,15H
InChIKey GCDBEYOJCZLKMC-UHFFFAOYSA-N
SMILES O=C1C2=C(C=CC=C2)C(C3=CC(O)=CC=C13)=O
Reference

1: Butterworth BE, Mathre OB, Ballinger KE, Adalsteinsson O. Contamination is a frequent confounding factor in toxicology studies with anthraquinone and related compounds. Int J Toxicol. 2004;23(5):335-44. doi: 10.1080/10915810490517072. PMID: 15513832.
2: Mallakin A, McConkey BJ, Miao G, McKibben B, Snieckus V, Dixon DG, Greenberg BM. Impacts of structural photomodification on the toxicity of environmental contaminants: anthracene photooxidation products. Ecotoxicol Environ Saf. 1999 Jun;43(2):204-12. doi: 10.1006/eesa.1999.1764. PMID: 10375423.
3: Ramamoorthy S, Mudgal G, Rajesh D, Nawaz Khan F, Vijayakumar V, Rajasekaran C. Characterisation of novel pH indicator of natural dye Oldenlandia umbellata L. Nat Prod Res. 2009;23(13):1210-7. doi: 10.1080/14786410802696635. PMID: 19731140.
4: Shi Y, Wang CH, Gong XG. Apoptosis-inducing effects of two anthraquinones from Hedyotis diffusa WILLD. Biol Pharm Bull. 2008 Jun;31(6):1075-8. doi: 10.1248/bpb.31.1075. PMID: 18520033.
5: Tikkanen L, Matsushima T, Natori S. Mutagenicity of anthraquinones in the Salmonella preincubation test. Mutat Res. 1983 Mar;116(3-4):297-304. doi: 10.1016/0165-1218(83)90067-8. PMID: 6339896.
6: Hilgert I, Cudlín J, Steinerová N, Vanĕk Z. Antitumour and immunosuppressive activity of hydroxyanthraquinones and their glucosides. Folia Biol (Praha). 1977;23(2):99-109. PMID: 863051.

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