cephalothin

chemical compound
ChemicalSubstance type_of_chemical_entity Q2736126
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cephalothin

Summary

cephalothin is a type of chemical entity[1]. cephalothin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2]

Key Facts

  • cephalothin's instance of is recorded as type of chemical entity[3].
  • cephalothin's physically interacts with is recorded as Solute carrier family 22 member 8[4].
  • cephalothin's physically interacts with is recorded as Solute carrier family 22 member 11[5].
  • cephalothin's canonical SMILES is recorded as CC(=O)OCC1=C(N2C(C(C2=O)NC(=O)CC3=CC=CS3)SC1)C(=O)O[6].
  • cephalothin's chemical formula is recorded as C₁₆H₁₆N₂O₆S₂[7].
  • cephalothin is a type of chemical compound[8].
  • cephalothin is used for medication[9].
  • cephalothin's Commons category is recorded as Cefalotin[10].
  • cephalothin's MCN code is recorded as 3003.20.51[11].
  • cephalothin's MCN code is recorded as 3004.20.51[12].
  • cephalothin's isomeric SMILES is recorded as CC(=O)OCC1=C(N2C@@HSC1)C(=O)OC@@HSC1)C(=O)O">[13].
  • cephalothin's mass is recorded as {'unit': 'Q483261', 'amount': '+396.045'}[14].
  • cephalothin's medical condition treated is recorded as gram-negative bacterial infection[15].
  • cephalothin's medical condition treated is recorded as upper respiratory tract infection[16].
  • cephalothin's medical condition treated is recorded as urinary tract infection[17].
  • cephalothin's medical condition treated is recorded as Escherichia coli infectious disease[18].
  • cephalothin's medical condition treated is recorded as staphylococcal infection[19].
  • cephalothin's subject has role is recorded as enzyme inhibitor[20].
  • cephalothin's subject has role is recorded as antibiotic[21].
  • cephalothin's subject has role is recorded as bactericide[22].
  • cephalothin's stereoisomer of is recorded as (6R,7S)-3-(acetyloxymethyl)-8-oxo-7-[(1-oxo-2-thiophen-2-ylethyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid[23].
  • cephalothin's pregnancy category is recorded as Australian pregnancy category A[24].
  • cephalothin's pregnancy category is recorded as US pregnancy category B[25].
  • cephalothin's defined daily dose is recorded as {'unit': 'Q41803', 'amount': '+4'}[26].
  • cephalothin's WHO Aware Classification is recorded as access[27].

Why It Matters

cephalothin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2] cephalothin has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[28] cephalothin is known by 27 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  3. [5] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . PubChem. Retrieved . wikidata.org.
  12. [14] . PubChem. Retrieved . wikidata.org.
  13. [15] . NDF-RT. Retrieved . wikidata.org.
  14. [16] . NDF-RT. Retrieved . wikidata.org.
  15. [17] . NDF-RT. Retrieved . wikidata.org.
  16. [18] . NDF-RT. Retrieved . wikidata.org.
  17. [19] . NDF-RT. Retrieved . wikidata.org.
  18. [20] . NDF-RT. Retrieved . wikidata.org.
  19. [21] . Medical Subject Headings. Retrieved . wikidata.org.
  20. [22] . ChEBI. wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . whocc.no. whocc.no. Provenance: wikidata.org.
  25. [27] . 2023 ‎AWaRe classification‎. 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). cephalothin. Retrieved May 3, 2026, from https://4ort.xyz/entity/cephalothin
MLA “cephalothin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cephalothin.
BibTeX @misc{4ortxyz_cephalothin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cephalothin}}, year = {2026}, url = {https://4ort.xyz/entity/cephalothin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cephalothin — https://4ort.xyz/entity/cephalothin (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/cephalothin · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 27d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Chembl id CHEMBL617
    Probes and drugs id PD010018
    Guide to pharmacology ligand id
    Unii
    + 111 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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