Shareef, T. H. Mohamed Ahadu team published research in International Journal of Pharmaceutical Investigation in 2022 | 533-73-3

533-73-3, Benzene-1, 2, 4-triol, also known as hydroxyhydroquinone or 1, 2, 4-benzenetriol, belongs to the class of organic compounds known as hydroxyquinols and derivatives. Hydroxyquinols and derivatives are compounds containing a 1, 2, 4-trihydroxybenzene moiety. Benzene-1, 2, 4-triol is soluble (in water) and a very weakly acidic compound (based on its pKa). Outside of the human body, benzene-1, 2, 4-triol can be found in tea. This makes benzene-1, 2, 4-triol a potential biomarker for the consumption of this food product.
Benzene-1,2,4-triol is a benzenetriol carrying hydroxy groups at positions 1, 2 and 4. It has a role as a mouse metabolite.
1,2,4-Benzenetriol is a metabolite of benzene.
1,2,4-Benzenetriol is an intermediary metabolite of benzene that is present in roasted coffee beans. It is mutagenic and it causes cleaving of DNA single strands by the generation of reactive oxygen species.
1,2,4-Benzenetriol is a reactive molecule that has been shown to have hydrogen bonding interactions with copper chloride. It has been proposed as an inhibitor of methyltransferase, which is involved in the synthesis of methionine. Studies have shown that 1,2,4-Benzenetriol can also inhibit iron homeostasis and transfer reactions. The x-ray diffraction data for this compound shows that it forms a complex with the hydroxyl group. This complex is stabilized by hydrogen bonding interactions with the hydroxylic proton of the 1,2,4-benzenetriol molecule. 1,2,4-Benzenetriol has been shown to be toxic to HL-60 cells and K562 cells at concentrations greater than 5 mM. It has also been found to be effective against chlorogenic acids and other compounds in energy metabolism studies at concentrations between 0.5 and 2 mM., Safety of Benzene-1,2,4-triol

In general, the hydroxyl group makes alcohols polar. 533-73-3, formula is C6H6O3, Because of hydrogen bonding, alcohols tend to have higher boiling points than comparable hydrocarbons and ethers. Safety of Benzene-1,2,4-triol

Shareef, T. H. Mohamed Ahadu;Masood, Mohamed Divan research published 《 Phytochemical and molecular docking studies on indigenous herbs Glycyrrhiza glabra, Terminalia chebula and Hamdard joshanda》, the research content is summarized as follows. Glycyrrhiza glabra, Terminalia chebula and Hamdard joshanda is used as a traditional home medicine in developing countries that is easily available for a lesser cost with no side effects. These medicine decoctions made record in pandemic that have found efficacious in Covid-19 patients with RTI in addition to Dengue and Malarial fever. Our study aimed to explore the qual. as well as quant. in potential traditional medicines such as Glycyrrhiza glabra, Terminalia chebula and Hamdard joshanda through phytochem. and GC-MS anal. technique were conducted for finding all the potential chem. constituents in these herbal medicines. Docking studies were carried out between Glycyrrhiza glabra, Terminalia chebula and Hamdard joshanda and receptors of the crystal structure of SARS coronavirus, Lung Cancer and Mycobacterium tuberculosis proteins. The presence of various phytochems., total phenolic and flavonoid content were determined in Glycyrrhiza glabra, Terminalia chebula and Hamdard joshanda by standard procedure. Docking study was investigated using the crystal structure of SARS coronavirus protease for the modeling (PDB ID: 3SN8), Lung Cancer Protein for the modeling (PDB ID: 6JZ0) and Mycobacterium tuberculosis protein for the modeling (PDB ID: 4FDO). GC-MS chromatogram showed 26, 18 and 23 peaks that revealed 26, 18 and 23 phytoconstituents present in Glycyrrhiza glabra, Terminalia chebula, and Hamdard joshanda resp. Total phenolic and flavonoid contents found in Glycyrrhiza glabra, Terminalia chebula, and Hamdard joshanda were 1.95, 1.88, 1.55, and 0.66, 0.56, 0.49 mg/mL, resp. Docking studies were exhibited that moderate to higher efficacy against Covid-19, Tuberculosis and Lung cancer. However, several more in vivo and in vitro research needs to investigate their mol. system or any other significance of unused bioactive substance in these traditional medicines used for human relapse. These potential traditional medicines have been confirmed to be safe for human consumption and the present study would also suggest its direct consumption as well as for attaining the proven benefits.

533-73-3, Benzene-1, 2, 4-triol, also known as hydroxyhydroquinone or 1, 2, 4-benzenetriol, belongs to the class of organic compounds known as hydroxyquinols and derivatives. Hydroxyquinols and derivatives are compounds containing a 1, 2, 4-trihydroxybenzene moiety. Benzene-1, 2, 4-triol is soluble (in water) and a very weakly acidic compound (based on its pKa). Outside of the human body, benzene-1, 2, 4-triol can be found in tea. This makes benzene-1, 2, 4-triol a potential biomarker for the consumption of this food product.
Benzene-1,2,4-triol is a benzenetriol carrying hydroxy groups at positions 1, 2 and 4. It has a role as a mouse metabolite.
1,2,4-Benzenetriol is a metabolite of benzene.
1,2,4-Benzenetriol is an intermediary metabolite of benzene that is present in roasted coffee beans. It is mutagenic and it causes cleaving of DNA single strands by the generation of reactive oxygen species.
1,2,4-Benzenetriol is a reactive molecule that has been shown to have hydrogen bonding interactions with copper chloride. It has been proposed as an inhibitor of methyltransferase, which is involved in the synthesis of methionine. Studies have shown that 1,2,4-Benzenetriol can also inhibit iron homeostasis and transfer reactions. The x-ray diffraction data for this compound shows that it forms a complex with the hydroxyl group. This complex is stabilized by hydrogen bonding interactions with the hydroxylic proton of the 1,2,4-benzenetriol molecule. 1,2,4-Benzenetriol has been shown to be toxic to HL-60 cells and K562 cells at concentrations greater than 5 mM. It has also been found to be effective against chlorogenic acids and other compounds in energy metabolism studies at concentrations between 0.5 and 2 mM., Safety of Benzene-1,2,4-triol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts