Aurothioglucose

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Aurothioglucose
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Clinical data
Other namesGold thioglucose, Solganal, Auromyose
AHFS/Drugs.comConsumer Drug Information
Routes of
administration
Intramuscular injection
ATC code
Pharmacokinetic data
Bioavailability0%
Identifiers
  • gold(I) (2S,3S,4R,5S)-3,4,5-trihydroxy-
    6-(hydroxymethyl)-oxane-2-thiolate
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
E number{{#property:P628}}
CompTox Dashboard (EPA)
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Chemical and physical data
FormulaC6H11AuO5S
Molar mass392.18 g·mol−1
3D model (JSmol)
  • O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1S[Au]
  • InChI=1S/C6H12O5S.Au/c7-1-2-3(8)4(9)5(10)6(12)11-2;/h2-10,12H,1H2;/q;+1/p-1/t2-,3-,4+,5-,6-;/m1./s1 checkY
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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

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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In 2001, aurothioglucose was withdrawn from the Dutch market, where it had been the only injectable gold preparation available since 1943, forcing hospitals to change medication for a large number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

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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

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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

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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

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References

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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