G6PD Deficiency
Glucose-6 Phosphate Dehydrogenase

Thiamine
5-Carbon
Pentose
Ribose
NADPH
Ribose 5-Phosphate
Thioester
Thioesterase
Disulfide
Glutathione

Garlic
Allicin
PARP
Poly ADP-Ribose Polymerase

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

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

Switching to the cyclic pentose phosphate pathway powers the oxidative burst in activated neutrophils

https://www.nature.com/articles/s42255-022-00550-8

NADPH—The Forgotten Reducing Equivalent

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168431/

Allicin, the Odor of Freshly Crushed Garlic: A Review of Recent Progress in Understanding Allicin’s Effects on Cells

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001868/

..

Thiamine
5-Carbon
Pentose
NADPH

charges

Glutathione

Sulfoxide Thioester
Reducing Agent
Decarboxylation
Simple Sugars

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https://en.m.wikipedia.org/wiki/Glucose-6-phosphate_dehydrogenase

https://en.m.wikipedia.org/wiki/Glucose-6-phosphate_dehydrogenase_deficiency

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

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

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Mannose: A Sweet Option in the Treatment of Cancer and Inflammation

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136145/

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Enzymatic Formulation Capable of Degrading Scrapie Prion under Mild Digestion Conditions

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712960/

Structure, Application, and Biochemistry of Microbial Keratinases

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8260994/

Keratinases can be understood as a class of proteases that are able to degrade keratin by cleaving the peptide bonds. Although the identified keratinases are serine and metalloproteases that are able to break the peptide bond in peptide chains, they recognize hydrophobic substrates and affect the disulfide bonds. Most keratinases require other enzymes to break the disulfide, and two steps, namely, keratin peptide releasing and peptide degradation are included in keratin degradation. Reduction reaction can be catalyzed by disulfide reductases or reducing agents.

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Effect of dentin biomodification techniques on the stability of the bonded interface

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8717850/

Effect of Dimethyl Sulfoxide on Bond Strength of a Self-Etch Primer and an Etch and Rinse Adhesive to Surface and Deep Dentin

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103470/

Thiazole: A Versatile Standalone Moiety Contributing to the Development of Various Drugs and Biologically Active Agents

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268695/

Metabolism of Sulfur-Containing Amino Acids: How the Body Copes with Excess Methionine, Cysteine, and Sulfide

https://www.sciencedirect.com/science/article/pii/S0022316622024233

Transsulfuration
https://www.sciencedirect.com/topics/medicine-and-dentistry/transsulfuration-pathway

Methylenetetrahydrofolate
Reductase
(MTHFR)

https://www.sciencedirect.com/topics/biochemistry-genetics-and-molecular-biology/methylenetetrahydrofolate-reductase

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https://en.m.wikipedia.org/wiki/1,2-Dithiolane

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Thiazine (Blue)
Thiazole (B1)

Dimethylaniline
Phenothiazine

Methylene blue, a bright greenish blue organic dye belonging to the phenothiazine family.

Methylene blue was discovered in 1876 and is manufactured by a process, introduced about 1886, using dimethylaniline as the principal starting material.

Phenothiazine, abbreviated PTZ, is an organic compound that has the formula S(C6H4)2NH and is related to the thiazine-class of heterocyclic compounds.

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

https://www.drugs.com/sfx/methylene-blue-side-effects.html

Transition metal-free synthesis and functionalization of phenothiazines

https://www.sciencedirect.com/science/article/abs/pii/S0040402023004209