Weight | 678.491 g/mol |
---|---|
Formula | C20H34AuO9PS |
Hydrogen Acceptors | 10 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 8 |
AURANOFIN (34031-32-8)
Ridaura · SK and F-39162 · SK and F 39162
Score:
#642 in Biochemistry
,
#1820 in Biology
,
#2176 in Chemistry
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- Auranofin therapy and quality of life in patients with rheumatoid arthritis. Results of a multicenter trial (The American Journal of Medicine, 1986)
- Inhibition of thioredoxin reductase by auranofin induces apoptosis in cisplatin-resistant human ovarian cancer cells (Free Radical Biology and Medicine, 2007)
- Evaluation of the in Vivo Antitumor Activity and in Vitro Cytotoxic Properties of Auranofin, a Coordinated Gold Compound, in Murine Tumor Models (Cancer Research, 1985)
- Comparison of auranofin, gold sodium thiomalate, and placebo in the treatment of rheumatoid arthritis (Arthritis & Rheumatism, 1983)
- Auranofin. New oral gold compound for treatment of rheumatoid arthritis. (Annals of the Rheumatic Diseases, 1976)
- Synthesis and structural characterisation of linear Au(I) N-heterocyclic carbene complexes: New analogues of the Au(I) phosphine drug Auranofin (Journal of Organometallic Chemistry, 2005)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ridaura
- SK and F-39162
- SK and F 39162
- Crisinor
- Ridauran
- SK and F D 39162
- SK and F39162
-
SMILESCCP(CC)CC.CC(=O)OCC1C(C(C(C(O1)[S-])OC(=O)C)OC(=O)C)OC(=O)C.[Au+]
-
InChIKeyAUJRCFUBUPVWSZ-UHFFFAOYSA-M
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Synthesis
ACETYL CHLORIDE
+
Reactant
(O-acylation)
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