Weight | 374.374 g/mol |
---|---|
Formula | C17H14N2O6S |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 2 |
Aromatic Rings | 3 |
Rotatable Bonds | 6 |
Iguratimod (123663-49-0)
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- Sigma-Aldrich - Search for Iguratimod
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- TCI - Iguratimod51.00 - 308.00 USD
- Efficacy and safety of iguratimod compared with placebo and salazosulfapyridine in active rheumatoid arthritis: a controlled, multicenter, double-blind, parallel-group study (Modern Rheumatology, 2007)
- A Novel Disease-Modifying Antirheumatic Drug, Iguratimod, Ameliorates Murine Arthritis by Blocking IL-17 Signaling, Distinct from Methotrexate and Leflunomide (Journal of Immunology, 2013)
- Safety and efficacy of combination therapy of iguratimod with methotrexate for patients with active rheumatoid arthritis with an inadequate response to methotrexate: An open-label extension of a randomized, double-blind, placebo-controlled trial (Modern Rheumatology, 2014)
- Effect of iguratimod and other anti-rheumatic drugs on adenocarcinoma colon 26-induced cachexia in mice (Inflammation Research, 2007)
- Long-term safety study of iguratimod in patients with rheumatoid arthritis (Modern Rheumatology, 2007)
- Efficacy of the clinical use of iguratimod therapy in patients with rheumatoid arthritis (Modern Rheumatology, 2015)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCS(=O)(=O)NC1=C(C=C2C(=C1)OC=C(C2=O)NC=O)OC3=CC=CC=C3
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- Pubchem - Iguratimod
- Wikipedia - iguratimod
Iguratimod is an anti-inflammatory drug for the treatment of rheumatoid arthritis. It is approved for use in China and Japan, and is sold by Eisai and Toyama Chemical. Its mechanism of action involves the suppression of nuclear factor-kappa B (NF-B).
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