Fenamic acid
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(Redirected from Fenamate)
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| Names | |
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| IUPAC name
2-(phenylamino)benzoic acid
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| Other names
N-phenylanthranilic acid
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| Identifiers | |
91-40-7  |
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| ChEBI | CHEBI:34756  |
| ChEMBL | ChEMBL23832 |
| ChemSpider | 4233 |
| ECHA InfoCard | 100.001.879 |
| 4182 | |
| Jmol 3D model | Interactive image |
| PubChem | 4386 |
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| Properties | |
| C13H11NO2 | |
| Molar mass | 213.23 g/mol |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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 verify (what is ?) |
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| Infobox references | |
Fenamic acid is a molecule which, especially in its ester form, fenamate,[1]:458 serves as a parent structure for several non-steroidal anti-inflammatory drugs, 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]
References[edit]
- ^ Gupta, PK. Drug NomenclatureUnited States Adopted Names. Ch 27 in Remington: The Science and Practice of Pharmacy, Vol 1. Eds. David B. Troy, Paul Beringer. Lippincott Williams & Wilkins, 2006 ISBN 9780781746731
- ^ a b Sriram D, Yogeeswari P. Medicinal Chemistry, 2nd Edition. Pearson Education India, 2010. ISBN 9788131731444
- ^ Auburn University course material. Jack DeRuiter, Principles of Drug Action 2, Fall 2002 1: Non-Steroidal Antiinflammatory Drugs (NSAIDS)
