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  2. Testosterone propionate/testosterone phenylpropionate ...

    en.wikipedia.org/wiki/Testosterone_propionate/...

    30 mg testosterone propionate [1] 60 mg testosterone phenylpropionate [1] 60 mg testosterone isocaproate [1] 100 mg testosterone decanoate [1] Cumulatively, a 1 ml of the oil solution contains exactly 250 mg of above mentioned testosterone esters. [2] [3] This particular numerical value is clearly depicted in the name of the product, Sustanon ...

  3. Glutathione - Wikipedia

    en.wikipedia.org/wiki/Glutathione

    Glutathione (GSH, / ˌ ɡ l uː t ə ˈ θ aɪ oʊ n /) is an organic compound with the chemical formula HOCOCH(NH 2)CH 2 CH 2 CONHCH(CH 2 SH)CONHCH 2 COOH. It is an antioxidant in plants , animals , fungi , and some bacteria and archaea .

  4. Terbinafine - Wikipedia

    en.wikipedia.org/wiki/Terbinafine

    This accumulation results in therapeutic levels of terbinafine even after 80 days following one week treatment of 250 mg/day. Different dosing schedules have been proposed such as 500 mg/day for one week or 250 mg/day for two weeks each followed by a drug-free period of two or three weeks, totaling 3 months of treatment including the drug-free ...

  5. Glutathione synthetase - Wikipedia

    en.wikipedia.org/wiki/Glutathione_synthetase

    Glutathione synthetase (GSS) (EC 6.3.2.3) is the second enzyme in the glutathione (GSH) biosynthesis pathway. It catalyses the condensation of gamma-glutamylcysteine and glycine, to form glutathione. [2] Glutathione synthetase is also a potent antioxidant. It is found in many species including bacteria, yeast, mammals, and plants. [3]

  6. Glutathione S-transferase - Wikipedia

    en.wikipedia.org/wiki/Glutathione_S-transferase

    The glutathione binding site, or "G-site", is located in the thioredoxin-like domain of both cytosolic and mitochondrial GSTs. The region containing the greatest amount of variability between the assorted classes is that of helix α2 , where one of three different amino acid residues interacts with the glycine residue of glutathione.

  7. Microsomal glutathione S-transferase 1 - Wikipedia

    en.wikipedia.org/wiki/Microsomal_glutathione_S...

    Other family members, demonstrating glutathione S-transferase and peroxidase activities, are involved in cellular defense against toxic, carcinogenic, and pharmacologically active electrophilic compounds. This gene encodes a protein that catalyzes the conjugation of glutathione to electrophiles

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