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Names | |
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Preferred IUPAC name
2-Anilinobenzoic acid | |
Other names
N-phenylanthranilic acid
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Identifiers | |
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3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider |
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ECHA InfoCard | 100.001.879 ![]() |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C13H11NO2 | |
Molar mass | 213.23 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Fenamic acid is an organic compound, which, especially in its ester form, is called fenamate.[1]: 458 serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including mefenamic acid, tolfenamic acid, flufenamic acid, and meclofenamic acid. These drugs are commonly referred to as "anthranilic acid derivatives" or "fenamates" because fenamic acid is a derivative of anthranilic acid.[2]: 235 [3]: 17 [2]
Fenamic acid can be synthesized from 2-chlorobenzoic acid and can be converted into acridone.[4]
pyrazolones / pyrazolidines | |
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salicylates | |
acetic acid derivatives and related substances | |
oxicams |
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propionic acid derivatives (profens) |
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n-arylanthranilic acids (fenamates) | |
COX-2 inhibitors (coxibs) | |
other | |
NSAID combinations | |
Key: underline indicates initially developed first-in-class compound of specific group; #WHO-Essential Medicines; †withdrawn drugs; ‡veterinary use. | |
Receptor (ligands) |
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Enzyme (inhibitors) | |||||||||||||||||
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