https://en.m.wikipedia.org/wiki/Heterocyclic_compound

https://en.m.wikipedia.org/wiki/Carbanion

https://en.m.wikipedia.org/wiki/Methanol

https://en.m.wikipedia.org/wiki/Hydrogen_sulfide

https://www.bibliotecapleyades.net/salud/salud_miraclemineral07.htm

Dimethyl sulfoxide (DMSO) and methylsulfonylmethane (MSM) are chemically related substances.

Solvents:
Water Ethanol DMSO

DMSO
Dimethyl Sulfoxide

MSM (DMSO2)
Methylsulfonylmethane

DMSO: De-Proton-ated
Negative Hydrogen Bond

Lye:
Sodium Hydroxide
Potassium Hydroxide

Dimethyl:
Sugar Carbon Polymer

Methyl: (Acetone)
simplest hydrocarbon unit

Sulfoxide:
Sulfur

Dimethyl Sulfoxide
Methyl Sulfonyl Methane

Benzimidazoline
Polybenzimidazole

All commercially available MSM is synthetic and created through a chemical reaction of DMSO and hydrogen peroxide.

DMSO is produced using several starting materials: methanol and hydrogen sulfide, or methanol and carbon disulfide.

the process simply entails a treatment of wood chips with a mixture of sodium hydroxide and sodium sulfide, known as white liquor.

Escherichia coli metabolite and an alkylating agent.

DMSO
Magnesium Chloride
Vitamin D3
K2 MK7
Q10
Serrapeptase
Nattokinase

Quinone & DMSO molecules look very similar & do similar things as Enzymes to plaque & fibrosis.

it appears that enzyme stability is a issue, DMSO solvent will probably destroy the delicate chemical structure.

Aryl Aromatization of cyclohexanes and other aliphatic rings: reagents are catalysts used in hydrogenation such as platinum, palladium and nickel (reverse hydrogenation), quinones and the elements sulfur and selenium.

Aromatic, Quinone, Sulfur, Selenium, Iridium (Chloride)

Sulfur and Selenium: Oxidation State in Protein Structure and Function

cysteine,
methionine,
selenocysteine,
selenomethionine

Amino Acid > Enzime > Solvent

Sulfur
Selenium
Serine
Cysteine
Redox Chameleon

Sulfur and selenium occur in proteins as constituents of the amino acids cysteine, methionine, selenocysteine, and selenomethionine. Recent research underscores that these amino acids are truly exceptional. Their redox activity under physiological conditions allows an amazing variety of posttranslational protein modifications, metal free redox pathways, and unusual chalcogen redox states that increasingly attract the attention of biological chemists. Unlike any other amino acid, the “redox chameleon” cysteine can participate in several distinct redox pathways, including exchange and radical reactions, as well as atom‐, electron‐, and hydride‐transfer reactions. It occurs in various oxidation states in the human body, each of which exhibits distinctive chemical properties (e.g. redox activity, metal binding) and biological activity.

The position of selenium in the periodic table between the metals and the nonmetals makes selenoproteins ideal catalysts for many biological redox transformations.

https://www.onlinelibrary.wiley.com/doi/10.1002/anie.200300573

MSM is highly volatile and most of it is lost in the steam during cooking, steaming.

MSM gives up its sulfur to help the body to form amino acids methionine and cysteine collagen and keratin.

MSM (Methyl-Sulfonyl-Methane) is that it is similar in structure to Coenzyme Q-10.