mefenamic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q284321
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mefenamic acid

Summary

mefenamic acid is a type of chemical entity[1]. It ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (304 views/month).[2]

Key Facts

  • mefenamic acid's instance of is recorded as type of chemical entity[3].
  • mefenamic acid's chemical structure is recorded as Mefenamic acid2DACS.svg[4].
  • mefenamic acid's physically interacts with is recorded as Prostaglandin-endoperoxide synthase 1[5].
  • mefenamic acid's physically interacts with is recorded as Prostaglandin-endoperoxide synthase 2[6].
  • mefenamic acid's physically interacts with is recorded as Potassium voltage-gated channel subfamily Q member 1[7].
  • mefenamic acid's physically interacts with is recorded as Transient receptor potential cation channel subfamily M member 3[8].
  • mefenamic acid's CAS Registry Number is recorded as 61-68-7[9].
  • mefenamic acid's EC number is recorded as 200-513-1[10].
  • mefenamic acid's canonical SMILES is recorded as CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C[11].
  • mefenamic acid's InChI is recorded as InChI=1S/C15H15NO2/c1-10-6-5-9-13(11(10)2)16-14-8-4-3-7-12(14)15(17)18/h3-9,16H,1-2H3,(H,17,18)[12].
  • mefenamic acid's InChIKey is recorded as HYYBABOKPJLUIN-UHFFFAOYSA-N[13].
  • mefenamic acid's ATC code is recorded as M01AG01[14].
  • mefenamic acid's chemical formula is recorded as C₁₅H₁₅NO₂[15].
  • mefenamic acid's subclass of is recorded as fenamates[16].
  • mefenamic acid's has use is recorded as medication[17].
  • mefenamic acid's Commons category is recorded as Mefenamic acid[18].
  • mefenamic acid's MeSH descriptor ID is recorded as D008528[19].
  • mefenamic acid's ChEMBL ID is recorded as CHEMBL686[20].
  • mefenamic acid's Guide to Pharmacology Ligand ID is recorded as 2593[21].
  • mefenamic acid's PDB structure ID is recorded as 4G2Z[22].
  • mefenamic acid's PDB structure ID is recorded as 3R43[23].
  • mefenamic acid's PDB structure ID is recorded as 4JQA[24].
  • mefenamic acid's PDB structure ID is recorded as 2XN3[25].
  • mefenamic acid's PDB structure ID is recorded as 5IKR[26].
  • mefenamic acid's Freebase ID is recorded as /m/04hf1v[27].

Why It Matters

mefenamic acid ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (304 views/month).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] It is known by 19 alternative names across languages and contexts.[29]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  8. [10] . Global Substance Registration System. Retrieved . wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . PubChem. Retrieved . wikidata.org.
  12. [14] . DrugBank. wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . ChEMBL. Retrieved . wikidata.org.
  19. [21] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  20. [22] . Protein Data Bank. Retrieved . wikidata.org.
  21. [23] . Protein Data Bank. Retrieved . wikidata.org.
  22. [24] . Protein Data Bank. Retrieved . wikidata.org.
  23. [25] . Protein Data Bank. Retrieved . wikidata.org.
  24. [26] . Protein Data Bank. Retrieved . wikidata.org.
  25. [27] . Freebase Data Dumps. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). mefenamic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/mefenamic-acid
MLA “mefenamic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mefenamic-acid.
BibTeX @misc{4ortxyz_mefenamic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{mefenamic acid}}, year = {2026}, url = {https://4ort.xyz/entity/mefenamic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): mefenamic acid — https://4ort.xyz/entity/mefenamic-acid (retrieved 2026-05-03)

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