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Clinical data | |
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Trade names | Norvedan |
AHFS/Drugs.com | International Drug Names |
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ECHA InfoCard | 100.038.129 ![]() |
Chemical and physical data | |
Formula | C17H12ClNO2S |
Molar mass | 329.80 g·mol−1 |
3D model (JSmol) | |
Melting point | 162–163 °C (324–325 °F) |
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Fentiazac is a thiazole-based nonsteroidal anti-inflammatory drug (NSAID) developed for use in joint and muscular pain.[1] Like most other NSAIDs, it acts through inhibition of prostaglandin synthesis, via non-selective inhibition of both COX-1 and COX-2. First described in 1974, it was synthesized using the Hantzsch thiazole synthesis.[2]
Fentiazac was marketed under the trade-name Norvedan (among others), but its market status is currently unknown and assumed to be discontinued.[3]
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pyrazolones / pyrazolidines |
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salicylates |
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acetic acid derivatives and related substances |
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oxicams |
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propionic acid derivatives (profens) |
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n-arylanthranilic acids (fenamates) |
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COX-2 inhibitors (coxibs) |
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other |
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NSAID combinations |
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Key: underline indicates initially developed first-in-class compound of specific group; #WHO-Essential Medicines; †withdrawn drugs; ‡veterinary use. | |
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Anti-inflammatory preparations, non-steroids |
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Capsaicin derivatives |
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Other |
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