3602-55-9
3602-55-9
Chemical Structure
2-tert-Butyl-1,4-benzoquinone
- CAS No.: 3602-55-9
- Formula:C10H12O2
- Molecular Weight:164.20
IUPAC Name: 2-(tert-butyl)cyclohexa-2,5-diene-1,4-dione
InChIKey: NCCTVAJNFXYWTM-UHFFFAOYSA-N
SMILES: CC(C)(C1=CC(C=CC1=O)=O)C
Biological Activity: 2-tert-Butyl-1,4-benzoquinone is a food additive oxidant, an electrophilic metabolite of Butylated hydroxyanisole (HY-B1066), and an antibacterial agent. 2-tert-Butyl-1,4-benzoquinone reduces virulence factors, activates Nrf2, and induces S-arylation of its negative regulator Keap1. 2-tert-Butyl-1,4-benzoquinone induces HO-1. 2-tert-Butyl-1,4-benzoquinone exhibits quorum sensing inhibitory activity against Chromobacterium violaceum[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-tert-Butyl-1,4-benzoquinone | 99.34% | 2-tert-Butyl-1,4-benzoquinone is a food additive oxidant, an electrophilic metabolite of Butylated hydroxyanisole (HY-B1066), and an antibacterial agent. 2-tert-Butyl-1,4-benzoquinone reduces virulence factors, activates Nrf2, and induces S-arylation of its negative regulator Keap1. 2-tert-Butyl-1,4-benzoquinone induces HO-1. 2-tert-Butyl-1,4-benzoquinone exhibits quorum sensing inhibitory activity against Chromobacterium violaceum. | ||||||||||||||||||||
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2,6-Diisopropyl-p-benzoquinone (Standard) | ≥98% | 2,6-Diisopropyl-p-benzoquinone (Standard) is the analytical standard of 2,6-Diisopropyl-p-benzoquinone. This product is intended for research and analytical applications. | ||||||||||||||||||||
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Ketoisophorone | 99.90% | Ketoisophorone (4-Oxoisophorone) is the active small molecule that can be used as building block. | ||||||||||||||||||||
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Piperitenone | 95.0% | Piperitenone is a terpenoid, and exhibits antioxidant activity. Piperitenone scavenges DPPH free radicals with an IC50 of 22.7 μg/mL, and inhibits the peroxidation of linoleic acid. | ||||||||||||||||||||
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Thymoquinone | 99.80% | Thymoquinone is an orally active natural product isolated from N. sativa Thymoquinone down-regulates the VEGFR2-PI3K-Akt pathway. Thymoquinone has antioxidant, anti-inflammatory, anticancer, antiviral, anticonvulsant, antifungal, antiviral, antiangiogenic activity and hepatoprotective effects. Thymoquinone can be used to study Alzheimer's disease, cancer, cardiovascular disease, infectious disease and inflammation . | ||||||||||||||||||||
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Toluquinone | Toluquinone is a Toluquinol analogue. Toluquinone shows lower growth inhibitory activity against a panel of cancer cell lines of breast adenocarcinoma, promyelocytic leukemia, glioblastoma, fibrosarcoma, and colorectal adenocarcinoma than Toluquinol. | |||||||||||||||||||||
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2,6-Dimethylbenzoquinone | 99.36% | 2,6-Dimethylbenzoquinone (2,6-DMBQ) is a benzoquinone derivative. 2,6-Dimethylbenzoquinone promotes Photosystem II-mediated photoelectrochemical water oxidation via electron transfer between spinach chloroplast Photosystem II membranes and carbon paste electrodes, and accepts electrons from Photosystem II during oxygen evolution assays. 2,6-Dimethylbenzoquinone undergoes direct photolysis in aqueous solution under 365 nm conditions, producing 2,6-dimethylhydroquinone and 3-hydroxy-2,6-dimethylbenzoquinone. | ||||||||||||||||||||
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2,5-Dimethyl-1,4-benzoquinone | 99.35% | 2,5-Dimethyl-1,4-benzoquinone is a jack bean urease (HY-P2767) inhibitor (IC50: 0.98 μM). 2,5-Dimethyl-1,4-benzoquinone can be used in the study of soil urease activity in agriculture. | ||||||||||||||||||||
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Trimethylbenzoquinone | 99.87% | Trimethylbenzoquinone (Compound 5) is a methylated benzoquinone. Trimethylbenzoquinone exhibits moderate cytotoxicity against K562 cells, with its IC50 being 0.75 μM. Trimethylbenzoquinone is completely unable to cause inter-strand DNA cross-linking and cannot alkylate DNA guanines. Trimethylbenzoquinone can be used to study the relationship between the nitrogen heterocyclic group and DNA cross-linking. | ||||||||||||||||||||
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Duroquinone | 99.85% | Duroquinone (Tetramethylquinone) is a model compound of amphiphilic quinone, which can be used as an oxidative-reductive activity probe. Duroquinone can be easily reduced by biological systems to hydrogen peroxide (DQH₂) or semi-quinone free radicals (DQ•⁻). Duroquinone can freely pass through the cell membrane, facilitating the study of the electron transfer process inside and outside the cells. Duroquinone can be used to investigate the relationship between metabolism in the pulmonary circulation and endothelial cells. | ||||||||||||||||||||
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References
- [1]. Xu K Z, et al. 2-tert-Butyl-1, 4-benzoquinone, a food additive oxidant, reduces virulence factors of Chromobacterium violaceum[J]. Lwt, 2022, 163: 113569.
- [2]. Abiko Y, et al. Interaction of Keap1 modified by 2-tert-butyl-1,4-benzoquinone with GSH: evidence for S-transarylation. Chem Res Toxicol. 2013 Jul 15;26(7):1080-7. [Content Brief]
