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Aurothioglucose

CAS No.
12192-57-3
Chemical Name:
Aurothioglucose
Synonyms
gtg;GGT;GGT 1;brenol;oronol;aurotan;authron;romosol;D22S732;CS-1197
CBNumber:
CB4140009
Molecular Formula:
C6H11AuO5S
Molecular Weight:
392.18
MDL Number:
MFCD00056080
MOL File:
12192-57-3.mol
MSDS File:
SDS
Last updated:2023-05-18 11:31:13

Aurothioglucose Properties

Melting point >107oC (dec.)
storage temp. 2-8°C
solubility H2O: soluble5mg/mL, clear
form powder
color white to beige
Merck 13,887
Stability Hygroscopic, Light Sensitive
FDA UNII 2P2V9Q0E78
ATC code M01CB04
IARC 3 (Vol. 13, Sup 7) 1987
EPA Substance Registry System Aurothioglucose (12192-57-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H317-H412
Precautionary statements  P261-P272-P273-P280-P302+P352-P333+P313
Hazard Codes  Xn
Risk Statements  42/43
Safety Statements  22-36/37-45
RIDADR  2811
WGK Germany  3
HazardClass  6.1(b)
PackingGroup  III
HS Code  2843300000
Toxicity LD50 intravenous in chicken: 1gm/kg

Aurothioglucose price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SAB2701966 Anti-GGT1 antibody produced in rabbit 12192-57-3 100μL $496 2024-03-01 Buy
Sigma-Aldrich SAB1410523 Anti-GGT1 antibody produced in rabbit purified immunoglobulin, buffered aqueous solution 12192-57-3 100μg $524 2024-03-01 Buy
Sigma-Aldrich HPA065444 Anti-GGT1 antibody produced in rabbit Prestige Antibodies? Powered by Atlas Antibodies, affinity isolated antibody 12192-57-3 100μL $580 2024-03-01 Buy
Sigma-Aldrich A0606 Aurothioglucose hydrate ≥96% (titration) 12192-57-3 5mg $201 2024-03-01 Buy
Sigma-Aldrich 1045508 Aurothioglucose hydrate United States Pharmacopeia (USP) Reference Standard 12192-57-3 100mg $689 2024-03-01 Buy
Product number Packaging Price Buy
SAB2701966 100μL $496 Buy
SAB1410523 100μg $524 Buy
HPA065444 100μL $580 Buy
A0606 5mg $201 Buy
1045508 100mg $689 Buy

Aurothioglucose Chemical Properties,Uses,Production

Description

Aurothioglucose is highly water soluble, and its aqueous solutions decompose on long standing. It therefore is available as a suspension in sesame oil. Gold content is approximately 50%. Following IM injection, it is highly protein bound (95%), and peak plasma levels are achieved within 2 to 6 hours. Following a single 50-mg dose, the biological half-life ranges from 3 to 27 days, but following successive weekly doses, the half-life increases to 14 to 40 days after the third dose. The therapeutic effect does not correlate with serum plasma gold levels but appears to depend on total accumulated gold. Aurothioglucose is indicated for the adjunctive treatment of adult and juvenile rheumatoid arthritis.

Chemical Properties

yellow crystals,

History

In 1927, aurothioglucose was found to relieve joint pain when used to treat bacterial endocarditis. The area of chrysotherapy had begun. Subsequent investigations led to an extensive study of gold compounds in Great Britain by the Empire Rheumatism Council, which reported in 1961 that sodium aurothiomalate was effective in slowing the development of progressive joint diseases. Both aurothioglucose and sodium aurothiomalate are orally ineffective and are administered by IM injection. In 1985, the first orally effective gold compound for arthritis, auranofin, was introduced in the United States. Several other gold compounds have been evaluated clinically but do not appear to offer advantages in terms of efficacy or toxicity.

Uses

Aurothioglucose hydrate has been used in redox stress survival assay in human cell lines and for inducing obese phenotype in mice.

Uses

To produce obesity in experimental animals.

brand name

Solganal (Schering, USA, Yugoslavia), Aureotan (BYK Gulden, Germany).

Biochem/physiol Actions

Aurothioglucose, a gold compound used clinically to treat rheumatoid arthritis, has recently been found to be a potent PKCiota-Par6 interaction inhibitor, with an IC50 approximately 1 μM. Disruption of this interaction disrupts a rac1 signaling pathway that is required for transformed growth in non-small-cell lung cancer.

Clinical Use

Aurothioglucose is highly water soluble, and its aqueous solutions decompose on long standing. It therefore is available as a suspension in sesame oil. Gold content is approximately 50%. Following IM injection, it is highly protein bound (95%), and peak plasma levels are achieved within 2 to 6 hours. Following a single 50-mg dose, the biological half-life ranges from 3 to 27 days, but following successive weekly doses, the half-life increases to 14 to 40 days after the third dose. The therapeutic effect does not correlate with serum plasma gold levels but appears to depend on total accumulated gold. Aurothioglucose is indicated for the adjunctive treatment of adult and juvenile rheumatoid arthritis.

Safety Profile

Confirmed carcinogen with experimental carcinogenic and neoplastigenic data. A deadly human poison by an unspecified route. An experimental poison by intramuscular route. Moderately toxic by subcutaneous and intravenous routes. Human systemic effects: nausea or vomiting, cholestatic jaundlce, and eye effects. An experimental teratogen. Other experimental reproductive effects. See also GOLD COMPOUNDS. When heated to decomposition it emits very toxic fumes of SOx. Used to treat rheumatoid arthritis.

Synthesis

Synthesis: gold thioglucose is prepared by adding a solution of gold bromide to an aqueous solution of thioglucose that contains sulfur dioxide. After heating, the product is precipitated by the addition of ethanol.
Aurothioglucose synthesis

Purification Methods

Purify it by dissolving it in H2O (0.05g in 1mL) and precipitating it by adding EtOH. It yields yellow crystals with a slight mercaptan odour. It decomposes slowly in H2O, and is soluble in propylene glycol but insoluble in EtOH and other common organic solvents. [Caterson & Taylor FEBS Lett 98 351 1979, Cooney et al. Biochem J 259 651 1989.]

Dosage

Aurothioglucose is an antirheumatic used to treat active progressing rheumatoid arthritis and nondisseminated lupus erythematosus. The drug is administered at weekly intervals by intramuscular injection (10 mg, 25 mg, then 50 mg) until 800 mg to 1 g has been given. If improvement takes place, the drug is then administered at levels that balance the urinary excretion of gold. During this maintenance therapy the interval between injections is lengthened to 3 – 4 weeks.

Aurothioglucose Preparation Products And Raw materials

Raw materials

Preparation Products

Aurothioglucose Suppliers

Global( 62)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21688 55
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49391 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33350 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
DONBOO AMINO ACID COMPANY
+8613063595538 donboo@donboo.com China 9365 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9823 79

View Lastest Price from Aurothioglucose manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	Aurothioglucose pictures 2020-01-10 Aurothioglucose
12192-57-3
US $1.00 / KG 1g 98% 200kgs Career Henan Chemical Co
(1-d-glucosylthio)gold (1-thio-d-glucopyranosato)-gol (d-glucopyranosylthio)-gol (d-glucopyranosylthio)gold 1-aurothio-d-glucopyranose 1-thio-d-glucopyranose,goldcomplex 1-thio-d-glucopyranose,monogold(1+)salt 1-thio-glucopyranose,monogold(1+)salt aureotan auromyose aurotan aurothioglucose aurumine authron brenol glysanolb goldthioglucose gtg oronol romosol skf10056 solganal solganalb SODIUMAUROTHIOGLUCOSE Gold, [1-(thio-.kappa.S)-D-glucopyranosato-.kappa.O2]- AUROTHIOGLUCOSE USP Aurothioglucose hydrate Gold thioglucose, Solganal, Solganol (a-D-Glucopyranosylthio)gold 1-Deoxy-1-[aurio(I)thio]-D-glucopyranose Aurio(I)-1-thio-D-glucopyranoside (1-THIO-D-GLUCOPYRANOSATO)GOLD (alpha-D-glucopyranosylthio)gold Aurothioglucose (100 mg) Solganol Anti-GGT1 antibody produced in rabbit D22S732 GGT GGT 1 Gold, [1-(thio-κS)-D-glucopyranosato-κO2]- Aurothioglucose, Gold thioglucose CS-1197 Aurothioglucose 80% 12192-57-3 Aurothioglucose 12192-57-3 C6H11AuO5S AuC6H12O5S AuC6H10O5S AuC6H11O5S BioChemical Cell Signaling and Neuroscience Cell Biology Protein Kinase C (PKC) Kinase/Phosphatase Biology Serine/Threonine Kinase Inhibitors Organometallics