General Information of Metabolite (ID: MT063)
  Meta Name
Hydrogen peroxide (H2O2)
  Unify Name
Hydrogen peroxide
  Synonym    Click to Show/Hide the Detailed Synonyms of This Metabolite
[OH(OH)];Dihydrogen dioxide;H2O2;HOOH;Oxydol;Perhydrol;Adeka super el;Albone;Albone 35;Albone DS;Anti-keim 50;Asepticper;Baquashock;CIX;Clarigel gold;Crestal whitestrips;Crystacide;Dentasept;Deslime LP;Hioxyl;Hipox;Hybrite;Hydrogen dioxide;Inhibine;Lase peroxide;Lensan a;Magic bleaching;Metrokur;Mirasept;Nite white excel 2;Odosat D;Opalescence xtra;Oxigenal;Oxyfull;Oxysept;Oxysept I;Pegasyl;Perone;Peroxaan;Peroxclean;Quasar brite;Select bleach;Superoxol;T-Stuff;Whiteness HP;Whitespeed;Xtra white;Hydrogen peroxide (H2O2);Hydroperoxide;Peroxide, hydrogen;
  Molecule Type
Other metabolites
  Formula
H2O2
  Inchi Key
MHAJPDPJQMAIIY-UHFFFAOYSA-N
  Description    Click to Show/Hide the Detailed Description of This Metabolite
Human Metabolome Database (HMDB): Hydrogen peroxide (H2O2) is a very pale blue liquid which appears colourless in a dilute solution, slightly more viscous than water. It is a weak acid. It has strong oxidizing properties and is therefore a powerful bleaching agent that is mostly used for bleaching paper, but has also found use as a disinfectant and as an oxidizer. Hydrogen peroxide in the form of carbamide peroxide is widely used for tooth whitening (bleaching), both in professionally- and in self-administered products. Hydrogen peroxide (H2O2) is a well-documented component of living cells. It plays important roles in host defense and oxidative biosynthetic reactions. In addition there is growing evidence that at low levels, H2O2 also functions as a signaling agent, particularly in higher organisms. H2O2 has increasingly been viewed as an important cellular signaling agent in its own right, capable of modulating both contractile and growth-promoting pathways with more far-reaching effects. Due to the accumulation of hydrogen peroxide in the skin of patients with the depigmentation disorder vitiligo, the human epidermis cannot have the normal capacity for autocrine synthesis, transport and degradation of acetylcholine as well as the muscarinic (m1-m5) and nicotinic signal transduction in keratinocytes and melanocytes. Accumulating evidence suggests that hydrogen peroxide (H(2)O(2)) plays an important role in cancer development. Experimental data have shown that cancer cells produce high amounts of H(2)O(2). An increase in the cellular levels of H(2)O(2) has been linked to several key alterations in cancer, including DNA alterations, cell proliferation, apoptosis resistance, metastasis, angiogenesis and hypoxia-inducible factor 1 (HIF-1) activation. (PMID: 17150302, 17335854, 16677071, 16607324, 16514169).
  External Links   HMDB ID   HMDB0003125
  VMH ID   h2o2
  KEGG ID   C00027

The epigenetic modification information of this metabolite
Modification Type Molecule EM Info Cell/Tissue Type Modified sites Condition REF
Histone Dephosphorylation H3 EM Info A549 cells serine 10 . [1]
Histone Acetylation H3 EM Info BEAS-2B cells lysine 8 . [1], [2]
Histone Methylation H3 EM Info BEAS-2B cells lysine 27 . [1], [2]
Histone Methylation H3 EM Info BEAS-2B cells lysine 4 . [1], [2]
Histone Methylation H3 EM Info BEAS-2B cells lysine 9 . [1], [2]

The microbes that produce this metabolite
      Streptococcus pneumoniae
         Detailed Information MIC Info click to show the detail information of this Microbiota [1]
         Description
Streptococcus pneumoniae, or pneumococcus, is a facultative anaerobic, gram-positive, alpha-hemolytic or beta-hemolytic member of the genus Streptococcus. They are usually found in pairs and do not form spores and are nonmotile. As a significant human pathogenic bacteria S. pneumoniae was recognized as a major cause of pneumonia.

References
1 Streptococcus pneumoniae Infection Promotes Histone H3 Dephosphorylation by Modulating Host PP1 Phosphatase. Cell Rep. 2020 Mar 24;30(12):4016-4026.e4. doi: 10.1016/j.celrep.2020.02.116.
2 Oxidative stress alters global histone modification and DNA methylation. Free Radic Biol Med. 2015 May;82:22-8. doi: 10.1016/j.freeradbiomed.2015.01.028. Epub 2015 Feb 3.

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