Aurothioglucose
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| Clinical data | |
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| Other names | Gold thioglucose, Solganal, Auromyose |
| AHFS/Drugs.com | Consumer Drug Information |
| Routes of administration | Intramuscular injection |
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| Bioavailability | 0% |
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| E number | {{#property:P628}} |
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| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C6H11AuO5S |
| Molar mass | 392.18 g·mol−1 |
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Aurothioglucose, also known as gold thioglucose, is a chemical compound with the formula AuSC6H11O5. This derivative of the sugar glucose was formerly used to treat rheumatoid arthritis.[1]
History
[edit | edit source]Throughout history, gold was used to cure diseases, although the efficacy was not established. In 1935, gold drugs were reported to be effective for the treatment of rheumatoid arthritis.[2] Although many patients reacted positively to the drug, gold thioglucose was not uniformly effective.
Only one gold drug remains in active clinical use for this purpose in the United States: auranofin, sodium aurothiomalate (gold sodium thiomalate) and aurothioglucose were discontinued by their manufacturers in 2019 due to gold shortages, and the rising cost of gold.[3][4]
In 2001, aurothioglucose was withdrawn from the Dutch market, where it had been the only injectable gold preparation available since 1943, forcing hospitals to change medication for a large number of patients to aurothiomalate.[5] The drug had been in use for more than 70 years, and four years later the reasons for its sudden disappearance remained unclear.[6]
It was discontinued from the US market in 2019, along with sodium aurothiomalate,[7] leaving only generic Auranofin as the only gold salt on the US market.[3][8]
Medicinal chemistry
[edit | edit source]Gold thioglucose features gold in the oxidation state of +I, like other gold thiolates. It is a water-soluble, non-ionic species that is assumed to exist as a polymer.[2] Under physiological conditions, an oxidation-reduction reaction leads to the formation of metallic gold and sulfinic acid derivative of thioglucose.[1]
- 2 AuSTg → 2 Au + TgSSTg
- TgSSTg + H2O → TgSOH + TgSH
- 2 TgSOH → TgSO2H + TgSH
- Overall: 2 H2O + 4 AuSTg → 4 Au + TgSO2H + 3 TgSH
(where AuSTg = gold thioglucose, TgSSTg = thioglucose disulfide, TgSO2H = sulfinic acid derivative of thioglucose)
Preparation
[edit | edit source]Gold thioglucose can be prepared by treating gold bromide with thioglucose solution saturated with sulfur dioxide. Gold thioglucose is precipitated with methanol and recrystallized with water and methanol.
Miscellaneous observations
[edit | edit source]In recent research, it was found that injection of gold thioglucose induces obesity in mice.[9] Aurothioglucose has an interaction with the antimalarial medication hydroxychloroquine.[1]
See also
[edit | edit source]References
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External links
[edit | edit source]Error creating thumbnail: File missing Media related to Lua error in Module:Commons_link at line 62: attempt to index field 'wikibase' (a nil value). at Wikimedia Commons