For research use only. Not for therapeutic Use.
HTHQ (Cat No.: I001816) is a potent lipophilic phenolic antioxidant known for its strong antioxidant activity. It functions by directly reacting with reactive oxygen species (ROS), effectively scavenging them and forming more stable free radicals. This antioxidant property makes HTHQ valuable in various applications, particularly in combating oxidative stress and protecting cells and tissues from oxidative damage. Researchers often use it in studies related to oxidative stress and antioxidant mechanisms. If you need to, please contact us in time, and we will reply to you as soon as possible within 24 hours.
| Catalog Number | I001816 |
| CAS Number | 148081-72-5 |
| Molecular Formula | C15H24O2 |
| Purity | ≥95% |
| Target | NF-κB |
| Solubility | 10 mM in DMSO |
| Storage | 2-8°C |
| IUPAC Name | 4-hexoxy-2,3,6-trimethylphenol |
| InChI | InChI=1S/C15H24O2/c1-5-6-7-8-9-17-14-10-11(2)15(16)13(4)12(14)3/h10,16H,5-9H2,1-4H3 |
| InChIKey | ATMNQRRJNBCQJO-UHFFFAOYSA-N |
| SMILES | CCCCCCOC1=C(C(=C(C(=C1)C)O)C)C |
| Reference | </br>1:HTHQ (1-O-hexyl-2,3,5-trimethylhydroquinone), an anti-lipid-peroxidative compound: its chemical and biochemical characterizations. Hino T, Kawanishi S, Yasui H, Oka S, Sakurai H.Biochim Biophys Acta. 1998 Sep 16;1425(1):47-60. PMID: 9813237 </br>2:Inhibitory effects of 1-O-hexyl-2,3,5-trimethylhydroquinone (HTHQ), green tea catechins and other antioxidants on 2-amino-6-methyldipyrido[1,2-a:3/’,2/’-d]imidazole (Glu-P-1)-induced rat hepatocarcinogenesis and dose-dependent inhibition by HTHQ of lesion induction by Glu-P-1 or 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx). Hirose M, Hasegawa R, Kimura J, Akagi K, Yoshida Y, Tanaka H, Miki T, Satoh T, Wakabayashi K, Ito N, et al.Carcinogenesis. 1995 Dec;16(12):3049-55. PMID: 8603484 |
