mephenytoin

chemical compound
ChemicalSubstance type_of_chemical_entity Q1175385
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mephenytoin

Summary

mephenytoin is a type of chemical entity[1]. mephenytoin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]

Key Facts

  • mephenytoin's instance of is recorded as type of chemical entity[3].
  • mephenytoin's chemical structure is recorded as Mephenytoin.svg[4].
  • mephenytoin's physically interacts with is recorded as Sodium voltage-gated channel alpha subunit 5[5].
  • mephenytoin's physically interacts with is recorded as Sodium voltage-gated channel alpha subunit 4[6].
  • mephenytoin's physically interacts with is recorded as Sodium voltage-gated channel alpha subunit 10[7].
  • mephenytoin's physically interacts with is recorded as Sodium voltage-gated channel alpha subunit 9[8].
  • mephenytoin's physically interacts with is recorded as Sodium voltage-gated channel alpha subunit 3[9].
  • mephenytoin's physically interacts with is recorded as Sodium voltage-gated channel alpha subunit 2[10].
  • mephenytoin's physically interacts with is recorded as sodium voltage-gated channel alpha subunit 1[11].
  • mephenytoin's physically interacts with is recorded as Sodium voltage-gated channel alpha subunit 11[12].
  • mephenytoin's CAS Registry Number is recorded as 50-12-4[13].
  • mephenytoin's EC number is recorded as 200-012-8[14].
  • mephenytoin's canonical SMILES is recorded as CCC1(C(=O)N(C(=O)N1)C)C2=CC=CC=C2[15].
  • mephenytoin's InChI is recorded as InChI=1S/C12H14N2O2/c1-3-12(9-7-5-4-6-8-9)10(15)14(2)11(16)13-12/h4-8H,3H2,1-2H3,(H,13,16)[16].
  • mephenytoin's InChIKey is recorded as GMHKMTDVRCWUDX-UHFFFAOYSA-N[17].
  • mephenytoin's ATC code is recorded as N03AB04[18].
  • mephenytoin's chemical formula is recorded as C₁₂H₁₄N₂O₂[19].
  • mephenytoin's subclass of is recorded as chemical compound[20].
  • mephenytoin's has use is recorded as medication[21].
  • mephenytoin's Commons category is recorded as Mephenytoin[22].
  • mephenytoin's MeSH descriptor ID is recorded as D008617[23].
  • mephenytoin's ChEMBL ID is recorded as CHEMBL861[24].
  • mephenytoin's Guide to Pharmacology Ligand ID is recorded as 7223[25].
  • mephenytoin's Freebase ID is recorded as /m/0bjn4g[26].
  • mephenytoin's UNII is recorded as R420KW629U[27].

Why It Matters

mephenytoin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2] mephenytoin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] mephenytoin is known by 3 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] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  4. [6] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  5. [7] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  6. [8] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  7. [9] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [10] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  9. [11] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  10. [12] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  11. [13] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  12. [14] . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . DrugBank. wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . ChEMBL. Retrieved . wikidata.org.
  23. [25] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . Global Substance Registration System. Retrieved . 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). mephenytoin. Retrieved May 3, 2026, from https://4ort.xyz/entity/mephenytoin
MLA “mephenytoin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mephenytoin.
BibTeX @misc{4ortxyz_mephenytoin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{mephenytoin}}, year = {2026}, url = {https://4ort.xyz/entity/mephenytoin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): mephenytoin — https://4ort.xyz/entity/mephenytoin (retrieved 2026-05-03)

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